Načítá se...
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...
Uloženo v:
| Vydáno v: | PLoS Comput Biol |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2017
|
| Témata: | |
| On-line přístup: | 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 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|