Empirical Bayes somatic variant calling
-
Updated
Oct 25, 2019 - Python
Empirical Bayes somatic variant calling
Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing
Detect and visualize target mutations by scanning FastQ files directly
PhylogicNDT dockcer for clonal evolution analysis
Generate duplex/single consensus reads to reduce sequencing noises and remove duplications
Nextflow bioinformatics pipeline for large-scale analysis of Multiple Myeloma genomes
Assortment of VCF processing scripts
Personal Cancer Genome Reporter (PCGR)
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
Add a description, image, and links to the somatic topic page so that developers can more easily learn about it.
To associate your repository with the somatic topic, visit your repo's landing page and select "manage topics."