Research

Robust analysis of allele-specific copy number alterations from scRNA-seq data with XClone

XClone is an algorithm to infer allele- and haplotype-specific copy numbers in individual cells from low-coverage and sparse single-cell RNA sequencing data (e.g., those generated by 10x Genomics, Smart-seq, etc.)

RPG seminar: XClone

XClone

MQuad enables clonal substructure discovery using single cell mitochondrial variants

MQuad: Mixture Model for Mitochondrial Mutation detection in single-cell omics data

Report_PTM-X_inter

PTM-X

Systematic characterization and prediction of post-translational modification cross-talk between proteins

A valuable tool to identify inter-protein PTM cross-talk at proteome-wide scale.