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Assessing Matched Normal and Tumor Pairs in Next-Generation Sequencing Studies
Next generation sequencing technology has revolutionized the study of cancers. Through matched normal-tumor pairs, it is now possible to identify genome-wide germline and somatic mutations. The generation and analysis of the data requires rigorous quality checks and filtering, and the current analyt...
Tallennettuna:
| Päätekijät: | , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3060821/ https://ncbi.nlm.nih.gov/pubmed/21445261 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0017810 |
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