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Practice with Taxonomy

worksheet

Though Next Generation Science Standards does not emphasize the memorizing of major groups anymore, students can benefit from learning the basics of how animals are classified. Taxonomy is often introduced with evolution, where students learn how to analyze phylogenetic trees and create cladograms .

This worksheet is a simple reinforcement exercise that covers the six kingdoms and the classification system developed by Carolus Linnaeus. I teach my students to learn this system with the mnemonic “ K ing P hilip C ame O ver F or G reat S oup” though there are many other versions. Each letter corresponds with a level of classification: Kingdom, Phylym, Class, Order, Family Genus, Species. You can add “darling” to the front of the sentence if you also want to include DOMAIN.

What I’ve found is that students can memorize this sequence, but they struggle with the actual concepts. Many will not be able to explain why there are more individual species within a class than there are within an order. Hierarchies can be difficult. I often uses boxes of varies sizes to show how each level fits into the next one.

My slides for classification are shown below. They are Google slides and can be edited if you make a copy.

Shannan Muskopf

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Biology LibreTexts

1.7: Assignment- Visualizing Taxonomy

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Open Pedagogy Assignments are assignments in which students use their agency and creativity to create knowledge artifacts that can support their own learning, their classmates’ learning, and the learning of students around the world. (See this peer-reviewed article for more details.) The assignment on this page is aligned to a learning outcome of Biology for Non-Majors I and we’ve identified the module where the reading appears. The assignment can be created with basic web and computing tools, a cell phone camera or any video recording device, Google or Word documents, and your learning management system.

Learning Objectives

  • Explain how relationships are indicated by the binomial naming system

In the introductory module on defining biology and applying its principles, we provide a general overview of how and why biologists study life. For this assignment, you are going to reflect upon how biologists organize and classify the different forms of life so that we can better understand them.

The product of your work may help future students to learn about some of the most difficult concepts in the course. Thus, think of your audience as friends who are taking Biology for Nonmajors in the next term. Your objective is to help them understand the classification systems that biologists use by visualizing the concept.

First , choose an organism to identify using biological taxonomy. This can be any plant or animal that you find interesting, peculiar, or from your experience. Think again about the future students who may be seeing your visualization: can you select an organism from your local environment or that has particular meaning from students that attend your institution?

Second , identify the scientific name in binomial nomenclature of the organism, as well as the series of classifications that make up the taxonomic hierarchy for your organism. According to the system proposed by Carl Linnaeus there are eight taxons, listed here from the broadest to the most specific:

Third , how would you visualize this organism’s taxonomy? Someone viewing the visualization should be able to understand hierarchical or nested relationships of the taxonomic groupings. You can use any means you wish to make your original visualization: draw, collage, digital illustration, video, slideshow, and so on. A successful visualization will include clear and accurate labels.

Lastly , share the visualization with your instructor. After grading and with your permission, your visualization may appear in future sections of the course to improve other students’ learning!

A Note To Teachers: The first time your students complete this assignment, choose the best ones, and ask students for permission to include them in future sections. Just post the visualizations in the appropriate module in the LMS. The idea is to have students generate content that other students can learn from in this assignment.

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Hands-on Activities for Teaching Biology to High School and Middle School Students

  • Hands-on Biology Activities

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  • biological molecules
  • cell structure and function
  • cellular respiration and photosynthesis
  • cell division and genetics
  • molecular biology
  • evolution and ecology
  • human physiology .

The expression "hands-on, minds-on" summarizes the philosophy we have incorporated in these activities - namely, that students will learn best if they are actively engaged and if their activities are closely linked to understanding important biological concepts. 

Most of our activities support the  Next Generation Science Standards (NGSS). 

Additional resources for teaching biology are available at Minds-on Activities for Teaching Biology .  These teaching resources include remote ready analysis and discussion activities , games, and overviews of important biological topics, including major concepts, common misconceptions, and suggested learning activities. We encourage you to  subscribe to our listserv  to receive notices when we  post new activities or significantly improved versions  of current activities.

We invite general comments in this comments section. If you have comments on specific activities, please use the links above to get to the comments section for each activity.  We welcome suggestions for other teachers, including useful preparatory or follow-up activities, additional resources, any questions you have, or a brief description of any problem you might have encountered.

If you would prefer to send your comments or questions in a private message, please write Ingrid Waldron at [email protected] .

Claudia's picture

As a first year IB Biology teacher in Australia, I am very grateful for all of Ingrid's hands-on, minds-on activities. I love how they link to real-world scenarios, add meaning and foster critical thinking. Thank you so much!

MH's picture

I am a public high school science teacher, and I've used many of your materials. When I need something new, I often go to your site first because you have such high-quality, hands-on, minds-on, NGSS-aligned activities.

Thank you for creating these resources and for making them free. These resources are needed and much appreciated!

Cheryl Ann Hollinger's picture

I've been a big fan of your Serendip Studio resources for years! I've used many of your activities in my Biology and my AP Biology classes. Your site is always one of the top 3 that I mention to other Biology teachers when they ask for recommendations of great websites. Thank you so much for your dedication to Biology education.

Kristen's picture

I am a high school Biology teacher and have been for ten years. I just wanted to thank you for making your amazing materials so accessible. It is very rare to find activities that are so accurate and comprehensive. I rarely need to modify the activities but it is helpful to be able to given the word document format. Thank you! Thank you! Thank you!

Jonathan 's picture

I am training to be science teacher and will graduate next year (2015) and I find very helpful in retrieving your lab practicals. I have retrieved many and hope it will help me much in my teaching career. Thank you very much you producing this practicals.

Dan's picture

Science and PBL

Hi! I am the Chair of Science of an alternative learning school that focuses on Project Based Learning Curriculum. This is by far and away the best website that I have ever seen, in all of my years of teaching, for Science PBL Tasks. Thank you very much for your assistance. And please notify me of updates.

Dee Bowen's picture

Biology. AP Biology, Forensic, Anatomy

I teach four HS sciences and found your activities to be a wonderful addition to my curriculum in all four areas! They provide excellent reinforcement and depth to the content we are studying. Your activities truly help the students learn and have saved me a lot of time in preparation. I highly recommend these activities. THANK YOU and well done.

Jessica G's picture

This is my first year teaching Biology, and as I work to incorporate more meaningful labs into my curriculum, your site has been so very valuable! I especially appreciate how your labs include the scientific method so thoroughly and allow for student design of experiments! Also thank you for providing the word documents to allow teachers like me to edit the labs to fit our specific groups of students! Keep up the good work!

Ricardo Azpiroz's picture

I am a Community College instructor on the prowl for activities and resources to incorporate into our Intro Biology lab. I have found wonderful stuff here and have used the Sockosome Meiosis activity with great success.

I do have a question: What is your policy regarding distribution of printed materials? I would like to incorporate some of your content into a lab manual to post online for our students to access. This would save them money and save us the hassle of dealing with publishers and the college bookstore. The copyright to our current manual is owned by the publisher (though we created it) so we need to come up with new material. What are your terms of use?

Ricardo Azpiroz, PhD Richland College Dallas, TX

iwaldron's picture

Using our material in an online lab manual

Dear Ricardo,

We are happy to learn that you have found our material useful.

If you want to post some of our materials in a lab manual on a website with access restricted to students in your courses, you are free to use any of our material, provided you acknowledge the source, including authors and website.

If you want to post any of our materials in a lab manual on a website with public access, we request that, instead of copying our material, you provide a brief explanation with a link to the relevant part of the Serendip website.

Please let me know if you would like any additional information.

Ingrid Waldron, Ph.D.

Department of Biology University of Pennsylvania

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Download minds-on activities for teaching biology.

