”vcf“ 的搜索结果

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

C++ library and cmdline tools for parsing and manipulating VCF files with python and zig bindings

A set of tools written in Perl and C++ for working with VCF files, such as those generated by the 1000 Genomes Project.

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

A Floating Action Button just like Google inbox for iOS

Tools to work with variant call format files

Haplotype VCF comparison tools

A Variant Call Format reader for Python.

annotate a VCF with other VCFs/BEDs/tabixed files

VCF visualization interface

Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently

Smart VCF parser DSL

cython + htslib == fast VCF and BCF processing

Convert GWAS summary statistics to VCF

A not so forgiving vCard / vcf parser

convert VCF to HMP format

vembrane filters VCF records using python expressions

CEM3350/AS3350 based 8 channel VCF

Validation suite for Variant Call Format (VCF) files, implemented using C++11

VCF-kit: Assorted utilities for the variant call format

create a gemini-compatible database from a VCF

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

Reading, querying and writing GWAS summary data in VCF format

genotype :: ped correspondence check, ancestry check, sex check. directly, quickly on VCF

Query sequence data (VCF/BCF1/BCF2, Tabix, BGEN, PLINK) in R

convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf