DNA-Seq in Cancer Genomics: Variant Detection in Breast Cancer
Unlock the secrets of the cancer genome in this intensive, hands-on crash course. Transition from raw FASTQ files to identifying actionable mutations (SNVs, Indels, and CNVs) specifically in Breast Cancer datasets. Whether you are a biologist looking to go dry-lab or a data scientist entering oncology, this course provides the industry-standard pipeline (GATK, BWA, VEP) needed to drive precision medicine.
- 5.0/5
- English
- Updated Oct 2026
₹6000
$80
Indian learners pay in INR; international learners are billed in USD.
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About this course
The DNA-Seq in Cancer Genomics: Variant Detection in Breast Cancer at Dr. Omics Edu is a live, mentor-led online course in cancer bioinformatics and genomics. It uses a breast cancer dataset to teach DNA-seq variant detection end to end. You learn on real biological data and finish with a cancer genomics analysis on a real dataset that you can show to an employer, a guide or an admissions panel.
In this course you move through cancer genomics and dna-seq fundamentals, quality control and alignment and variant calling on breast cancer data, then apply them in a hands-on project. The course runs live online across 1 module, so you can ask your mentor questions as you work. It is open to learners at every level, and the mentor adjusts the pace to your background.
What you will learn
Skills you will gain
Certification
Available
Issued by Dr. Omics EduCourse curriculum
1 moduleWhat you need to start
- Biology: Basic understanding of DNA structure and the central dogma.
- Technical: Familiarity with the Linux command line (e.g., cd, ls, grep) is recommended but not mandatory (introductory materials provided).
- Hardware: A laptop with at least 8GB RAM (Cloud-based servers will be provided for heavy processing).
Who this course is for
- B.Sc, M.Sc, B.Tech, M.Tech, MBBS, B.Pharm and PhD students and researchers in biotechnology, oncology, genetics or life sciences.
