Thu, Oct 22, 2026Fall (Semester 1) · Week 9Day 42 of 7580-min block

Karyotype and inheritance notes

Today's target

Students take structured notes on chromosomal structure, karyotyping, and patterns of inheritance, then complete the PLTW online task.

Due today · Notebook check Required

Annotated notes on karyotype structure, aneuploidy, and inheritance patterns with a labeled karyotype diagram.

Your 4 steps today
  1. 1
    Do this
    Students take structured notes on chromosomal structure, karyotyping, and patterns of inheritance, then complete the PLTW online task.
  2. 2
  3. 3
    Submit this
    Notebook check: Annotated notes on karyotype structure, aneuploidy, and inheritance patterns with a labeled karyotype diagram.
  4. 4
    Submit it here
    1. 1CMSD website. Go to clevelandmetroschools.org and click the Clever button.
    2. 2Clever. Clever opens. Sign in if it asks.
    3. 3Microsoft (district) login. Use your district Microsoft account (the one for school).
    4. 4Schoology. Open Schoology, then your class, then Assignments, and find the file named below.
    The file to submit is named: Principles of Biomedical Technology (Principles of Biomedical Science) › Unit 2.2 to 2.3: Chromosomal abnormalities, genetic risk, family evidence, diagnosis from mixed data. › Notebook check
    Open Schoology
Were you absent? Jump to the make-up plan
Where this fits
Tested on (Ohio WebXam)
Principles and Practice of Biomedical Technology · 072110
PLTW lesson
PBS · Karyotype and inheritance notes
WebXam domain
Biotechnology Research and Experiments
Evidence to produce
Notebook check
Quick glossary
CER:
Claim, Evidence, Reasoning — make a claim, back it with evidence, explain your reasoning.
SOP:
Standard Operating Procedure — the exact steps to follow (especially in a lab).
Tracker:
Your PLTW progress log where you record completed evidence.
myPLTW:
The PLTW course site where you do the online activities — you open it through Schoology.
Learn first

Minute-by-minute · 80-minute block

💡 Big idea: The structure of chromosomes and patterns of inheritance determine how genetic variation and disease risk pass from parent to child.

  1. 0-5 minWarm-up: sketch what you think a stained chromosome spread looks like.
  2. 5-30 minTeacher-led notes: chromosome number, autosomes, sex chromosomes, karyotype construction.
  3. 30-50 minNotes continued: aneuploidy examples, dominant/recessive/carrier definitions, pedigree reading.
  4. 50-72 minPLTW online activity on chromosomal abnormalities (individual, self-paced).
  5. 72-80 minExit check: label a blank karyotype diagram with three correct annotations.
Mr. Mendoza's 5-minute intro
  • Notes today are the backbone for Wednesday's hands-on karyotype analysis.
  • Pay attention to how scientists actually read a karyotype in a clinical lab.
  • The WebXam 072110 Biotechnology strand tests chromosome structure and inheritance directly.
  • Finish the PLTW online activity before the period ends so Wednesday's lab makes sense.
Do this, step by step
  1. 1Annotate teacher notes on chromosome number, autosomes, and sex chromosomes.
  2. 2Diagram how a karyotype is built from a stained metaphase spread.
  3. 3Distinguish aneuploidy (such as trisomy 21) from normal diploid karyotypes.
  4. 4Define dominant, recessive, and carrier as used in a pedigree.
  5. 5Complete the assigned PLTW online activity on chromosomal abnormalities.
You'll be able to
  • Correctly label autosomes, sex chromosomes, and one trisomy on a karyotype.
  • Submit the PLTW online task with all responses complete.
Know by the end
  • A karyotype organizes chromosomes by size and centromere position to reveal numerical abnormalities.
  • Dominant and recessive alleles follow predictable inheritance patterns visible in pedigrees.
  • Aneuploidy, such as trisomy 21, arises from nondisjunction during meiosis.
📺 Tutor me: MedlinePlus: How are chromosome changes inherited?
Do the work

Your PLTW work today

Open this PLTW section today

Unit 2.2 to 2.3: Chromosomal abnormalities, genetic risk, family evidence, diagnosis from mixed data. · Karyotype and inheritance notes

Day 2 of this lesson. Open this exact section in myPLTW (reached through Schoology), then do the work below.

Do this: Open myPLTW, navigate to Lesson 2.2 Decoding a Diagnosis, and find the chromosomal abnormalities online activity.

Complete

Complete all questions and submit within myPLTW before end of period.

How far to get

You submitted the bioethics reflection Monday. Today finish the full chromosomal abnormalities activity so Wednesday's karyotype lab makes sense.

Upload as evidence

Show the completion screen or checkmark to the teacher before packing up.

All PLTW activities are completed inside the PLTW course environment — this page only gives direction. Submit producibles on Schoology.

The plan

Today's PLTW tracker

Check things off as you work, then submit. This tells Mr. Mendoza how you're doing so he can help the class. It does not replace turning in your producible on Schoology.

Use the code Mr. Mendoza gave you, not your name. Saved on this device.

