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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Lingfei, Michoel, Tom
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576763/
https://www.ncbi.nlm.nih.gov/pubmed/28821014
http://dx.doi.org/10.1371/journal.pcbi.1005703

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576763/
https://www.ncbi.nlm.nih.gov/pubmed/28821014
http://dx.doi.org/10.1371/journal.pcbi.1005703

Ejemplares similares