Introduction and Activities Listing

biology classification assignment

Intro and Biological Molecules

  • Characteristics of Life
  • Levels of Organization in Biology  (NGSS)
  • Introduction to Proteins and DNA  (NGSS)
  • Enzymes Help Us Digest Food (NGSS; hands-on)
  • A Scientific Investigation – What types of food contain starch and protein? (NGSS; hands-on)
  • Coronaviruses – Introduction (NGSS)
  • Who Took Jerell’s iPod? -- An Organic Compound Mystery (hands-on)
  • Is Yeast Alive? (hands-on)
  • Macromolecules Jeopardy

Cell

Cell Structure and Function

  • Cell Structure and Function – Major Concepts and Learning Activities
  • Introduction to Cells (NGSS)
  • Structure and Function of Cells, Organs and Organ Systems (NGSS)
  • Why do some plants grow in odd shapes? (NGSS)
  • Introduction to Osmosis (NGSS; hands-on)
  • Cell Membrane Structure and Function (NGSS; hands-on)
  • Cell Vocabulary Review Game

biology classification assignment

Cellular Respiration and Photosynthesis

  • Cellular Respiration and Photosynthesis - Key Concepts and Activities
  • How do organisms use energy?  (NGSS)
  • Using Models to Understand Cellular Respiration (NGSS)
  • Using Models to Understand Photosynthesis  (NGSS)
  • Photosynthesis, Cellular Respiration and Plant Growth (NGSS; hands-on)
  • Food, Energy and Body Weight  (NGSS)
  • How do muscles get the energy they need for athletic activity?  (NGSS)
  • Alcoholic Fermentation in Yeast – A Bioengineering Design Challenge  (NGSS; hands-on)
  • Photosynthesis and Cellular Respiration  (NGSS)
  • Where does a tree’s mass come from?  (NGSS)
  • Photosynthesis Investigation  (NGSS; hands-on)

Cell Division

Cell Division

  • Mitosis and the Cell Cycle (NGSS; hands-on)
  • Mitosis and the Cell Cycle (NGSS)
  • Meiosis and Fertilization – Understanding How Genes Are Inherited (NGSS; hands-on)
  • Understanding How Genes are Inherited via Meiosis and Fertilization (NGSS)
  • Comparing Mitosis and Meiosis
  • What causes melanoma and other types of cancer? (NGSS)
  • Mistakes in Meiosis – Down Syndrome or Embryo Death (NGSS)
  • Mitosis, Meiosis and Fertilization Vocabulary Review Game
  • Genetics Concepts and Activities (NGSS)
  • Genetics (NGSS; hands-on)
  • Genetics Intro – Family Members (NGSS)
  • Genetics Sickle Cell Anemia and Trait (NGSS)
  • Genetics Probability – Sex Ratios (NGSS)
  • Mistake in copying DNA & Dwarfism (NGSS)
  • Soap Opera Genetics (NGSS)
  • Were the babies switched? The Genetics of Blood Types (NGSS; hands-on)
  • Dragon Genetics I (hands-on)
  • Dragon Genetics II (hands-on)
  • Learning about Genetic Disorders
  • Genetics Vocabulary Review Game
  • Genetics Jeopardy

Genealogy

Molecular Biology

  • Molecular Biology: Major Concepts and Learning Activities (NGSS)
  • DNA (NGSS; hands-on)
  • DNA Function, Structure and Replication (NGSS)
  • How Genes Can Cause Disease - Introduction to Transcription and Translation (NGSS; hands-on)
  • How Genes Can Cause Disease - Understanding Transcription and Translation (NGSS)
  • UV, Mutations and DNA Repair (NGSS; hands-on)
  • What types of mutations cause more vs. less severe muscular dystrophy? (NGSS)
  • Cell Differentiation and Epigenetics (NGSS)
  • Genetic Engineering Challenge – Preventing Vitamin A Deficiency (NGSS)
  • Gene Editing with CRISPR-Cas – Potential Sickle Cell Anemia Cure (NGSS)
  • Molecular Biology Vocabulary Review Game
  • Resources for Teaching and Learning about Evolution
  • Evolution by Natural Selection (NGSS; hands-on)
  • What is natural selection? (NGSS)
  • Natural Selection and the Peppered Moth (NGSS)
  • How have mutations and natural selection affected fur color in mice?  (NGSS)
  • How Whales Evolved (NGSS)
  • How Eyes Evolved – Analyzing the Evidence (NGSS)
  • How does evolution result in similarities and differences? (NGSS; hands-on)
  • What is a species? (NGSS)
  • Coronavirus Evolution and the COVID-19 Pandemic (NGSS)
  • Evolution and Adaptations (NGSS)
  • Ecology Concepts and Learning Activities (NGSS)
  • Exponential and Logistic Population Growth Models vs. Complex Reality (NGSS)
  • Some Similarities between the Spread of Infectious Disease and Population Growth  (NGSS; hands-on)
  • Stability and Change in Biological Communities (NGSS)
  • Food Webs, Energy Flow, Carbon Cycle and Trophic Pyramids (NGSS)
  • Food Webs (NGSS)
  • Carbon Cycles and Energy Flow through Ecosystems (NGSS)
  • Trophic Pyramids (NGSS)
  • Introduction to Global Warming (NGSS)
  • Food and Climate Change – How can we feed a growing world population without increasing global warming? (NGSS)
  • Resources for Teaching about Climate Change
  • The Ecology of Lyme Disease (NGSS)

Human Physiology and Health

  • Negative Feedback, Homeostasis, and Positive Feedback – Examples and Concepts  (NGSS; hands-on)
  • Homeostasis, Negative Feedback, and Positive Feedback  (NGSS)
  • How do we Sense the Flavors of Food?  (NGSS; hands-on)
  • COVID-19 Vaccines (NGSS)
  • How to Reduce the Spread of COVID-19  (NGSS)
  • Molecular and Evolutionary Biology of HIV/AIDS and Treatment (NGSS)
  • Resources for Teaching Cancer Biology
  • Carbohydrate Consumption, Athletics, Health – Using Science Process Skills
  • Vitamins and Health – Why Experts Disagree
  • Regulation of Human Heart Rate (hands-on)
  • Should You Drink Sports Drinks?  When?  Why?

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License . To preserve the value of these learning activities for other teachers, please do not post keys for any questions from any of these activities!

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Remote Ready Biology Learning Activities

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Remote Ready Biology Learning Activities  has 50 remote-ready activities, which work for either your classroom or remote teaching.

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Biology Worksheets, Notes, and Quizzes (PDF and PNG)

Biology Notes, Worksheets, and Quizzes

This is a collection of free biology worksheets, notes, handouts, slides, study guides and quizzes. Most content targets high school, AP biology, genetics, anatomy/physiology, immunology, and biology 101 and 102 in college. There is also biochemistry and physics for biologists. However, some resources are at the grade school and middle school level.

The files are PDF, PNG, JPG, and formats using Google Apps for Google Classroom. Most of the time, these formats are interchangeable. So, if you see something you like, but want a different format, just let us know. Print these resources, make transparencies and slides, etc.

In the interest of quick load time, not all of the images are shown. If you’d rather see them all, just contact us!

Biochemistry

Understanding the Differences Between RNA and DNA - Worksheet

[ Google apps worksheet ][ worksheet PDF ][ answers PDF ][ worksheet PNG ][ answers PNG ]

Enzymes Worksheet

Enzymes Definitions

[ Google Slides worksheet ][ worksheet PDF ][ answers PDF ][ worksheet PNG ][ answers PNG ]

  • 20 Amino Acids [ PNG ][ PDF ]
  • Amino Acid Side Chains [ PNG ][ PDF ]
  • Identifying Type of Biological Macromolecules [ Google Slides worksheet ][ worksheet PDF ][ answers PDF ][ worksheet PNG ][ answers PNG ]
  • Disaccharide Examples [ PNG ]
  • Products of Photosynthesis [ JPG ]
  • Anabolism vs Catabolism [ PNG ]
  • 3 Parts of a Nucleotide [ PNG ]
  • Fermentation Definition and Examples [ PNG ]

General and Cell Biology

Major Organelles and Their Function Worksheet

Organelles and Their Functions

Parts of a Plant Cell Worksheet

Parts of a Plant Cell

Anatomy of a Chloroplast Worksheet

Label Parts of a Chloroplast

[ Google Apps worksheet ][ worksheet PDF ][ answers PDF ][ worksheet PNG ][ answers PNG ]

Anatomy of the Mitochondria Worksheet

Label Parts of a Mitochondria

Animal Cell Worksheet

Label the Animal Cell

[ Google Apps worksheet ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]

Prokaryotes vs Eukaryotes Worksheet

Prokaryotes vs Eukaryotes Worksheet

Stages of the Cell Cycle Worksheet

Steps of the Cell Cycle

Stages of Mitosis Worksheet

Steps of Mitosis

Membrane Transport Worksheet

Membrane Transport Terms and Definitions

Membrane Transport Worksheet 2

Membrane Transport Worksheet #2

The Plasma Membrane Worksheet

The Plasma Membrane

Bacterial Cell Anatomy Worksheet

Label a Bacterial Cell

  • Label a Bacteriophage [ Google Apps worksheet ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]
  • Evidence of Evolution Worksheet [ Google Apps worksheet ][ Worksheet PDF ][ Worksheet PNG ][ Answers PNG ]
  • Evolutionary Processes Worksheet [ worksheet Google Apps ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]
  • Major Receptor Families [ Google Apps worksheet ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]
  • Label a Bacterial Cell Membrane ( E. coli ) [ Google Apps worksheet ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]

Anatomy and Physiology

These worksheets are only a portion of the available anatomy and physiology worksheets. Human anatomy and physiology worksheets have their own section.

