Bioinformatics: Learn NGS Data Analysis From Scratch
Best Bioinformatics course to Learn Bioinformatics NGS Variant Calling Data Analysis from Scratch (Theory & Practical)
4.55 (82 reviews)

338
students
4.5 hours
content
Jun 2025
last update
$19.99
regular price
What you will learn
You will learn the fundamentals of Molecular Biology From Genotype to Phenotype
You will installation of Linux in Windows (WSL) and fundamentals of bash scripting
You will learn about the FASTQ and FASTA file formats
You will learn the installation of tools for Variant Calling in Linux
You will learn the GATK best practice pipeline for Variant calling starting from FASTQ to VCF
You will learn the structure of VCF file and understanding of its information
You will learn about Annotations of Variants present in FASTQ file using Funcotator
You will learn the sorting of Annotated VCF file to take clinical decisions
You will learn how to leverage the open source software to analyze the NGS data
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6164051
udemy ID
03/09/2024
course created date
01/08/2025
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