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Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms
Perl 357 212
Algorithm to implement Fraction and Copy number Estimate from Tumor/normal Sequencing.
R 134 65
Filters for false-positive mutation calls in NGS
R 30 21
Forked from rhshah/iCallSV
A Framework to call Structural Variants from NGS based datasets
Python 3 1
Create mutation signatures from MAF's, and decompose them into Stratton signatures
R 59 30
Runs all thenextflow workflow scripts for IMPACT processing
Nextflow workflow for handling Structural Variants
Sample QC with nodejs backend
Repository for ARGOS report (v1.0.1 Balto)
Toil API
Voyager Backend
Demultiplex Illumina sequencer output via DRAGEN, create fastq files and launch pipelines
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