Anatomy of the Heart Worksheet

Label the Heart

Anatomy of the Eye Worksheet

Label the Eye

[ Google Apps worksheet ][ worksheet PDF ][ answers PDF ][ worksheet PNG ]

Types of Blood Cells Worksheet

Types of Blood Cells

[ worksheet Google Apps ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]

The Main Anterior Muscles Worksheet

Label the Muscles

[ worksheet PDF ][ worksheet PNG ][ answers PNG ]

Anatomy of the ear worksheet

Label the Ear

[ Google Apps worksheet ][ Worksheet PDF ][ Worksheet PNG ][ Answers PNG ]

Anatomy of the Lungs Worksheet

Label the Lungs

Anatomy of a Kidney Worksheet

Label the Kidney

Anatomy of the Liver Worksheet

Label the Liver

Anatomy of the Large Intestine Worksheet

Label the Large Intestine

Anatomy of the Stomach Worksheet

Label the Stomach

[ Google Apps worksheet ] [Worksheet PDF ][ Worksheet PNG ][ Answers PNG ]

External Nose Anatomy Worksheet

External Nose Anatomy

[ Worksheet PDF ][ Worksheet Google Apps ][ Worksheet PNG ][ Answers PNG ]

Anatomy of the Nose Worksheet

Parts of the Nose

The Skeletal System Worksheet

Label Bones of the Skeleton

Anatomy of a Lymph Node - Worksheet

Label the Lymph Node

Anatomy of of the Brain Worksheet

Label the Parts of the Brain

Lobes of the Brain Worksheet

Label the Lobes of the Brain

Anatomical Directions of the Brain Worksheet

Brain Anatomical Sections

Arteries of the Brain Worksheet

Arteries of the Brain

Anatomy of the Pancreas Worksheet

Label the Pancreas

Anatomy of the Spleen Worksheet

Label the Spleen

The Digestive System Worksheet

Label the Digestive System

The Respiratory System Worksheet

Label the Respiratory System

Anatomy of a Neuron Worksheet

Parts of a Neuron

Lip Anatomy Worksheet

Label the Lips

Anatomy of the Skin Worksheet

Label the Skin

The Circulatory System Worksheet

Label the Circulatory System

The Excretory System Worksheet

The Urinary Tract

[ Worksheet PDF ][ Worksheet Google Apps ][ Worksheet PNG ][ Answer Key PNG ]

Anatomy of the Bladder Worksheet

The Bladder

  • The Female Reproductive System [ worksheet PDF ][ worksheet Google Apps ][ worksheet PNG ][ answers PNG ]

Parts of a Flower Worksheet

Parts of a Flower

Anatomy of an orchid Worksheet

Label the Orchid Plant

[ Worksheet PDF ][ Worksheet Google Apps ][ Worksheet PNG ] [Answer Key PNG ]

Parts of an orchid flower Worksheet

Parts of an Orchid Flower

Parts of a monocot seed Worksheet

Parts of a Monocot Seed

Parts of a fern Worksheet

Parts of a Fern

Parts of a tree trunk Worksheet

Parts of a Tree Trunk

Parts of a Tree Worksheet

Parts of a Tree

[ worksheet PDF ][ worksheet Google Apps ][ worksheet PNG ][ answers PNG ]

Basic Anatomy of a Mushroom Worksheet

Parts of a Mushroom

Parts of a Shark Worksheet

Label the Shark

Anatomy of a Fish Worksheet

Label the Fish

Parts of a Bird Worksheet

Parts of a Bird

Basic Anatomy of a Bird Worksheet

Bird Anatomy

Life Cycle of a Frog Worksheet

Frog Life Cycle

Basic Mosquito Anatomy Worksheet

Parts of a Mosquito (Insect)

biology classification assignment

Bones of the T. rex Skull

[ worksheets PDF ][ worksheet Google Slides ][ worksheet PNG ][ answers PNG ]

biology classification assignment

Holes of the T. rex Skull

  • Label the T. rex Skeleton [ worksheets PDF ][ worksheet Google Slides ][ worksheet PNG ][ answers PNG ]
  • Label Human Teeth [ Worksheet PDF ][ Worksheet Google Apps ][ Worksheet PNG ][ Answer Key PNG ]
  • Monocot vs Dicot Seeds [ worksheet PDF ][ worksheet Google Slides ][ worksheet PNG ][ answers PNG ]
  • Label the Moss [ worksheet PDF ][ worksheet Google Slides ][ worksheet PNG ][ answers PNG ]
  • Diagram of the Human Eye [ JPG ]

Use a completed worksheet as a study guide.

Cells of the Immune System Worksheet

Cells of the Immune System

Immune Cell Functions - Worksheet 1

Immune Cell Functions

[ worksheet Google Apps ][ worksheet PDF ][ worksheet PNG #1][ answers PNG #1][ worksheet PNG #2][ answers PNG #2]

Methods to Study Virus Structures Worksheet

Methods to Study Virus Structures

[ worksheet Google Slide ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]

Icosahedral Virus Capsids Worksheet

Icosahedral Virus Capsids

Human DNA Viruses Worksheet

Human DNA Viruses

Human RNA Viruses Worksheet

Human RNA Viruses

This is selection of worksheets relating to DNA, RNA, transcription, translation, genetic crosses, plasmid mapping, etc. See the full collection of genetics worksheets if you’re don’t see what you need.

DNA Replication Worksheet

DNA Replication

Types of Mutations Worksheet

Types of Mutations

Monohybrid Cross - Worksheet #1

Monohybrid Cross Worksheet #1

Monohybrid Cross - Worksheet #2

Monohybrid Cross Worksheet #2

Monohybrid Cross - Worksheet #3

Monohybrid Cross Worksheet #3

Monohybrid Cross 4 Multiple Alleles - Worksheet

Monohybrid Cross #4 – Multiple Alleles

  • Monohybrid Cross Worksheet #5: Multiple Alleles [ worksheet Google Apps ][ worksheet PDF ][ worksheet PNG ][ answers PNG ]

Monohybrid Cross 6 Sex-Linked Inheritance Worksheet

Monohybrid Cross #6 – Sex-Linked Inheritance

Sex-Linked Inheritance Worksheet

Monohybrid Cross #7 – Sex-Linked Inheritance

Dihybrid Cross - Worksheet #1

Dihybrid Cross Worksheet #1

Dihybrid Cross 2 - Worksheet (8.5 × 11 in)

Dihybrid Cross Worksheet #2

Dihybrid Cross 3 - Student (8.5 × 11 in)

Dihybrid Cross Worksheet #3

Dihybrid Cross 4 - Student (8.5 × 11 in)

Dihybrid Cross Worksheet #4

Dihybrid Cross 5 Epistasis Worksheet

Dihybrid Cross #5 – Epistasis

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biology classification assignment

Cells are the basic, fundamental unit of life. So, if we were to break apart an organism to the cellular level, the smallest independent component that we would find would be the cell.

Explore the cell notes to know what is a cell, cell definition, cell structure, types and functions of cells. These notes have an in-depth description of all the concepts related to cells.

