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Efficient and accurate causal inference with hidden confounders from genome-transcriptome variation data
Mapping gene expression as a quantitative trait using whole genome-sequencing and transcriptome analysis allows to discover the functional consequences of genetic variation. We developed a novel method and ultra-fast software Findr for higly accurate causal inference between gene expression traits u...
Gorde:
| Argitaratua izan da: | PLoS Comput Biol |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Public Library of Science
2017
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5576763/ https://ncbi.nlm.nih.gov/pubmed/28821014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1005703 |
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