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)
Udemy
platform
English
language
Other
category
Bioinformatics: Learn NGS Data Analysis From Scratch
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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