This course teaches students how to merge multiple VCF files using bcftools, read and count sequences in a FASTA file, index VCFs, and count the number of variants in a VCF file. The teaching method includes tutorials on using Linux for bioinformatics and bcftools. The intended audience for this course is beginners in bioinformatics looking to enhance their data handling skills.
Overview
Syllabus
A bioinformatics tutorial on how to merge multiple vcfs using bcftools.
Linux for Bioinformatics | How to Read and Count Sequences in a FASTA file | Beginners Course.
How to read VCF files using bcftools | indexing VCFs.
How to read VCF files using bcftools tutorial | Bioinformatics for Beginners | Course.
Linux for Bioinformatics | How to count the number variants in a VCF file | Beginners Course.
Taught by
Bioinformatics Coach
