vcf

Cloud-native genomic dataframes and batch computing

C library for high-throughput sequencing data formats

✂️ ⚡ Rapid haploid variant calling and core genome alignment

a calendar server aiming to be simple, fast and passwordless

This vCard PHP library can easily parse or generate/export vCards as .vcf

Haplotype VCF comparison tools

cython + htslib == fast VCF and BCF processing

Structural variant toolkit for VCFs

Toolset for SV simulation, comparison and filtering

Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms

annotate a VCF with other VCFs/BEDs/tabixed files

Genome browser and variant annotation

Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis

Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs

A Java API for high-throughput sequencing data (HTS) formats.

Personal Cancer Genome Reporter (PCGR)

Syntax highlighting for computational biology

A framework for state-of-the-art pre-trained bio foundation models on genomics and transcriptomics modalities.

A collection of scripts and notes related to genomics and bioinformatics

The Pharmacogenomic Clinical Annotation Tool