Topic: variant-annotation Goto Github
Some thing interesting about variant-annotation
Some thing interesting about variant-annotation
variant-annotation,A tool for prioritising identity-by-descent (IBD) variants in Whole Genome Sequencing (WGS) data from families with rare heritable diseases.
User: a-thind
variant-annotation,Variant Calling and Annotation using PacBio Hi-Fi Reads
User: anand-imcm
variant-annotation,Library for indexing VCF files for random access searches by rsID
Organization: bioforensics
variant-annotation,Neighborhood-Aware Variant Impact Predictor
User: bpucker
variant-annotation,Analysis pipleine to model tumour clonal evolution from WGS data (driver annotation, quality control of copy number calls, subclonal and mutational signature deconvolution)
Organization: caravagnalab
variant-annotation,Pipeline for variant annotation using Variant Effect Predictor (VEP)
Organization: cerc-genomic-medicine
variant-annotation,Annotation of VCF variants with functional impact and from databases (executable+library)
Organization: charite
Home Page: http://jannovar.readthedocs.io/en/master/
variant-annotation,The DKFZ-ODCF, formerly DKFZ/eilslabs SNV-Calling Workflow
Organization: dkfz-odcf
variant-annotation,A flexible variant annotator written in Python
User: elscalzarotodoc
variant-annotation,A python parser to simplify and build the VCF (Variant Call Format).
User: everestial
variant-annotation,OpenCRAVAT as a GenePattern module
Organization: genepattern
variant-annotation,2019 Genomics Epidemiology Workshop at Academia Sinica
User: geniusphil
Home Page: https://gew2019.genomics.sinica.edu.tw/
variant-annotation,💻 Command line interface for Genome Nexus 🧬
Organization: genome-nexus
Home Page: https://www.genomenexus.org
variant-annotation,GPF: Genotypes and Phenotypes in Families
Organization: iossifovlab
variant-annotation,A modular annotation tool for genomic variants
Organization: karchinlab
variant-annotation,shiny web-app
User: kopalgarg
variant-annotation,Annotate genomics variations of hg19 by using a BED format database, which construct from NCBI annotation release 104
User: ltnetcase
variant-annotation,
User: matmu
Home Page: http://genehopper.de/qtlizer
variant-annotation,Call and score variants from WGS/WES of rare disease patients.
Organization: nf-core
Home Page: https://nf-co.re/raredisease
variant-annotation,Clinical Whole Genome and Exome Sequencing Pipeline
Organization: openomics
Home Page: https://openomics.github.io/genome-seek/
variant-annotation,Automated statistical and functional fine-mapping pipeline with extensive API access to datasets.
Organization: rajlabmssm
Home Page: https://rajlabmssm.github.io/echolocatoR
variant-annotation,Human mitochondrial variants annotation using HmtVar.
User: robertopreste
Home Page: https://hmtnote.readthedocs.io
variant-annotation,A tool for analysis of genomic variants in human genomes.
User: sevcandogramaci
variant-annotation,Add functional variant annotation to MAF file
Organization: taylor-lab
variant-annotation,VCF annotation utilities
User: tfrayner
variant-annotation,COVID-19 Variants Repository
User: vinodscaria
Home Page: http://vinodscaria.rnabiology.org/covid-19
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