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VizCNV
VizCNV PublicForked from cluhaowie/VizCNV
VizCNV is an interactive tool designed to analyze and visualize CNVs from short read WGS data in rare disease research. Built on R Studio Shiny, it streamlines the identification of complex genomic…
R
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RepeatPhaserMethPipeline
RepeatPhaserMethPipeline PublicA Python pipeline to phase long-read sequencing data using tandem repeat polymorphisms, tag reads by haplotype, and perform downstream methylation analysis to assess allelic imbalance and X-inactiv…
Python
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CLDB
CLDB PublicForked from clifflun/CLDB
CLDB is a Python-based toolkit designed to support flexible management and querying of copy-number variant (CNV) / structural variant (SV) metadata for genomic analyses
Python
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