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.
Neighborhood-Aware Variant Impact Predictor
A modular annotation tool for genomic variants
Pipeline for variant annotation using Variant Effect Predictor (VEP)
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