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BCFTOOLS Tutorial for processing vcfs - episode 1 (Bioinformatics for Beginners) View | |
bcftools tutorial | bcftools view | count the number of variants per chromosome in a VCF file (Bioinformatics for Beginners) View | |
Bcftools tutorial on How to read VCF files | indexing VCFs (Bioinformatics Coach) View | |
Bcftools tutorial | bcftools Split a VCF file into snps and indels (Bioinformatics Coach) View | |
A bioinformatics tutorial on how to merge multiple vcfs using bcftools (Bioinformatics Coach) View | |
Bcftools concat to Merge or combine Chromosome VCF files (Bioinformatics for Beginners) View | |
bcftools query command | Extract and view chromosome names in a VCF file (Bioinformatics for Beginners) View | |
Bioinformatics Talks | Variant calling using bcftools (Data Science Coach) View | |
How to Filter High Quality Variants using BCFTOOLS | VCF files (Bioinformatics Coach) View | |
123VCF: Intuitive and Efficient Tool for Filtering VCF files (English version) (AD Bioinformatics) View |