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A fast detection of fusion genes from paired-end RNA-seq data
BACKGROUND: Fusion genes are known to be drivers of many common cancers, so they are potential markers for diagnosis, prognosis or therapy response. The advent of paired-end RNA sequencing enhances our ability to discover fusion genes. While there are available methods, routine analyses of large num...
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| 發表在: | BMC Genomics |
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| Main Authors: | , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2018
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6211471/ https://ncbi.nlm.nih.gov/pubmed/30382840 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-018-5156-1 |
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