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Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X
We developed cis-X, a computational method for discovery of regulatory noncoding variants in cancer by integrating whole genome and transcriptome sequencing data from a single cancer sample. cis-X first finds aberrantly cis-activated genes that exhibit allele-specific expression accompanied by an el...
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| 出版年: | Nat Genet |
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| 主要な著者: | , , , , , , , , , , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2020
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7679232/ https://ncbi.nlm.nih.gov/pubmed/32632335 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41588-020-0659-5 |
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