Containerized workflow for analysis of human diabetic kidney disease by snRNA-seq and snATAC-seq
Algorithm to implement Fraction and Allelic Copy number Estimate from Tumor/normal Sequencing using unmatched normal sample(s) for log ratio calculations
Analysis scripts for the Vertesy 2018 paper: "Parental haplotype specific single-cell transcriptomics reveal incomplete epigenetic reprogramming in human female germ cells"
R scripts to process input/output related to GeneiASE software
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