Table of Contents

Cell Definition

What is a cell, characteristics of cells, types of cells, cell structure, cell theory.

  • Functions of a Cell

Cells

Cells are the fundamental unit of life. They range in size from 0.0001 mm to nearly 150 mm across.

“A cell is defined as the smallest, basic unit of life that is responsible for all of life’s processes.”

Cells are the structural, functional, and biological units of all living beings. A cell can replicate itself independently. Hence, they are known as the building blocks of life . 

Each cell contains a fluid called the cytoplasm, which is enclosed by a membrane. Also present in the cytoplasm are several biomolecules like proteins, nucleic acids and lipids. Moreover, cellular structures called cell organelles are suspended in the cytoplasm.

A cell is the structural and fundamental unit of life. The study of cells from its basic structure to the functions of every cell organelle is called Cell Biology. Robert Hooke was the first Biologist who discovered cells.

All organisms are made up of cells. They may be made up of a single cell (unicellular), or many cells (multicellular).  Mycoplasmas are the smallest known cells. Cells are the building blocks of all living beings. They provide structure to the body and convert the nutrients taken from the food into energy.

Cells are complex and their components perform various functions in an organism. They are of different shapes and sizes, pretty much like bricks of the buildings. Our body is made up of cells of different shapes and sizes.

Cells are the lowest level of organisation in every life form. From organism to organism, the count of cells may vary. Humans have more number of cells compared to that of  bacteria .

Cells comprise several cell organelles that perform specialised functions to carry out life processes. Every organelle has a specific structure. The hereditary material of the organisms is also present in the cells.

Discovery of Cells

Discovery of cells is one of the remarkable advancements in the field of science. It helps us know that all the organisms are made up of cells, and these cells help in carrying out various life processes. The structure and functions of cells helped us to understand life in a better way.

Who discovered cells?

Robert Hooke discovered the cell in 1665. Robert Hooke observed a piece of bottle cork under a compound microscope and noticed minuscule structures that reminded him of small rooms. Consequently, he named these “rooms” as cells. However, his compound microscope had limited magnification, and hence, he could not see any details in the structure. Owing to this limitation, Hooke concluded that these were non-living entities.

Later Anton Van Leeuwenhoek observed cells under another compound microscope with higher magnification. This time, he had noted that the cells exhibited some form of movement (motility). As a result, Leeuwenhoek concluded that these microscopic entities were “alive.” Eventually, after a host of other observations, these entities were named as animalcules.

In 1883, Robert Brown, a Scottish botanist, provided the very first insights into the cell structure. He was able to describe the nucleus present in the cells of orchids.

Following are the various essential characteristics of cells:

  • Cells provide structure and support to the body of an organism.
  • The cell interior is organised into different individual organelles surrounded by a separate membrane.
  • The nucleus (major organelle) holds genetic information necessary for reproduction and cell growth.
  • Every cell has one nucleus and membrane-bound organelles in the cytoplasm.
  • Mitochondria, a double membrane-bound organelle is mainly responsible for the energy transactions vital for the survival of the cell.
  • Lysosomes digest unwanted materials in the cell.
  • Endoplasmic reticulum plays a significant role in the internal organisation of the cell by synthesising selective molecules and processing, directing and sorting them to their appropriate locations.

Also Read : Nucleus

Cells are similar to factories with different labourers and departments that work towards a common objective. Various types of cells perform different functions. Based on cellular structure, there are two types of cells:

  • Prokaryotes

Explore:   Difference Between Prokaryotic and Eukaryotic Cells

Prokaryotic Cells

Main article: Prokaryotic Cells

  • Prokaryotic cells have no nucleus. Instead, some prokaryotes such as bacteria have a region within the cell where the genetic material is freely suspended. This region is called the nucleoid.
  • They all are single-celled microorganisms. Examples include archaea, bacteria, and cyanobacteria.
  • The cell size ranges from 0.1 to 0.5 µm in diameter.
  • The hereditary material can either be DNA or RNA.
  • Prokaryotes generally reproduce by binary fission, a form of asexual reproduction. They are also known to use conjugation – which is often seen as the prokaryotic equivalent to sexual reproduction (however, it is NOT sexual reproduction).

Eukaryotic Cells

Main article : Eukaryotic Cells

  • Eukaryotic cells are characterised by a true nucleus.
  • The size of the cells ranges between 10–100 µm in diameter.
  • This broad category involves plants, fungi, protozoans, and animals.
  • The plasma membrane is responsible for monitoring the transport of nutrients and electrolytes in and out of the cells. It is also responsible for cell to cell communication.
  • They reproduce sexually as well as asexually.
  • There are some contrasting features between plant and animal cells. For eg., the plant cell contains chloroplast, central vacuoles, and other plastids, whereas the animal cells do not.

The cell structure comprises individual components with specific functions essential to carry out life’s processes. These components include- cell wall, cell membrane, cytoplasm, nucleus, and cell organelles. Read on to explore more insights on cell structure and function.

Cell Membrane

  • The cell membrane supports and protects the cell. It controls the movement of substances in and out of the cells. It separates the cell from the external environment. The cell membrane is present in all the cells.
  • The cell membrane is the outer covering of a cell within which all other organelles, such as the cytoplasm and nucleus, are enclosed. It is also referred to as the plasma membrane.
  • By structure, it is a porous membrane (with pores) which permits the movement of selective substances in and out of the cell.  Besides this, the cell membrane also protects the cellular component from damage and leakage.
  • It forms the wall-like structure between two cells as well as between the cell and its surroundings.
  • Plants are immobile, so their cell structures are well-adapted to protect them from external factors. The cell wall helps to reinforce this function.
  • The cell wall is the most prominent part of the plant’s cell structure. It is made up of cellulose, hemicellulose and pectin.
  • The cell wall is present exclusively in plant cells. It protects the plasma membrane and other cellular components. The cell wall is also the outermost layer of plant cells.
  • It is a rigid and stiff structure surrounding the cell membrane.
  • It provides shape and support to the cells and protects them from mechanical shocks and injuries.
  • The cytoplasm is a thick, clear, jelly-like substance present inside the cell membrane.
  • Most of the chemical reactions within a cell take place in this cytoplasm.
  • The cell organelles such as endoplasmic reticulum, vacuoles, mitochondria, ribosomes, are suspended in this cytoplasm.
  • The nucleus contains the hereditary material of the cell, the DNA.
  • It sends signals to the cells to grow, mature, divide and die.
  • The nucleus is surrounded by the nuclear envelope that separates the DNA from the rest of the cell.
  • The nucleus protects the DNA  and is an integral component of a plant’s cell structure.

Cell Organelles

Cells are composed of various cell organelles that perform certain specific functions to carry out life’s processes. The different cell organelles, along with its principal functions, are as follows:

Cell Theory was proposed by the German scientists,  Theodor Schwann, Matthias Schleiden, and Rudolf Virchow. The cell theory states that:

  • All living species on Earth are composed of cells.
  • A cell is the basic unit of life.
  • All cells arise from pre-existing cells.

A modern version of the cell theory was eventually formulated, and it contains the following postulates:

  • Energy flows within the cells.
  • Genetic information is passed on from one cell to the other.
  • The chemical composition of all the cells is the same.

Functions of Cell

A cell performs major functions essential for the growth and development of an organism. Important functions of cell are as follows:

Provides Support and Structure

All the organisms are made up of cells. They form the structural basis of all the organisms. The cell wall and the cell membrane are the main components that function to provide support and structure to the organism. For eg., the skin is made up of a large number of cells. Xylem present in the vascular plants is made of cells that provide structural support to the plants.

Facilitate Growth Mitosis

In the process of mitosis, the parent cell divides into the daughter cells. Thus, the cells multiply and facilitate the growth in an organism.

Allows Transport of Substances

Various nutrients are imported by the cells to carry out various chemical processes going on inside the cells. The waste produced by the chemical processes is eliminated from the cells by active and passive transport. Small molecules such as oxygen, carbon dioxide, and ethanol diffuse across the cell membrane along the concentration gradient. This is known as passive transport. The larger molecules diffuse across the cell membrane through active transport where the cells require a lot of energy to transport the substances.

