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Convert a VCF into a MAF, where each variant is annotated to only one of all possible gene isoforms
Perl 373 216
Algorithm to implement Fraction and Copy number Estimate from Tumor/normal Sequencing.
R 140 67
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 60 30
CCS research pipeline to process WES and WGS TN pairs
ecDNA detection pipeline for MSK Sequencing Data
Voyager Backend
Pipeline for computing neoantigen qualities from DNA and RNA-Seq data
NGS Statistics Database with historical Picard Stats, IGO fastq.gz paths and Sequencer Start & Stop Times
Load, review and adjust facets fits
Functional Observation of RNA Transcriptome Elements/Expression
Toil API
Sample Submission API written in node.js
Beagle API Command Line Utility
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