Read mismapping from segmental duplications drives spurious trans associations

片段重复导致的读取错误映射会造成虚假的跨基因关联。

阅读:1

Abstract

Heritable variation in gene regulation shapes both disease risk and evolution. Trans-acting quantitative trait loci (trans-QTLs) are the primary source of this variation within species, but they remain difficult to identify correctly due to false positives stemming from RNA and DNA read mismapping. Here, we identify four categories of RNA and DNA mismapping due to segmental duplications that lead to false-positive trans-QTLs. Such mismapping leaves a footprint in the form of long-range genotypic disequilibrium, which we use to identify spurious trans-QTLs. Applying this method to Genotype-Tissue Expression (GTEx) trans-QTL, we conservatively estimate that 14% of expression QTLs, 10% of splicing QTLs, and 3% of protein QTLs are artifacts. More broadly, this framework could be applied to flag spurious distant peaks in genome-wide association studies, Hi-C contacts, and co-expression between distant genes.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。