A flexible variant annotator written in Python
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Updated
Jul 11, 2017
A flexible variant annotator written in Python
2019 Genomics Epidemiology Workshop at Academia Sinica
OpenCRAVAT as a GenePattern module
COVID-19 Variants Repository
A python parser to simplify and build the VCF (Variant Call Format).
A tool for analysis of genomic variants in human genomes.
A tool for prioritising identity-by-descent (IBD) variants in Whole Genome Sequencing (WGS) data from families with rare heritable diseases.
Automated statistical and functional fine-mapping pipeline with extensive API access to datasets.
Add functional variant annotation to MAF file
💻 Command line interface for Genome Nexus 🧬
The DKFZ-ODCF, formerly DKFZ/eilslabs SNV-Calling Workflow
Annotate genomics variations of hg19 by using a BED format database, which construct from NCBI annotation release 104
Library for indexing VCF files for random access searches by rsID
Human mitochondrial variants annotation using HmtVar.
Analysis pipleine to model tumour clonal evolution from WGS data (driver annotation, quality control of copy number calls, subclonal and mutational signature deconvolution)
Neighborhood-Aware Variant Impact Predictor
Variant Calling and Annotation using PacBio Hi-Fi Reads
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