| Literature DB >> 21741593 |
P Leif Bergsagel1, W Michael Kuehl.
Abstract
Massively parallel sequencing enables the sequencing of whole genomes, exomes, and transcriptomes from many tumor samples. Thus, it now is possible to comprehensively identify somatic mutations, including single base changes, deletions, insertions, and genomic rearrangements. Early results for hematopoietic tumors show great promise, but many questions remain to be answered.Entities:
Year: 2011 PMID: 21741593 PMCID: PMC3145202 DOI: 10.1016/j.ccr.2011.06.023
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743