Skip to content

seandavi/CompleteGenomicsTools

Repository files navigation

Overview

Complete Genomics provides whole-genome sequencing using DNA nanoball arrayed sequencing. They also do a relatively thorough job of primary data analysis, but this analysis focuses on single individuals. Often, particularly with cancer genomes, there is a need for further analysis such as comparing tumor versus normal or assessing the sharing of variants across samples.

About

Software for manipulating and visualizing Complete Genomics data, with a focus on cancer

Resources

Stars

Watchers

Forks

Releases

No releases published

Packages

No packages published

Languages