Topic: vcf Goto Github
Some thing interesting about vcf
Some thing interesting about vcf
vcf,Structural variant toolkit for VCFs
User: acenglish
vcf,machine learning for genomic variants
Organization: aehrc
Home Page: http://bioinformatics.csiro.au/variantspark
vcf,VCF-kit: Assorted utilities for the variant call format
Organization: andersenlab
Home Page: http://www.andersenlab.org
vcf,tools for reading, writing, merging, and remapping SNPs
User: apriha
vcf,convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
User: arrogantrobot
vcf,A fluent builder class for vCard files.
Organization: astrotomic
vcf,Python 3 library with good support for both reading and writing VCF
Organization: bihealth
vcf,Syntax highlighting for computational biology
Organization: biosyntax
Home Page: http://bioSyntax.org
vcf,useful command-line tools written to showcase hts-nim
User: brentp
Home Page: https://github.com/brentp/hts-nim
vcf,annotate a VCF with other VCFs/BEDs/tabixed files
User: brentp
Home Page: https://genomebiology.biomedcentral.com/articles/10.1186/s13059-016-0973-5
vcf,Annotation of VCF variants with functional impact and from databases (executable+library)
Organization: charite
Home Page: http://jannovar.readthedocs.io/en/master/
vcf,Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
Organization: chasewnelson
vcf,Learning the Variant Call Format
User: davetang
Home Page: https://davetang.github.io/learning_vcf_file/
vcf,Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
User: edgardomortiz
vcf,A python parser to simplify and build the VCF (Variant Call Format).
User: everestial
vcf,Toolset for SV simulation, comparison and filtering
User: fritzsedlazeck
vcf,Haplotype VCF comparison tools
Organization: illumina
vcf,Graph realignment tools for structural variants
Organization: illumina
vcf,This vCard PHP library can easily parse or generate/export vCards as .vcf
User: jeroendesloovere
Home Page: https://packagist.org/packages/jeroendesloovere/vcard
vcf,A not so forgiving vCard / vcf parser
User: jhermsmeier
vcf,Genome browser and variant annotation
User: kcleal
vcf,A standalone and free application to explore genetics variations from VCF file
Organization: labsquare
Home Page: https://cutevariant.labsquare.org/
vcf,convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations
User: plantimals
vcf,The Polykit X1 is a DIY semi-modular, analog, patchable synthesizer
User: polykit
vcf,Convert Telegram Contacts JSON File to VCF File
User: s-nikravesh
vcf,Cancer Predisposition Sequencing Reporter (CPSR)
User: sigven
Home Page: https://sigven.github.io/cpsr/
vcf,Personal Cancer Genome Reporter (PCGR)
User: sigven
Home Page: https://sigven.github.io/pcgr
vcf,Application of pan-genome for population
User: starskyzheng
vcf,Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
User: tariqdaouda
Home Page: http://pygeno.iric.ca
vcf,Efficient variant-call data storage and retrieval library using the TileDB storage library.
Organization: tiledb-inc
Home Page: https://tiledb-inc.github.io/TileDB-VCF/
vcf,vcfdist: Accurately benchmarking phased variant calls
User: timd1
vcf,:scissors: :zap: Rapid haploid variant calling and core genome alignment
User: tseemann
vcf,vembrane filters VCF records using python expressions
Organization: vembrane
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