| Literature DB >> 33668793 |
Gennady Khvorykh1, Andrey Khrunin1, Ivan Filippenkov1, Vasily Stavchansky1, Lyudmila Dergunova1, Svetlana Limborska1.
Abstract
In this paper we propose a workflow for studying the genetic architecture of ischemic stroke outcomes. It develops further the candidate gene approach. The workflow is based on the animal model of brain ischemia, comparative genomics, human genomic variations, and algorithms of selection of tagging single nucleotide polymorphisms (tagSNPs) in genes which expression was changed after ischemic stroke. The workflow starts from a set of rat genes that changed their expression in response to brain ischemia and results in a set of tagSNPs, which represent other SNPs in the human genes analyzed and influenced on their expression as well.Entities:
Keywords: human orthologues; ischemic stroke; models of brain ischemia; single nucleotide polymorphisms
Year: 2021 PMID: 33668793 PMCID: PMC7996278 DOI: 10.3390/genes12030328
Source DB: PubMed Journal: Genes (Basel) ISSN: 2073-4425 Impact factor: 4.096