Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
A repo that contains miscellaneous Python/C++ modules/programs, a standalone Python module 'palos' by the yfish group (can be installed by pip).
Python toolkit for parsing, processing, and analysis of Illumina methylation array IDAT files
Simulator of SNVs and CNAs in single-cell DNA sequencing
Within-sample CNV calling
A module that parses different diagnostic variant data.
Accurate integration of single-cell DNA and RNA data for a deeper understanding of tumor heterogeneity
