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Calling genotypes from public RNA-sequencing data enables identification of genetic variants that affect gene-expression levels
BACKGROUND: RNA-sequencing (RNA-seq) is a powerful technique for the identification of genetic variants that affect gene-expression levels, either through expression quantitative trait locus (eQTL) mapping or through allele-specific expression (ASE) analysis. Given increasing numbers of RNA-seq samp...
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| 出版年: | Genome Med |
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| 主要な著者: | , , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2015
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4423486/ https://ncbi.nlm.nih.gov/pubmed/25954321 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-015-0152-4 |
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