Energy Production

Cells require energy to carry out various chemical processes. This energy is produced by the cells through a process called   photosynthesis in plants and respiration in animals.

Aids in Reproduction

A cell aids in reproduction through the processes called mitosis and meiosis. Mitosis is termed as the asexual reproduction where the parent cell divides to form daughter cells. Meiosis causes the daughter cells to be genetically different from the parent cells.

Thus, we can understand why cells are known as the structural and functional unit of life. This is because they are responsible for providing structure to the organisms and perform several functions necessary for carrying out life’s processes.

Also Read:  Difference Between Plant Cell and Animal Cell

To know more about what is a cell, its definition, cell structure, types of cells, the discovery of cells, functions of cells or any other related topics, explore  BYJU’S Biology . Alternatively, download BYJU’S app for a personalised learning experience.

biology classification assignment

Frequently Asked Questions

1. what is a cell, 2. state the characteristics of cells..

  • Cells provide the necessary structural support to an organism.
  • The genetic information necessary for reproduction is present within the nucleus.
  • Structurally, the cell has cell organelles which are suspended in the cytoplasm.
  • Mitochondria is the organelle responsible for fulfilling the cell’s energy requirements.
  • Lysosomes digest metabolic wastes and foreign particles in the cell.
  • Endoplasmic reticulum synthesises selective molecules and processes them, eventually directing them to their appropriate locations.

3. Highlight the cell structure and its components.

The cell structure comprises several individual components which perform specific functions essential to carry out life processes. The components of the cell are as follows:

  • Cell membrane
  • Nuclear membrane
  • Endoplasmic reticulum
  • Golgi Bodies
  • Mitochondria
  • Chloroplast

4. State the types of cells.

Cells are primarily classified into two types, namely

  • Prokaryotic cells
  • Eukaryotic cells

5. Elaborate Cell Theory.

Cell Theory was proposed by  Matthias Schleiden, Theodor Schwann, and Rudolf Virchow, who were German scientists. The cell theory states that:

6. What is the function of mitochondria in the cells?

7. what are the functions of the cell.

The essential functions of the cell include:

  • The cell provides support and structure to the body.
  • It facilitates growth by mitosis.
  • It helps in reproduction.
  • Provides energy and allows the transport of substances.

8. What is the function of Golgi bodies?

9. who discovered the cell and how, 10. name the cell organelle that contains hydrolytic enzymes capable of breaking down organic matter., 11. which cellular structure regulates the entry and exit of molecules to and from the cell.

Register at BYJU’S for cell related Biology notes. Refer to these notes for reference.

Further Reading:  Cell Biology MCQs

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  • Short Report
  • Open access
  • Published: 13 May 2024

Commonly used software tools produce conflicting and overly-optimistic AUPRC values

  • Wenyu Chen 1   na1 ,
  • Chen Miao 1   na1 ,
  • Zhenghao Zhang 2 ,
  • Cathy Sin-Hang Fung 1 ,
  • Ran Wang 1 ,
  • Yizhen Chen 2 ,
  • Yan Qian 3 ,
  • Lixin Cheng 4 ,
  • Kevin Y. Yip 2 , 5 ,
  • Stephen Kwok-Wing Tsui 1 , 6 &
  • Qin Cao   ORCID: orcid.org/0000-0002-3106-562X 1 , 6 , 7  

Genome Biology volume  25 , Article number:  118 ( 2024 ) Cite this article

197 Accesses

4 Altmetric

Metrics details

The precision-recall curve (PRC) and the area under the precision-recall curve (AUPRC) are useful for quantifying classification performance. They are commonly used in situations with imbalanced classes, such as cancer diagnosis and cell type annotation. We evaluate 10 popular tools for plotting PRC and computing AUPRC, which were collectively used in more than 3000 published studies. We find the AUPRC values computed by the tools rank classifiers differently and some tools produce overly-optimistic results.

Introduction

Many problems in computational biology can be formulated as binary classification, in which the goal is to infer whether an entity (e.g., a cell) belongs to a target class (e.g., a cell type). Accuracy, precision, sensitivity (i.e., recall), specificity, and F1 score (Additional file 1 : Fig. S1) are some of the measures commonly used to quantify classification performance, but they all require a threshold of the classification score to assign every entity to either the target class or not. The receiver operating characteristic (ROC) and precision-recall curve (PRC) avoid this problem by considering multiple thresholds [ 1 ], which allows detailed examination of the trade-off between identifying entities of the target class and wrongly including entities not of this class. It is common to summarize these curves by the area under them (AUROC and AUPRC, respectively), which is a value between 0 and 1, with a larger value corresponding to better classification performance.

When the different classes have imbalanced sizes (e.g., the target cell type has few cells), AUPRC is a more sensitive measure than AUROC [ 1 , 2 , 3 , 4 ], especially when there are errors among the top predictions (Additional file 1 : Fig. S2). As a result, AUPRC has been used in a variety of applications, such as reconstructing biological networks [ 5 ], identifying cancer genes [ 6 ] and essential genes [ 7 ], determining protein binding sites [ 8 ], imputing sparse experimental data [ 9 ], and predicting patient treatment response [ 10 ]. AUPRC has also been extensively used as a performance measure in benchmarking studies, such as the ones for comparing methods for analyzing differential gene expression [ 11 ], identifying gene regulatory interactions [ 12 ], and inferring cell-cell communications [ 13 ] from single-cell RNA sequencing data.

Given the importance of PRC and AUPRC, we analyzed commonly used software tools and found that they produce contrasting results, some of which are overly-optimistic.

For each entity, a classifier outputs a score to indicate how likely it belongs to the target (i.e., “positive”) class. Depending on the classifier, the score can be discrete (e.g., random forest) or continuous (e.g., artificial neural network). Using a threshold t , the classification scores can be turned into binary predictions by considering all entities with a score \(\ge t\) as belonging to the positive class and all other entities as not. When these predictions are compared to the actual classes of the entities, precision is defined as the proportion of entities predicted to be positive that are actually positive, while recall is defined as the proportion of actually positive entities that are predicted to be positive (Additional file 1 : Fig. S1).

The PRC is a curve that shows how precision changes with recall. In the most common way to produce the PRC, each unique classification score observed is used as a threshold to compute a pair of precision and recall values, which forms an anchor point on the PRC. Adjacent anchor points are then connected to produce the PRC.

When no two entities have the same score (Fig.  1 a), it is common to connect adjacent anchor points directly by a straight line [ 14 , 15 , 16 , 17 , 18 , 19 ] (Fig.  1 b). Another method uses an expectation formula, which we will explain below, to connect discrete points by piece-wise linear lines [ 20 ] (Fig.  1 c). The third method is to use the same expectation formula to produce a continuous curve between adjacent anchor points [ 17 , 21 ] (Fig.  1 d). A fourth method that has gained popularity, known as Average Precision (AP), connects adjacent anchor points by step curves [ 15 , 19 , 22 , 23 ] (Fig.  1 e). In all four cases, PRC estimates a function of precision in terms of recall based on the observed classification scores of the entities, and AUPRC estimates the integral of this function using trapezoids (in the direct straight line case), interpolation lines/curves (in the expectation cases), or rectangles (in the AP case).

figure 1

Different methods for connecting adjacent anchor points on the PRC. a An illustrative data set with no two entities receiving the same classification score. b – e Different methods for connecting adjacent anchor points when there are no ties in classification scores, namely b direct straight line, c discrete expectation, d continuous expectation, and e AP. f An illustrative data set with different entities receiving the same classification score. Each group of entities with the same classification score defines a single anchor point (A, B, C, and D, from 3, 7, 2, and 1 entities, respectively). g – j Different methods for connecting anchor point B to its previous anchor point, A, namely g linear interpolation, h discrete expectation, i continuous expectation, and j AP. In c and h , tp is set to 0.5 and 1 in Formula 1, respectively (Additional file 1 : Supplementary Text)

When there are ties with multiple entities having the same score, which happens more easily with classifiers that produce discrete scores, these entities together define only one anchor point (Fig.  1 f). There are again four common methods for connecting such an anchor point to the previous anchor point, which correspond to the four methods for connecting anchor points when there are no ties (details in Additional file 1 : Supplementary Text). The first method is to connect the two anchor points by a straight line [ 15 , 18 , 19 ] (Fig.  1 g). This method is known to easily produce overly-optimistic AUPRC values [ 2 , 24 ], which we will explain below. The second method is to interpolate additional points between the two anchor points using a non-linear function and then connect the points by straight lines [ 14 , 17 , 20 ] (Fig.  1 h). The interpolated points appear at their expected coordinates under the assumption that all possible orders of the entities with the same score have equal probability. The third method uses the same interpolation formula as the second method but instead of creating a finite number of interpolated points, it connects the two anchor points by a continuous curve [ 17 , 21 ] (Fig.  1 i). Finally, the fourth method comes naturally from the AP approach, which uses step curves to connect the anchor points [ 15 , 19 , 22 , 23 ] (Fig.  1 j).

