There are 1 repository under vcf-files topic.
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
Learning the Variant Call Format
Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
Rapid standardisation and quality control of GWAS or QTL summary statistics
A python parser to simplify and build the VCF (Variant Call Format).
A phenotype-based tool for variant prioritization in WES and WGS data
create a interactive coverage plot dashboard from bam files and add gb, vcf and bed tracks
A full-featured Python package for parsing and creating iCalendar and vCard files
Accelerate the generation of personalized proteomes from a Variant calling format (VCF) file and a reference proteome using graphical processing units (GPUs).
Read and write VCF and BCF files
Evolutionary Bioinformatics Toolkit (EBT)
A fast and scalable CUDA implementation to conduct highly parallelized evolutionary tests on large scale genomic data.
Collection of simple C scripts for parsing vcf or bam files using the htslib C library. These scripts can be used as the starting point for more complex scripts
Visualize microbial evolution at the SNP level!
A simple Python script for extracting images out of an "SMS Backup & Restore" backup.
Genotype likelihood simulator for VCF/BCF files
Converts phonebook Fritzbox between .xml <=> .csv or .vcf (webapp) ; DE: konvertiert Telefonbuch Datei
A utility to merge a large number of VCF files incrementally
This Utility software converts VCF files into CSV format as an Excel sheet.
A .NET vCard parser with Android contacts2.db and MeCard support
API to read, write, and filter DNA sequence alignment files
A python library to develop genomic data simulators