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Broad Institute of MIT and Harvard
- Boston, MA
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broadinstitute/infercnv
broadinstitute/infercnv PublicInferring CNV from Single-Cell RNA-Seq
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CTAT-VirusIntegrationFinder
CTAT-VirusIntegrationFinder PublicForked from broadinstitute/CTAT-VirusIntegrationFinder
Python
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NCIP/ctat-mutations
NCIP/ctat-mutations PublicMutation detection using GATK4 best practices and latest RNA editing filters resources. Works with both Hg38 and Hg19
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broadinstitute/infercnvApp
broadinstitute/infercnvApp PublicThis is an R shiny app created as a user friendly way to run the R package infercnv. Infercnv is used to explore tumor single cell RNA-Seq data to identify evidence for somatic large-scale chromoso…
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broadinstitute/infercnvNGCHM
broadinstitute/infercnvNGCHM PublicinferCNV interface to using NGCHM next generation heat maps
R 3
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