Using the four methods to connect anchor points when there are no ties and the four methods when there are ties can lead to very different AUPRC values (Fig.  1 , Additional file 1 : Fig. S3 and Supplementary Text).

Conceptual and implementation issues of some popular software tools

We analyzed 10 tools commonly used to produce PRC and AUPRC (Additional file 1 : Table S1). Based on citations and keywords, we estimated that these tools have been used in more than 3000 published studies in total ( Methods ).

The 10 tools use different methods to connect anchor points on the PRC and therefore they can produce different AUPRC values (Table  1 , Additional file 1 : Fig. S4–S7 and Supplementary Text). As a comparison, all 10 tools can also compute AUROC, and we found most of them to produce identical values (Additional file 1 : Supplementary Text).

We found five conceptual issues with some of these tools when computing AUPRC values (Table  1 ):

➀ Using the linear interpolation method to handle ties, which can produce overly-optimistic AUPRC values [ 2 , 24 ]. When interpolating between two anchor points, linear interpolation produces higher AUPRC than the other three methods under conditions that can easily happen in real situations (Additional file 1 : Supplementary Text)

➁ Always using (0, 1) as the starting point of the PRC (procedurally produced or conceptually derived, same for ➂ and ➄ below), which is inconsistent with the concepts behind the AP and non-linear expectation methods when the first anchor point with a non-zero recall does not have a precision of one (Additional file 1 : Supplementary Text)

➂ Not producing a complete PRC that covers the full range of recall values from zero to one

➃ Ordering entities with the same classification score by their order in the input and then handling them as if they have distinct classification scores

➄ Not putting all anchor points on the PRC

These issues can lead to overly-optimistic AUPRC values or change the order of two AUPRC values (Additional file 1 : Supplementary Text and Fig. S8-S13).

Some of these tools also produce a visualization of the PRC. We found three types of issues with these visualizations (Table  1 ):

Producing a visualization of PRC that has the same issue(s) as in the calculation of AUPRC

Producing a PRC visualization that does not always start the curve at a point with zero recall

Producing a PRC visualization that always starts at (0, 1)

biology classification assignment

Inconsistent AUPRC values and contrasting classifier ranks produced by the popular tools

To see how the use of different methods by the 10 tools and their other issues affect PRC analysis in practice, we applied them to evaluate classifiers in four realistic scenarios.

In the first scenario, we analyzed data from a COVID-19 study [ 25 ] in which patient blood samples were subjected to Cellular Indexing of Transcriptomes and Epitopes by Sequencing (CITE-seq) assays [ 26 ]. We constructed a classifier for predicting CD4 \(^+\) T cells, which groups the cells based on their transcriptome data alone and assigns a single cell type label to each group. Using cell type labels defined by the original authors as reference, which were obtained using both antibody-derived tags (ADTs) and transcriptome data, we computed the AUPRC of the classifier. Figure  2 a shows that the 10 tools produced 6 different AUPRC values, ranging from 0.416 to 0.684. In line with the conceptual discussions above, the AP method generally produced the smallest AUPRC values while the linear interpolation method generally produced the largest, although individual issues of the tools created additional variations of the AUPRC values computed.

figure 2

The AUPRC values computed by the 10 tools in several realistic scenarios. a Predicting CD4 \(^+\) T cells from single-cell transcriptomic data. b Predicting inflammatory bowel disease cases that belong to the ulcerative colitis subtype in the sbv IMPROVER Metagenomics Diagnosis for Inflammatory Bowel Disease Challenge. Only the top 8 submissions according to PRROC (discrete expectation) AUPRC values are included. c Predicting cases with preterm prelabor rupture of membranes in the DREAM Preterm Birth Prediction Challenge. In b and c , each entry shows the AUPRC value and the background color indicates its rank among the competitors

In the second scenario, we compared the performance of different classifiers that predict whether a patient has the ulcerative colitis (UC) subtype of inflammatory bowel disease (IBD) or does not have IBD, based on metagenomic data (processed taxonomy-based profile) [ 27 ]. The predictions made by these classifiers were submitted to the sbv IMPROVER Metagenomics Diagnosis for IBD Challenge. Their performance was determined by comparing against diagnosis of these patients based on clinical, endoscopic, and histological criteria. Figure  2 b shows that based on the AUPRC values computed, the 10 tools ranked the classifiers differently. For example, among the top 8 submissions with the highest performance, the classifier in submission 26 was ranked first in 8 cases, sole second place in 2 cases, and tied second place with another classifier in 4 cases (Fig.  2 b and Additional file 1 : Fig. S14). We observed similar rank flips when considering the top 30 submissions (Additional file 1 : Fig. S15 and S16).

In the third scenario, we compared the performance of different classifiers in identifying preterm prelabor rupture of the membranes (PPROM) cases from normal pregnancy in the DREAM Preterm Birth Prediction Challenge [ 28 ]. Based on the AUPRC values produced by the 10 tools, the 13 participating teams were ranked very differently (Fig.  2 c and Additional file 1 : Fig. S17). For example, Team “GZCDC” was ranked first (i.e., highest) in 3 cases, tenth in 4 cases, and thirteenth (i.e., lowest) in 7 cases. In addition to differences in the ranks, some of the AUPRC values themselves are also very different. For example, the AUPRC values computed by PerfMeas and MLeval have a Pearson correlation of − 0.759.

In the fourth scenario, we compared 29 classifiers that predicted target genes of transcription factors in the DREAM5 challenge [ 29 ]. Again, some classifiers received very different ranking based on the AUPRC values computed by the different tools (Additional file 1 : Fig. S18 and S19). For example, the classifier named “Other4” was ranked second based on the AUPRC values computed by PerfMeas but it was ranked twenty-fifth based on the AUPRC values computed by MLeval. In general, tools that use the discrete expectation, continuous expectation, and AP methods are in good agreements in this scenario, but they differ substantially from tools that use the linear interpolation method.

Conclusions

Due to their highly technical nature, it is easy to overlook the inconsistencies and issues of the software tools used for producing PRC and AUPRC. Some possible consequences include reporting overly-optimistic AUPRC, ranking classifiers differently by different tools, and introducing biases to the evaluation process, such as inflating the AUPRC of classifiers that produce discrete scores.

To address the problems, it is crucial to use tools that are free of the bugs described and avoid using the linear interpolation method (Table  1 ). It is also necessary to state clearly in manuscripts both the tool used (with its version number) and the underlying methods implemented by the tool for producing PRC and AUPRC. Whenever feasible, the adoption of multiple tools that implement different methods (e.g., one based on continuous expectation and one based on AP) is recommended, with comprehensive reporting of all their results.

Information about the tools

In this study, we included 12 tools commonly used for PRC and ROC analyses (Additional file 1 : Table S1). For each tool, we analyzed the latest stable version of it as of August 15, 2023. Because TorchEval had not released a stable version, we analyzed the latest version of it, version 0.0.6. Among the 12 tools, ten can compute both AUROC and AUPRC, while the remaining two can only compute AUROC. We focused on these 10 tools in the study of PRC and AUPRC. Some tools provide multiple methods for computing AUROC/AUPRC.

For tools with an associated publication, we obtained its citation count from Google Scholar. If a tool has multiple associated publications, we selected the one with the largest number of citations. As a result, the citation counts we report in Additional file 1 : Table S1 are underestimates if different publications associated with the same tool are not always cited together.

