PPT-Rare and common variants: twenty arguments
Author : pasty-toler | Published Date : 2015-11-18
GGibson Homework 3 Mylène Champs Marine Flechet Mathieu Stifkens 1 Bioinformatics GBIO00091 KVan Steen University of
Presentation Embed Code
Download Presentation
Download Presentation The PPT/PDF document "Rare and common variants: twenty argumen..." is the property of its rightful owner. Permission is granted to download and print the materials on this website for personal, non-commercial use only, and to display it on your personal computer provided you do not modify the materials and that you retain all copyright notices contained in the materials. By downloading content from our website, you accept the terms of this agreement.
Rare and common variants: twenty arguments: Transcript
GGibson Homework 3 Mylène Champs Marine Flechet Mathieu Stifkens 1 Bioinformatics GBIO00091 KVan Steen University of . 6 December 2012. Introduction. I. mputation describes the process of predicting genotypes that have not been directly typed in a sample of individuals:. m. issing genotypes at typed variants;. genotypes at un-typed variants that are present in an external high-density “reference panel” of phased . Gil . McVean. There are no new questions in population genetics. …only new types of data. Genome sequences of entire populations. Data with linkage to deep phenotype information. Data from multiple species. Lipika. Ray. 4th . June 2010. Heritability:. Phenotype (P) = genotype (G) + environmental factors (E). (observed) (unobserved) (unobserved). Variances:. Heritability is defined as ratio of variances, by expressing the proportion of the phenotypic variance that can be attributed to variance of genotypic values:. Andrew Morris. Advanced Topics in GWAS. Toronto, 30 May 2012. Introduction. GWAS have been successful in detecting . novel loci for complex traits:. typically characterised by common variants of modest effect;. sibpair. test for rare variant . association. Sebastian Zöllner. University of Michigan. . . . Acknowledgements. Matthew . Zawistowski. Keng. -Han Lin. Mark . Reppell. Biases, confounding factors, current methods, and best practices. Luke Evans, Matthew Keller. Background – What Matt Keller presented. GREML-SC: single genetic relatedness matrix (GRM) to estimate heritability (. Professor . Department of . Epidemiology and. Genetic Epidemiology Research Institute. University . of . California, Irvine. . Irvine, CA. kedward1@uci.edu. What is old is new. Rare Variants. This session. Implications for . Germline. Editing. Human Diseases and Traits. Rare, . Mendelian. Cystic fibrosis, . Huntington Disease,. Diastrophic Dysplasia . …. Common, . polygenic. Heart disease, Alzheimer’s. .Wild BergamotMonarda fistulosaR - rare (1-10/acre)Plantawaste.CatnipNepeta catariaR - rare (1-10/acre)Compsandy prairie 10Scribner's Panic GrassPanicum oligosanthes scribneriaR - rare (1-10/acre)Cype Michael Adams. 1. , James Evans. 1. , Gail Henderson. 2. , Jonathan S. Berg. 1. . 1. Department of Genetics, UNC-Chapel . Hill 2. . . Department of Social Medicine, UNC-Chapel Hill. Introduction. Genomic screening of the general population for preventable, monogenic disease has potential to decrease morbidity and . as guides to pain mechanisms . and drug development. Alban Latremoliere, Ph.D. .. ACCELERATING THE DEVELOPMENT OF PRECISION PAIN MEDICINE, IMMPACT XIX. Friday, June 3rd, 2016 . Kirby Neurobiology Center. heritability. (“GWAS and heritability”). peter.visscher@uq.edu.au. 1. The original definition of ‘missing heritability’. NB both are estimates that can be biased (up or down). . 2. My 2009 presentation. cold, and gastrointestinal (GI) illness ahs.ca/covid COVID-19 Inuenza (Flu) Cold GI Illness (Stomach Flu) Caused by SARS-CoV-2 virus Inuenza A or Inuenza B viruses Many As an alternative, Speakman has putforward a non-adaptive scenariothe drifty gene hypothesis.According to this idea, genetic drift the change ofgenefrequencies due to random, non-selective proce
Download Document
Here is the link to download the presentation.
"Rare and common variants: twenty arguments"The content belongs to its owner. You may download and print it for personal use, without modification, and keep all copyright notices. By downloading, you agree to these terms.
Related Documents