Learn essential bioinformatics skills in this comprehensive tutorial covering various aspects of handling genomic data. Explore techniques for merging multiple VCF files using bcftools, reading and counting sequences in FASTA files, and efficiently working with VCF files. Master the process of indexing VCFs and gain proficiency in reading VCF files using bcftools. Discover how to count the number of variants in a VCF file using Linux commands. Perfect for beginners in bioinformatics, this course provides practical knowledge for working with genomic data formats and tools commonly used in the field.
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
