| Literature DB >> 34260399 |
Darui Xu1, Stephen Lyon1, Chun Hui Bu1, Sara Hildebrand1, Jin Huk Choi1,2, Xue Zhong1, Aijie Liu1, Emre E Turer1,3, Zhao Zhang1, Jamie Russell1, Sara Ludwig1, Elena Mahrt1, Evan Nair-Gill1, Hexin Shi1, Ying Wang1, Duanwu Zhang1, Tao Yue1, Kuan-Wen Wang1, Jeffrey A SoRelle1, Lijing Su1, Takuma Misawa1, William McAlpine1, Lei Sun1, Jianhui Wang1, Xiaoming Zhan1, Mihwa Choi1, Roxana Farokhnia1, Andrew Sakla1, Sara Schneider1, Hannah Coco1, Gabrielle Coolbaugh1, Braden Hayse1, Sara Mazal1, Dawson Medler1, Brandon Nguyen1, Edward Rodriguez1, Andrew Wadley1, Miao Tang1, Xiaohong Li1, Priscilla Anderton1, Katie Keller1, Amanda Press1, Lindsay Scott1, Jiexia Quan1, Sydney Cooper1, Tiffany Collie1, Baifang Qin1, Jennifer Cardin1, Rochelle Simpson1, Meron Tadesse1, Qihua Sun1, Carol A Wise4,5,6,7, Jonathan J Rios4,5,6,7, Eva Marie Y Moresco1, Bruce Beutler8.
Abstract
Forward genetic studies use meiotic mapping to adduce evidence that a particular mutation, normally induced by a germline mutagen, is causative of a particular phenotype. Particularly in small pedigrees, cosegregation of multiple mutations, occasional unawareness of mutations, and paucity of homozygotes may lead to erroneous declarations of cause and effect. We sought to improve the identification of mutations causing immune phenotypes in mice by creating Candidate Explorer (CE), a machine-learning software program that integrates 67 features of genetic mapping data into a single numeric score, mathematically convertible to the probability of verification of any putative mutation-phenotype association. At this time, CE has evaluated putative mutation-phenotype associations arising from screening damaging mutations in ∼55% of mouse genes for effects on flow cytometry measurements of immune cells in the blood. CE has therefore identified more than half of genes within which mutations can be causative of flow cytometric phenovariation in Mus musculus The majority of these genes were not previously known to support immune function or homeostasis. Mouse geneticists will find CE data informative in identifying causative mutations within quantitative trait loci, while clinical geneticists may use CE to help connect causative variants with rare heritable diseases of immunity, even in the absence of linkage information. CE displays integrated mutation, phenotype, and linkage data, and is freely available for query online.Entities:
Keywords: ENU mutagenesis; automated meiotic mapping; flow cytometry; immune cells; machine learning
Mesh:
Year: 2021 PMID: 34260399 PMCID: PMC8285956 DOI: 10.1073/pnas.2106786118
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 12.779