Unit 2.2 to 2.3: Chromosomal abnormalities, genetic risk, family evidence, diagnosis from mixed data.Day 2 of this projectSee the full week plan
Today's PLTW target

Unit 2.2 to 2.3: Chromosomal abnormalities, genetic risk, family evidence, diagnosis from mixed data. · Karyotype and inheritance notes

Open myPLTW, navigate to Lesson 2.2 Decoding a Diagnosis, and find the chromosomal abnormalities online activity.

You submitted the bioethics reflection Monday. Today finish the full chromosomal abnormalities activity so Wednesday's karyotype lab makes sense.

This is how Mr. Mendoza sees the class keeping pace with PLTW. Be honest, it only helps if it is accurate.

1 · What you do today

🎯 Students take structured notes on chromosomal structure, karyotyping, and patterns of inheritance, then complete the PLTW online task.

  • Annotate teacher notes on chromosome number, autosomes, and sex chromosomes.
  • Diagram how a karyotype is built from a stained metaphase spread.
  • Distinguish aneuploidy (such as trisomy 21) from normal diploid karyotypes.
  • Define dominant, recessive, and carrier as used in a pedigree.
  • Complete the assigned PLTW online activity on chromosomal abnormalities.
2 · Turn in today

Notebook check: Annotated notes on karyotype structure, aneuploidy, and inheritance patterns with a labeled karyotype diagram.

Submit on Schoology

Upload by 11:29 PM for full credit.

3 · Who's doing what (team)
TaskWho
Annotate teacher notes on chromosome number, autosomes, and sex chromosomes._______
Diagram how a karyotype is built from a stained metaphase spread._______
Distinguish aneuploidy (such as trisomy 21) from normal diploid karyotypes._______
Define dominant, recessive, and carrier as used in a pedigree._______
Complete the assigned PLTW online activity on chromosomal abnormalities._______

Working solo? Put your own name in "Who" for every row.

4 · Words I can use correctly
5 · I'm successful today when I can…
  • Correctly label autosomes, sex chromosomes, and one trisomy on a karyotype.
  • Submit the PLTW online task with all responses complete.
6 · Reflection & next steps
Where are you today?0/7 checked
Pick your period and code first.
Words

This unit's vocabulary

karyotypeinheritancegenotype/JEE-noh-type/phenotype/FEE-noh-type/carrierpedigree/PED-ih-gree/genetic risk

Tap the speaker to hear a term. Weekly vocabulary task: add two of these terms to your notebook glossary with a definition and an example in your own words.

Check yourself

WebXam practice

Tap an answer to check it · nothing is recorded or graded
A karyotype shows three copies of chromosome 21. What does this finding indicate?
Two carrier parents each carry one recessive allele. What is the probability that a child inherits both recessive alleles?
A genetic test reports a result without listing its false-positive rate. Why does that limit an evidence-based conclusion?
Check yourself

Cumulative WebXam review

A quick mixed-review pulling questions from earlier units plus today, so the WebXam material stays fresh.

Tap an answer to check it · nothing is recorded or graded
[Review: Talk to Your Doc: clinical communication and vital signs] What is the purpose of an experiment measuring blood glucose after a drug or a placebo?
[Review: Clinical Data: reading bloodwork and monitoring chronic disease] A monitoring table shows one glucose value far outside the others in a steady dataset. What is the best first action?
[Review: Decoding a Diagnosis: from DNA to protein] A bacterial transformation produces zero colonies even though the protocol was followed. Which is the most likely cause?
A karyotype shows three copies of chromosome 21. What does this finding indicate?
Explore

Where this leads — careers

Safety net

What to do if you were absent

If YOU are absent

Today is individual PLTW work, so do exactly what we did in class, from home: complete the same PLTW target above, then submit your Notebook check.

Open Schoology (CMSD) and keep going

How to get there: open the CMSD website, click Clever, sign in with your Microsoft (district) account, then open Schoology from Clever.

If MR. MENDOZA is absent

Class still runs. Complete the online activity above (it's self-guided). Need the concept taught without a teacher? Use this authoritative explainer:

NHGRI genome.gov
Explore

Optional extra credit (async)

You've passed Unit 2, so the optional extra-credit track is open. Complete reserved-unit work from home (virtual labs included) for extra credit, all submitted on Schoology.

Open the extra-credit track
How this is graded
For: Notebook check — Annotated notes on karyotype structure, aneuploidy, and inheritance patterns with a labeled karyotype diagram.
  • Complete
    Every required part of the artifact is present, nothing left blank.
  • Accurate
    The science and the data are correct and match the evidence.
  • Scientific reasoning
    You explain your claim with evidence and reasoning (CER), not just an answer.
  • Professional communication
    Clear, organized, labeled, and written the way a clinician or scientist would.
  • Submitted
    Turned in the right way (Schoology for routine work) and confirmed.
Submission Zone

Drop your Thu, Oct 22, 2026 · Karyotype and inheritance notes here. Use a clear file name (your initials + project). Routine work still goes to Schoology (via the CMSD portal).

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