Skip to main content
. 2013 Apr 15;31(15):1825–1833. doi: 10.1200/JCO.2013.48.7215

Fig 2.

Fig 2.

A representative set of tools for the analysis and interpretation of genome sequencing data. These include (A) a listing of representative algorithms for sequencing alignment, (B) variant identification, (C) variant annotation, and (D) clinical interpretation. Boldfaced entries are those specifically geared toward tumor versus normal analysis.

HHS Vulnerability Disclosure