Identification of novel mutations by exome sequencing in African American colorectal cancer patients

BACKGROUND: To identify genome wide single nucleotide variants (SNVs) and mutations in African Americans (AAs) with colorectal cancer (CRC). There is a need of such studies in AAs since they display a higher incidence of aggressive CRC tumors. METHODS: We performed whole exome sequencing (WES) on DN...

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Gepubliceerd in:Cancer
Hoofdauteurs: Ashktorab, Hassan, Daremipouran, Mohammad, Devaney, Joe, Varma, Sudhir, Rahi, Hamed, Lee, Edward, Shokrani, Babak, Schwartz, Russell, Nickerson, Mike, Brim, Hassan
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: 2014
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4296906/
https://ncbi.nlm.nih.gov/pubmed/25250560
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cncr.28922
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