BEGIN:VCALENDAR VERSION:2.0 PRODID:-//132.216.98.100//NONSGML kigkonsult.se iCalcreator 2.20.4// BEGIN:VEVENT UID:20250808T192816EDT-14216RMtPS@132.216.98.100 DTSTAMP:20250808T232816Z DESCRIPTION:\n Title: What is TWAS and how do we use it in integrating gene expression data\n\n Abstract:\n\n\nThe transcriptome-wide association studi es (TWAS) is a pioneering approach utilizing gene expression data to ident ify genetic basis of complex diseases. Its core component is called “genet ically regulated expression (GReX)”. GReX links gene expression informatio n with phenotype by serving as both the outcome of genotype-based expressi on models and the predictor for downstream association testing. Although i t is popular and has been used in many high-profile projects\, its mathema tical nature and interpretation haven’t been rigorously verified. As such\ , we have first conducted power analysis using NCP-based closed forms (Cao et al\, PLoS Genet 2021)\, based on which we realized that the common int erpretation of TWAS that looks biologically sensible is actually mathemati cally questionable. Following this insight\, by real data analysis and sim ulations\, we demonstrated that current linear models of GReX inadvertentl y combine two separable steps of machine learning - feature selection and aggregation - which can be independently replaced to improve overall power (Cao et al\, Genetics 2021). Based on this new interpretation\, we have d eveloped novel protocols disentangling feature selections and aggregations \, leading to improved power and novel biological discoveries (Cao et al\, BiB 2021\; Genetics 2021). To promote this new understanding\, we moved f orward to develop two statistical tools utilizing gene expressions in iden tifying genetic basis of gene-gene interactions (Kossinna et al\, in prepa ration) and low-effect genetic variants (Li et al\, in review)\, respectiv ely. Looking forward\, our mathematical characterization of TWAS opens a d oor for a new way to integrate gene expressions in genetic studies towards the realization of precision medicine.\n\n\n Speaker\n\n\nQuan Long is an Associate Professor at University of Calgary\, hosted by the Dept. of Bioc hemistry and Molecular Biology. He has a joint appointment in the Dept. of Medical Genetics and an adjunct appointment in the Dept. of Math and Stat s. He is a member of Alberta Children’s Hospital Research Institute and Ho tchkiss Brain Institute. Currently he is leading a research group to devel op computational and statistical tools\, focusing on genomic problems with high-dimensional features and low sample sizes. He is also interested in theoretical problems in machine learning.\n\nhttps://mcgill.zoom.us/j/8343 6686293?pwd=b0RmWmlXRXE3OWR6NlNIcWF5d0dJQT09\n\nMeeting ID: 834 3668 6293 \n\nPasscode: 12345\n\n \n\n \n DTSTART:20230120T203000Z DTEND:20230120T213000Z SUMMARY:Quan Long (University of Calgary) URL:/mathstat/channels/event/quan-long-university-calg ary-345120 END:VEVENT END:VCALENDAR