★ 178 · Updated 2026-06-30
Detect SNPs and indels from aligned reads using bcftools mpileup and call pipeline, generating VCF output from BAM files.
Browse skills that share this tag.
★ 178 · Updated 2026-06-30
Detect SNPs and indels from aligned reads using bcftools mpileup and call pipeline, generating VCF output from BAM files.
★ 119 · Updated 2026-06-15
Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences for NGS pipelines
★ 359 · Updated 2026-06-15
Read and write genomic alignment, variant, and sequence files for NGS data processing