Pinned Repositories
EBCall
an empirical Bayesian framework for mutation detection from cancer genome sequencing data
cnvkit
Copy number variant detection from targeted DNA sequencing
deepvariant
DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
facets
Algorithm to implement Fraction and Copy number Estimate from Tumor/normal Sequencing.
igv
Integrative Genomics Viewer. Fast, efficient, scalable visualization tool for genomics data and annotations
RSeQC
fork of RSeQC python RNAseq metrics suit of tools
STAR-Fusion
STAR-Fusion codebase
VarDict
VarDict
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