Bioinformatics: Learn NGS Data Analysis From Scratch

Best Bioinformatics course to Learn Bioinformatics NGS Variant Calling Data Analysis from Scratch (Theory & Practical)

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Bioinformatics: Learn NGS Data Analysis From Scratch

Bioinformatics: Learn NGS Data Analysis From Scratch udemy course

Best Bioinformatics course to Learn Bioinformatics NGS Variant Calling Data Analysis from Scratch (Theory & Practical)

Become a Bioinformatics Pro with Hands-On NGS Data Analysis Skills!

Next-Generation Sequencing (NGS) is transforming healthcare, research, and biotechnology. With bioinformatics expertise now essential for biologists, clinicians, and researchers, this Udemy course empowers you to analyse human genomic data like a pro using the GATK pipeline (Genome Analysis Toolkit). Master industry-standard workflows to process FASTQ files, call variants, annotate VCFs, and unlock insights for personalised medicine, cancer genomics, and rare disease research.

Why This Course?

  • Ranked #1 Skill in Genomics: Bioinformatics is critical for interpreting NGS data. Stand out in academia, pharma, or clinical labs.

  • Zero to Pipeline Mastery: No prior coding experience needed! Learn end-to-end NGS analysis for human genomes (WGS/WES).

  • GATK-Certified Workflows: Follow best practices endorsed by the Broad Institute for accurate, reproducible results.

  • Career-Ready Projects: Analyse real datasets, annotate variants with Funcotator, and build a portfolio for job applications.

5 Modules to Master NGS Bioinformatics:
Bioinformatics Basics for Biologists: DNA, RNA, genomic variations, and sequencing fundamentals.
NGS Technologies & Data Generation: Illumina, and data formats (FASTQ, BAM, VCF).
GATK Pipeline: FASTQ → BAM → VCF: Quality control, alignment (BWA), duplicate removal, and variant calling.
VCF File Mastery: Interpret variants, filter low-quality calls, and prioritise clinically relevant mutations.
Funcotator for VCF Annotation: Predict functional impacts (pathogenic vs. benign) and generate clinical reports.

Who Should Enrol?

  • Biologists & Clinicians: Analyse genomic data without relying on bioinformaticians.

  • Researchers: Publish robust findings using reproducible NGS workflows.

  • Students: Boost employability with in-demand bioinformatics skills.

  • Biotech Professionals: Upskill for roles in precision medicine, oncology, or diagnostics.

What’s Included?
Downloadable Workflows: Automate analysis with ready-to-use scripts.
Practice Datasets: Human genomic data
Certificate of Completion: Showcase your skills on LinkedIn/resumes.
Lifetime Access: Stay updated with NGS advancements.

Disclaimer: Focused on human genomic data (WGS/WES). Microbial workflows differ and are not covered.