The Definitive Beginner’s Guide to Personal Genomics & DNA Interpretation

Unlock the secrets in your DNA without drowning in jargon or expensive software.

Turn Raw DNA Files into Clear, Actionable Insights — Even if You’re New to Genetics!

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4.9/5 star reviews

Thousands of happy customers worldwide

AS SEEN ON

Unlock Your DNA and Inform Health Decisions

Does this sound like you?

  • Overwhelmed by the sheer volume of genomic data.

  • Unsure which tools or databases to trust.

  • Difficulty distinguishing benign variants from pathogenic ones.

  • Concerned about misinterpreting results and causing harm.

  • Spending hours on Google with little progress.

  • Confidently navigate raw DNA files and annotation tools.

  • Use ACMG guidelines to classify variants accurately.

  • Produce professional genomic reports with our ready-to-use templates.

  • Save money by relying only on the essential software we recommend.

  • Position yourself as the local genomics expert and attract clients.

What’s Included in Your Enrollment

Genetics Fundamentals

Gain a foundational understanding of DNA, genes, and variation—the building blocks of genomics.

Managing Raw Genomic Data

Learn to obtain, format, and QC raw genome and exome files from popular consumer and clinical platforms.

Variant Annotation Techniques

Master free bioinformatics tools to annotate variants and link them to known databases.

Assessing Disease Risk

Use accepted guidelines (ACMG) to classify variants and calculate disease risk.

Pharmacogenomics Essentials

Identify drug–gene interactions that influence dosage and adverse reactions.

Ancestry & Trait Analysis

Explore population genetics to reveal ancestry segments and trait predictions.

TESTIMONIALS

What our students are saying...

" Coming from a nursing background, I was intimidated by genomics. This course broke it down beautifully—now I help my clinic interpret pharmacogenomic tests. "

- Grace Williams, RN

" As a software engineer building a health app, I needed to understand DNA data. The practical labs saved me months of research. "

- John Doe

" I’ve doubled my income by offering personalized ancestry reports after taking this program. The community support is incredible. "

- Roberta Johnson

MODULES

FOLLOW MY STEP BY STEP VIDEO TRAINING

Genetics Fundamentals

Gain a foundational understanding of DNA, genes, and variation—the building blocks of genomics.

Managing Raw Genomic Data

Learn to obtain, format, and QC raw genome and exome files from popular consumer and clinical platforms.

Variant Annotation Techniques

Master free bioinformatics tools to annotate variants and link them to known databases.

Assessing Disease Risk

Use accepted guidelines (ACMG) to classify variants and calculate disease risk.

Pharmacogenomics Essentials

Identify drug–gene interactions that influence dosage and adverse reactions.

Ancestry & Trait Analysis

Explore population genetics to reveal ancestry segments and trait predictions.

Ethics & Privacy in Personal Genomics

Navigate privacy laws, consent, and responsible disclosure of sensitive findings.

Reporting & Communication Skills

Transform complex results into clear reports and conversations clients understand.

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4.9/5 star reviews

Learn to Decode Your Genome Like a Pro

A step-by-step online program that teaches you how to read raw DNA data, identify meaningful variants, and translate findings into actionable insights.

Here's what you get:

  • Instant access to 40 bite-sized HD video lessons.

  • Downloadable cheat sheets, variant interpretation templates, and code notebooks.

  • Membership to a private Slack community of genetic enthusiasts and experts.

  • Lifetime updates as the science and software evolve.

Today Just

$997 one time

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"Best purchase ever!"

" As a software engineer building a health app, I needed to understand DNA data. The practical labs saved me months of research. "

ABOUT YOUR INSTRUCTOR

Meet Jennifer

Dr. Amelia Chen is a clinical geneticist and bioinformatics researcher with 12 years of experience translating genomic data into patient-centered reports. After earning her PhD at Stanford, she has helped thousands of people make sense of their DNA.

While reviewing countless direct-to-consumer DNA reports, she realized most people receive raw data with no guidance. Determined to close this gap, she built an accessible curriculum that demystifies genomics and empowers informed decision-making.

Graduates now work in genetic counseling, biotech, and personalized medicine; many have leveraged their new skills to launch side consultancies reading DNA reports for clients.

  • Lead author on 20+ peer-reviewed papers in human genomics.

  • Advisor to two leading consumer genetics companies.

  • Taught genomics workshops at Harvard, MIT, and UCSF.

  • Recipient of the National Science Foundation Early-Career Award.

  • Featured speaker at the American College of Medical Genetics annual meeting.

  • Mentored over 5,000 students through online genomics courses.

WHO IS THIS FOR...

Perfect for healthcare professionals, researchers, and curious individuals who want to understand personal genomics without a PhD.

Healthcare Professionals

Genetic Counselors in Training

Bioinformatics Beginners

Pharmacists

Biomedical Researchers

Data Scientists Exploring Genomics

Direct-to-Consumer DNA Enthusiasts

Students Pursuing Life Sciences

STILL NOT SURE?

Satisfaction guaranteed

We want you to find value in our trainings! We offer full refunds within 30 days. With all of our valuable video training, we are confident you WILL love it!

STILL GOT QUESTIONS?

Frequently Asked Questions

Do you teach bioinformatics coding?

Absolutely. We provide beginner-friendly Jupyter notebooks in Python and R but also show point-and-click alternatives—no prior coding required.

Do I need a science degree to take this course?

No. We start with the fundamentals and build up. Basic computer skills and curiosity are all you need.

How is this course different from reading free articles online?

We combine up-to-date science, real datasets, and mentorship. Instead of piecemeal information, you get a structured roadmap tested on thousands of students.

Enroll in the course now!

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