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Published byAsher Arnold Anthony Modified over 5 years ago
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Fig. 1. Schematic description of whole-exome or targeted next-generation sequencing analyses.
Schematic description of whole-exome or targeted next-generation sequencing analyses. The approaches used tumor-only (blue arrow) or matched tumor and normal DNA (red arrow) to identify sequence alterations. Bioinformatic methods to separate germline and somatic changes included comparison to dbSNP, COSMIC, and kinase domain databases. Identified gene alterations were compared to databases of established and experimental therapies to identify potential clinical actionability and predisposing alterations. Siân Jones et al., Sci Transl Med 2015;7:283ra53 Copyright © 2015, American Association for the Advancement of Science
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