The Comprehensive R Archive Network (CRAN) packages PerfMeas and MLeval did not have an associated formal publication but only release notes. In each of these cases, we used the package name as keyword to search on Google Scholar and then manually checked the publications returned to determine the number of publications that cited these packages.

The CRAN package yardstick also did not have an associated formal publication. However, we were not able to use the same strategy as PerMeas and MLeval to determine the number of publications that cited the yardstick package since “yardstick” is an English word and the search returned too many publications to be verified manually. Therefore, we only counted the number of publications that cited yardstick’s release note, which is likely an underestimate of the number of publications that cited yardstick.

All citation counts were collected on October 9, 2023.

For tools with an associated formal publication, based on our collected lists of publications citing the tools, we further estimated the number of times the tools were actually used in the studies by performing keyword-based filtering. Specifically, if the main text or figure captions of a publication contains either one of the keywords “AUC” and “AUROC,” we assumed that the tool was used in that published study to perform ROC analysis. In the case of PRC, we performed filtering in two different ways and reported both sets of results in Additional file 1 : Table S1. In the first way, we assumed a tool was used in a published study if the main text or figure captions of the publication contains any one of the following keywords: “AUPR,” “AU-PR,” “AUPRC,” “AU-PRC,” “AUCPR,” “AUC-PR,” “PRAUC,” “PR-AUC,” “area under the precision recall,” and “area under precision recall.” In the second way, we assumed a tool was used in a published study if the main text or figure captions of the publication contains both “area under” and “precision recall.”

For the CRAN packages PerfMeas and MLeval, we estimated the number of published studies that actually used them by searching Google Scholar using the above three keyword sets each with the package name appended. We found that for all the publications we considered as using the packages in this way, they were also on our lists of publications that cite these packages. We used the same strategy to identify published studies that used the CRAN package yardstick. We found that some of these publications were not on our original list of publications that cite yardstick, and therefore we added them to the list and updated the citation count accordingly.

TorchEval was officially embedded into PyTorch in 2022. Due to its short history, among the publications that cite the PyTorch publication, we could not find any of them that used the TorchEval library.

Data collection and processing

We used four realistic scenarios to illustrate the issues of the AUPRC calculations.

In the first scenario, we downloaded CITE-seq data produced from COVID-19 patient blood samples by the COVID-19 Multi-Omic Blood ATlas (COMBAT) consortium [ 25 ]. We downloaded the data from Zenodo [ 30 ] and used the data in the “COMBAT-CITESeq-DATA” archive in this study. We then used a standard procedure to cluster the cells based on the transcriptome data and identified CD4 \(^+\) T cells. Specifically, we extracted the raw count matrix of the transcriptome data and ADT features (“X” object) and the annotation data frame (“obs” object) from the H5AD file. We dropped all ADT features (features with names starting with “AB-”) and put the transcriptome data along with the annotation data frame into Seurat (version 4.1.1). We then log-normalized the transcriptome data (method “NormalizeData(),” default parameters), identified highly-variable genes (method “FindVariableFeatures(),” number of variable genes set to 10,000), scaled the data (method “ScaleData(),” default parameters), performed principal component analysis (method “RunPCA(),” number of principal components set to 50), constructed the shared/k-nearest neighbor (SNN/kNN) graph (method “FindNeighbours(),” default parameters), and performed Louvain clustering of the cells (method “FindClusters(),” default parameters). We then extracted the clustering labels generated and concatenated them with cell type, major subtype, and minor subtype annotations provided by the original authors, which were manually curated using both ADT and transcriptome information.

Our procedure produced 29 clusters, which contained 836,148 cells in total. To mimic a classifier that predicts CD4 \(^+\) T cells using the transcriptome data alone, we selected one cluster and “predicted” all cells in it as CD4 \(^+\) T cells and all cells in the other 28 clusters as not, based on which we computed an AUPRC value by comparing these “predictions” with the original authors’ annotations. We repeated this process for each of the 29 clusters in turn, and chose the one that gave the highest AUPRC as the final cluster of predicted CD4 \(^+\) T cells.

For the second scenario, we obtained the data set used in the sbv IMPROVER (Systems Biology Verification combined with Industrial Methodology for PROcess VErification in Research) challenge on inflammatory bowel disease diagnosis based on metagenomics data [ 27 ]. The challenge involved 12 different tasks, and we focused on the task of identifying UC samples from non-IBD samples using the processed taxonomy-based profile as features. The data set contained 32 UC samples and 42 non-IBD samples, and therefore the baseline AUPRC was \(\frac{32}{32+42} = 0.432\) . There were 60 submissions in total, which used a variety of classifiers. We obtained the classification scores in the submissions from Supplementary Information 4 of the original publication [ 27 ]. When we extracted the classification scores of each submission, we put the actual positive entities before the actual negative entities. This ordering did not affect the AUPRC calculations of most tools except those of PerfMeas, which depend on the input order of the entities with the same classification score.

To see how the different tools rank the top submissions, we first computed the AUPRC of each submission using PRROC (option that uses the discrete expectation method to handle ties) since we did not find any issues with its AUPRC calculations (Table  1 ). We then analyzed the AUPRC values produced by the 10 tools based on either the top 8 (Fig.  2 b and Additional file 1 : Fig. S14) or top 30 (Additional file 1 : Fig. S15 and S16) submissions.

For the third scenario, we downloaded the data set used in the Dialogue on Reverse Engineering Assessment and Methods (DREAM) Preterm Birth Prediction Challenge [ 28 ] from https://www.synapse.org/#!Synapse:syn22127152 . We collected the classification scores, from the object “prpile” in each team’s RData file, and the actual classes produced based on clinical evidence, from “anoSC2_v21_withkey.RData” ( https://www.synapse.org/#!Synapse:syn22127343 ). The challenge contained 7 scenarios, each of which had 2 binary classification tasks. For each scenario, 10 different partitioning of the data into training and testing sets were provided. We focused on the task of identifying PPROM cases from the controls under the D2 scenario defined by the challenge. For this task, the baseline AUPRC value averaged across the 10 testing sets was 0.386. There were 13 participating teams in total. For each team, we extracted its classification scores and placed the actual positive entities before the actual negative entities. For submissions that contained negative classification scores, we re-scaled all the scores to the range between 0 and 1 without changing their order since TensorFlow expects all classification scores to be between zero and one (Additional file 1 : Supplementary Text). Finally, for each team, we computed its AUPRC using each of the 10 testing sets and reported their average. We note that the results we obtained by using PRROC (option that uses the continuous expectation method to handle ties) were identical to those reported by the challenge organizer.

For the fourth scenario, we obtained the data set used in the DREAM5 challenge on reconstructing transcription factor-target networks based on gene expression data [ 29 ]. The challenge included multiple networks and we focused on the E. coli in silico Network 1, which has a structure that corresponds to the real E. coli transcriptional regulatory network [ 29 ]. We obtained the data from Supplementary Data of the original publication [ 29 ]. There were 29 submissions in total. For each submission, we extracted the classification scores of the predicted node pairs (each pair involves one potential transcription factor and one gene it potentially regulates) from Supplementary Data 3 and compared them with the actual classes (positive if the transcription factor actually regulates the gene; negative if not) in the gold-standard network from Supplementary Data 1. Both the submissions and the gold-standard were not required to include all node pairs. To handle this, we excluded all node pairs in a submission that were not included in the gold-standard (because we could not judge whether they are actual positives or actual negatives), and assigned a classification score of 0 to all node pairs in the gold-standard that were not included in a submission (because the submission did not give a classification score to them). The gold-standard contained 4012 interacting node pairs and 274,380 non-interacting node pairs, and therefore the baseline AUPRC value was \(\frac{4012}{4012+274380} = 0.014\) .

Availability of data and materials

Our code is written in Java, Python and R. The reproducible code and all the data used in this paper are available at GitHub [ 31 ] and Zenodo [ 32 ].

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Review history

The review history is available as Additional file 2 .

Peer review information

Andrew Cosgrove was the primary editor of this article and managed its editorial process and peer review in collaboration with the rest of the editorial team.

