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Detecting large deletions at base pair level by combining split read and paired read data
BACKGROUND: Genomic structural variants (SV) play a significant role in the onset and progression of cancer. Genomic deletions can create oncogenic fusion genes or cause the loss of tumor suppressing gene function which can lead to tumorigenesis by downregulating these genes. Detecting these variant...
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| Publicado no: | BMC Bioinformatics |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5657039/ https://ncbi.nlm.nih.gov/pubmed/29072143 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1829-z |
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