Efficient and accurate causal inference with hidden confounders from genome-transcriptome variation data.

Wang, Lingfei; Michoel, Tom

Wang, Lingfei; Michoel, Tom.

Affiliation

Wang L; Division of Genetics and Genomics, The Roslin Institute, The University of Edinburgh, Easter Bush, Midlothian, United Kingdom.
Michoel T; Division of Genetics and Genomics, The Roslin Institute, The University of Edinburgh, Easter Bush, Midlothian, United Kingdom.

PLoS Comput Biol ; 13(8): e1005703, 2017 Aug.

Article in En | MEDLINE | ID: mdl-28821014

Subject(s)

Chromosome Mapping; High-Throughput Nucleotide Sequencing; Transcriptome/genetics; Algorithms; Chromosome Mapping/methods; Chromosome Mapping/standards; Databases, Genetic; Genetic Variation; High-Throughput Nucleotide Sequencing/methods; High-Throughput Nucleotide Sequencing/standards; Models, Statistical

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosome Mapping / High-Throughput Nucleotide Sequencing / Transcriptome Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: PLoS Comput Biol Journal subject: BIOLOGIA / INFORMATICA MEDICA Year: 2017 Type: Article Affiliation country: United kingdom

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