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cnvCurator: an interactive visualization and editing tool for somatic copy number variations
BACKGROUND: One of the most important somatic aberrations, copy number variations (CNVs) in tumor genomes is believed to have a high probability of harboring oncotargets. Detection of somatic CNVs is an essential part of cancer genome sequencing analysis, but the accuracy is usually limited due to v...
Tallennettuna:
| Julkaisussa: | BMC Bioinformatics |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4608136/ https://ncbi.nlm.nih.gov/pubmed/26472134 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0766-y |
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