Pinned Repositories
awesome-bioinformatics-benchmarks
A curated list of bioinformatics bench-marking papers and resources.
bio-uoc
clear-cnv
ClearCNV - CNV analysis in the presence of ambiguity and noise
CNVbenchmarkeR2
Framework to benchmark germline copy-number variant detection tools from NGS data
CNVfilteR
R package to remove false positives of CNV calling tools by using SNV calls
cnvkit
Copy number variant detection from targeted DNA sequencing
imdb
swampdragon
swampdragon
SigMA
Mutational signature analysis for low statistics SNV data
CNVbenchmarkeR
Framework to benchmark algorithms when detecting germline copy number variations (CNVs) from NGS data
jpuntomarcos's Repositories
jpuntomarcos/CNVfilteR
R package to remove false positives of CNV calling tools by using SNV calls
jpuntomarcos/CNVbenchmarkeR2
Framework to benchmark germline copy-number variant detection tools from NGS data
jpuntomarcos/awesome-bioinformatics-benchmarks
A curated list of bioinformatics bench-marking papers and resources.
jpuntomarcos/bio-uoc
jpuntomarcos/clear-cnv
ClearCNV - CNV analysis in the presence of ambiguity and noise
jpuntomarcos/cnvkit
Copy number variant detection from targeted DNA sequencing
jpuntomarcos/imdb
jpuntomarcos/swampdragon
swampdragon