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Comprehensive identification of somatic mutations in chronic lymphocytic leukemia
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 hemat...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3145202/ https://ncbi.nlm.nih.gov/pubmed/21741593 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ccr.2011.06.023 |
| Etiketak: |
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