anbianchi/IntegratedSNVINDELSandCNV
An adaptable method for analyzing SNVs, INDELs, and CNVs from Whole Exome Sequencing (WES) data, emphasizing germline variants.
PythonMIT
No issues in this repository yet.
An adaptable method for analyzing SNVs, INDELs, and CNVs from Whole Exome Sequencing (WES) data, emphasizing germline variants.
PythonMIT
No issues in this repository yet.