| Literature DB >> 32913073 |
Nicole M Ferraro1, Benjamin J Strober2, Pejman Mohammadi3,4,5, Stephen B Montgomery6,7, Alexis Battle8,9, Jonah Einson10,11, Nathan S Abell12, Francois Aguet13, Alvaro N Barbeira14, Margot Brandt11,15, Maja Bucan16, Stephane E Castel11,15, Joe R Davis7, Emily Greenwald12, Gaelen T Hess12, Austin T Hilliard17, Rachel L Kember16, Bence Kotis4, YoSon Park18, Gina Peloso19, Shweta Ramdas16, Alexandra J Scott20, Craig Smail1, Emily K Tsang7, Seyedeh M Zekavat21, Marcello Ziosi11, Kristin G Ardlie13, Themistocles L Assimes17,22, Michael C Bassik12, Christopher D Brown16, Adolfo Correa23, Ira Hall20, Hae Kyung Im14, Xin Li7,24, Pradeep Natarajan25,26,27, Tuuli Lappalainen11,15.
Abstract
Rare genetic variants are abundant across the human genome, and identifying their function and phenotypic impact is a major challenge. Measuring aberrant gene expression has aided in identifying functional, large-effect rare variants (RVs). Here, we expanded detection of genetically driven transcriptome abnormalities by analyzing gene expression, allele-specific expression, and alternative splicing from multitissue RNA-sequencing data, and demonstrate that each signal informs unique classes of RVs. We developed Watershed, a probabilistic model that integrates multiple genomic and transcriptomic signals to predict variant function, validated these predictions in additional cohorts and through experimental assays, and used them to assess RVs in the UK Biobank, the Million Veterans Program, and the Jackson Heart Study. Our results link thousands of RVs to diverse molecular effects and provide evidence to associate RVs affecting the transcriptome with human traits.Entities:
Mesh:
Year: 2020 PMID: 32913073 PMCID: PMC7646251 DOI: 10.1126/science.aaz5900
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 63.714