QC is supported by National Natural Science Foundation of China under Award Number 32100515. YQ is supported by Guangdong Basic and Applied Basic Research Foundation under Award Number 2021A1515110759 and Natural Science Foundation of Guangdong Province of China under Award Number 2023A1515011187. LC is supported by National Natural Science Foundation of China under Award Number 32370711 and Shenzhen Medical Research Fund under Award Number A2303033. KYY is supported by National Cancer Institute of the National Institutes of Health under Award Number P30CA030199, National Institute on Aging of the National Institutes of Health under Award Numbers U54AG079758 and R01AG085498, and internal grants of Sanford Burnham Prebys Medical Discovery Institute. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

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Wenyu Chen and Chen Miao are co-first authors.

Authors and Affiliations

School of Biomedical Sciences, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China

Wenyu Chen, Chen Miao, Cathy Sin-Hang Fung, Ran Wang, Stephen Kwok-Wing Tsui & Qin Cao

Department of Computer Science and Engineering, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China

Zhenghao Zhang, Yizhen Chen & Kevin Y. Yip

The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China

Shenzhen People’s Hospital, First Affiliated Hospital of Southern University of Science and Technology, Second Clinical Medical College of Jinan University, Shenzhen, China

Lixin Cheng

Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA

Kevin Y. Yip

Hong Kong Bioinformatics Centre, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China

Stephen Kwok-Wing Tsui & Qin Cao

Shenzhen Research Institute, The Chinese University of Hong Kong, Shenzhen, China

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KYY, SKWT, and QC conceived and supervised the project. WC, CM, KYY, and QC designed the computational experiments and data analyses. WC, CM, and YC surveyed and collected the tools. WC, CM, ZZ, CSHF, and RW prepared the data. WC and CM conducted the computational experiments. WC, CM, ZZ, and RW performed the data analyses. All the authors interpreted the results. WC, CM, KYY, and QC wrote the manuscript.

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Correspondence to Kevin Y. Yip , Stephen Kwok-Wing Tsui or Qin Cao .

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Chen, W., Miao, C., Zhang, Z. et al. Commonly used software tools produce conflicting and overly-optimistic AUPRC values. Genome Biol 25 , 118 (2024). https://doi.org/10.1186/s13059-024-03266-y

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ECON 3130: Statistics and Probability. I had Professor Doug McKee for four consecutive semesters at Cornell, but this class was by far one of my favorites because of the time we took to understand the nuances and logic behind probability. I think economics and chemistry rely heavily on statistical theory to explain how their fields work because we can’t “see” every single molecule in a reaction or every single individual in a population. This class taught me to appreciate the math behind how we treat information that is too vast to understand and made me a better student of chemistry and economics because of it.

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Being brave in uncertain situations. I think a lot of Cornell students come from strong academic backgrounds where there is always a surefire way of achieving success. The real world is not so straightforward and sometimes you have to be willing to invest time and energy into a project, extracurricular or activity not knowing whether or not it will be successful. I think the second part of this skill is accepting unexpected/undesired outcomes and having the self-confidence to learn and move forward. There is no such thing as a failed experiment if you can learn something from the results.    

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When Hanjun Lee arrived at MIT, he was set on becoming a Course 5 chemistry student. Based on his experience in high school, biology was all about rote memorization.

That changed when he took course  7.03 (Genetics) , taught by then-professor  Aviv Regev , now head and executive vice president of research and early development at Genentech, and  Peter Reddien , professor of biology and core member and associate director of the Whitehead Institute for Biomedical Research.

He notes that friends from other schools don’t cite a single course that changed their major, but he’s not alone in choosing Course 7 because of 7.03.

“Genetics has this interesting force, especially in MIT biology. The department’s historical — and active — role in genetics research ties directly into the way the course is taught,” Lee says. “Biology is about logic, scientific reasoning, and posing the right questions.”

A few years later, as a teaching assistant for class  7.002 (Fundamentals of Experimental Molecular Biology ), he came to value how much care MIT biology professors take in presenting the material for all offered courses.

“I really appreciate how much effort MIT professors put into their teaching,” Lee says. “As a TA, you realize the beauty of how the professors organize these things — because they’re teaching you in a specific way, and you can grasp the beauty of it — there’s a beauty in studying and finding the patterns in nature.”

An undertaking to apply

To attend MIT at all hadn’t exactly been a lifelong dream. In fact, it didn’t occur to Lee that he could or should apply until he represented South Korea at the 49th International Chemistry Olympiad, where he won a Gold Medal in 2017. There, he had the chance to speak with MIT alumni, as well as current and aspiring students. More than half of those aspiring students eventually enrolled, Lee among them.

“Before that, MIT was this nearly mythical institution, so that experience really changed my life,” Lee recalls. “I heard so many different stories from people with so many different backgrounds — all converging towards the same enthusiasm towards science.” 

At the time, Lee was already attending medical school — a six-year undergraduate program in Korea — that would lead to a stable career in medicine. Attending MIT would involve both changing his career plans and uprooting his life, leaving all his friends and family behind.

His parents weren’t especially enthusiastic about his desire to study at MIT, so it was up to Lee to meet the application requirements. He woke up at 3 a.m. to find his own way to the only SAT testing site in South Korea — an undertaking he now recalls with a laugh. In just three months, he had gathered everything he needed; MIT was the only institution in the United States Lee applied to.

He arrived in Cambridge, Massachusetts, in 2018 but attended MIT only for a semester before returning to Korea for his two years of mandatory military service.

“During military service, my goal was to read as many papers as possible, because I wondered what topic of science I’m drawn to — and many of the papers I was reading were authored by people I recognized, people who taught biology at MIT,” Lee says. “I became really interested in cancer biology.”

Return to MIT

When he returned to campus, Lee pledged to do everything he could to meet with faculty and discuss their work. To that end, he joined the MIT Undergraduate Research Journal , allowing him to interview professors. He notes that most MIT faculty are enthusiastic about being contacted by undergraduate students.

Stateside, Lee also reached out to Michael Lawrence , an assistant professor of pathology at Harvard Medical School and assistant geneticist at Mass General Cancer Center, about a preprint concerning APOBEC, an enzyme Lee had studied at Seoul National University. Lawrence’s lab was looking into APOBEC and cancer evolution — and the idea that the enzyme might drive drug resistance to cancer treatment.

“Since he joined my lab, I’ve been absolutely amazed by his scientific talents,” Lawrence says. “Hanjun’s scientific maturity and achievements are extremely rare, especially in an undergraduate student.”

Lee has made new discoveries from genomic data and was involved in publishing  a paper in Molecular Cell and  a paper in Nature Genetics . In the latter, the lab identified the source of background noise in chromosome conformation capture experiments, a technique for analyzing chromatin in cells.

Lawrence thinks Lee “is destined for great leadership in science.” In the meantime, Lee has gained valuable insights into how much work these types of achievements require.

“Doing research has been rewarding, but it also taught me to appreciate that science is almost 100 percent about failures,” Lee says. “It is those failures that end up leading you to the path of success.”

Widening the scope

Lee’s personal motto is that to excel in a specific field, one must have a broad sense of what the entire field looks like, and suggests other budding scientists enroll in courses distant from their research area. He also says it was key to see his peers as collaborators rather than competitors, and that each student will excel in their own unique way.

“Your MIT experience is defined by interactions with others,” Lee says. “They will help identify and shape your path.”

For his accomplishments, Lee was recently named an  American Association for Cancer Research Undergraduate Scholar . Last year, he also spoke at the Gordon Research Conference on Cell Growth and Proliferation about his work on the retinoblastoma gene product RB.

Encouraged by positive course evaluations during his time as a TA, Lee hopes to inspire other students in the future through teaching. Lee has recently decided to pursue a PhD in cancer biology at Harvard Medical School, although his interests remain broad.

“I want to explore other fields of biology as well,” he says. “I have so many questions that I want to answer.”

Although initially resistant, Lee’s mother and father are now “immensely proud to be MIT parents” and will be coming to Cambridge in May to celebrate Lee’s graduation.

“Throughout my years here, they’ve been able to see how I’ve changed,” he says. “I don’t think I’m a great scientist, yet, but I now have some sense of how to become one.” 

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