Cloud-native genomic dataframes and batch computing
C library for high-throughput sequencing data formats
This vCard PHP library can easily parse or generate/export vCards as .vcf
:scissors: :zap: Rapid haploid variant calling and core genome alignment
Haplotype VCF comparison tools
cython + htslib == fast VCF and BCF processing
Convert a VCF into a MAF, where each variant is annotated to only one of...
annotate a VCF with other VCFs/BEDs/tabixed files
Toolset for SV simulation, comparison and filtering
Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
Structural variant toolkit for VCFs
A Java API for high-throughput sequencing data (HTS) formats.
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alig...
Syntax highlighting for computational biology
Personal Cancer Genome Reporter (PCGR)