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Targeted deep resequencing of the human cancer genome using next-generation technologies
Next generation sequencing technologies have revolutionized our ability to identify genetic variants, either germline or somatic point mutations, that occur in cancer. Parallelization and miniaturization of DNA sequencing enables massive data throughput and for the first time, large-scale, base pair...
Gorde:
| Argitaratua izan da: | Biotechnol Genet Eng Rev |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2010
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4340661/ https://ncbi.nlm.nih.gov/pubmed/21415896 |
| Etiketak: |
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