vcflib is a C++ library and suite of command-line tools for parsing, filtering, merging, annotating, and transforming VCF (Variant Call Format) files. Use when users need to filter variants by INFO/FO
Use with AI
Install the MCP server or CLI to instantly fetch vcflib documentation:
Install command
claude mcp add biocontext7 -- npx @biocontext7/mcpOr share this page: biocontext7.com/tools/vcflib
AGAT (Another Gff Analysis Toolkit) — comprehensive Perl toolkit for reading, writing, validating, fixing, and manipulating genome annotation files in GFF3, GTF, and GFF2 formats. Converts between for
1 shared topic • 2 shared operations
Limnology (freshwater science) — computational toolkit for freshwater ecosystem analysis including lake thermal stratification (rLakeAnalyzer), lake metabolism estimation (LakeMetabolizer), eDNA metab
1 shared topic • 2 shared operations
Use when performing GWAS fine-mapping with PAINTOR (Probabilistic Annotation INTegratOR). Computes posterior inclusion probabilities (PIPs) for causal variants by integrating summary statistics (Z-sco
1 shared topic • 2 shared operations
Use when working with PolyFun — functionally-informed polygenic fine-mapping from GWAS summary statistics. Computes per-SNP heritability priors using S-LDSC with functional annotations, then runs SuSi
1 shared topic • 2 shared operations
RTG Tools — Java-based toolkit from Real Time Genomics for haplotype-aware variant call comparison, VCF filtering, statistics, and pedigree analysis. Primary use: vcfeval for benchmarking variant call
1 shared topic • 2 shared operations