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CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing
Germline copy number variants (CNVs) and somatic copy number alterations (SCNAs) are of significant importance in syndromic conditions and cancer. Massively parallel sequencing is increasingly used to infer copy number information from variations in the read depth in sequencing data. However, this a...
Tallennettuna:
| Julkaisussa: | PLoS Comput Biol |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4839673/ https://ncbi.nlm.nih.gov/pubmed/27100738 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1004873 |
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