Literature DB >> 23756893

Genome-wide complex trait analysis (GCTA): methods, data analyses, and interpretations.

Jian Yang1, Sang Hong Lee, Michael E Goddard, Peter M Visscher.   

Abstract

Estimating genetic variance is traditionally performed using pedigree analysis. Using high-throughput DNA marker data measured across the entire genome it is now possible to estimate and partition genetic variation from population samples. In this chapter, we introduce methods and a software tool called Genome-wide Complex Trait Analysis (GCTA) to estimate genomic relationships between pairs of conventionally unrelated individuals using genome-wide single nucleotide polymorphism (SNP) data, to estimate variance explained by all SNPs simultaneously on genomic or chromosomal segments or over the whole genome, and to perform a joint and conditional multiple SNPs association analysis using summary statistics from a meta-analysis of genome-wide association studies and linkage disequilibrium between SNPs estimated from a reference sample.

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Year:  2013        PMID: 23756893     DOI: 10.1007/978-1-62703-447-0_9

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  77 in total

1.  Leveraging Multi-ethnic Evidence for Mapping Complex Traits in Minority Populations: An Empirical Bayes Approach.

Authors:  Marc A Coram; Sophie I Candille; Qing Duan; Kei Hang K Chan; Yun Li; Charles Kooperberg; Alex P Reiner; Hua Tang
Journal:  Am J Hum Genet       Date:  2015-04-16       Impact factor: 11.025

2.  Cross-tissue and tissue-specific eQTLs: partitioning the heritability of a complex trait.

Authors:  Jason M Torres; Eric R Gamazon; Esteban J Parra; Jennifer E Below; Adan Valladares-Salgado; Niels Wacher; Miguel Cruz; Craig L Hanis; Nancy J Cox
Journal:  Am J Hum Genet       Date:  2014-10-30       Impact factor: 11.025

3.  Characterization of DSM-IV Opioid Dependence Among Individuals of European Ancestry.

Authors:  Leslie A Brick; Lauren Micalizzi; Valerie S Knopik; Rohan H C Palmer
Journal:  J Stud Alcohol Drugs       Date:  2019-05       Impact factor: 2.582

4.  Conditional eQTL analysis reveals allelic heterogeneity of gene expression.

Authors:  Rick Jansen; Jouke-Jan Hottenga; Michel G Nivard; Abdel Abdellaoui; Bram Laport; Eco J de Geus; Fred A Wright; Brenda W J H Penninx; Dorret I Boomsma
Journal:  Hum Mol Genet       Date:  2017-04-15       Impact factor: 6.150

5.  Overlapping genetic effects between suicidal ideation and neurocognitive functioning.

Authors:  Leslie A Brick; Marisa E Marraccini; Lauren Micalizzi; Chelsie E Benca-Bachman; Valerie S Knopik; Rohan H C Palmer
Journal:  J Affect Disord       Date:  2019-02-06       Impact factor: 4.839

6.  Shared additive genetic variation for alcohol dependence among subjects of African and European ancestry.

Authors:  Leslie A Brick; Matthew C Keller; Valerie S Knopik; John E McGeary; Rohan H C Palmer
Journal:  Addict Biol       Date:  2017-11-27       Impact factor: 4.280

7.  Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.

Authors:  Margaux F Keller; Luigi Ferrucci; Andrew B Singleton; Pentti J Tienari; Hannu Laaksovirta; Gabriella Restagno; Adriano Chiò; Bryan J Traynor; Michael A Nalls
Journal:  JAMA Neurol       Date:  2014-09       Impact factor: 18.302

Review 8.  Genetic psychophysiology: advances, problems, and future directions.

Authors:  Andrey P Anokhin
Journal:  Int J Psychophysiol       Date:  2014-04-13       Impact factor: 2.997

9.  Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.

Authors:  Jianjun Gao; Lea K Davis; Amy B Hart; Sandra Sanchez-Roige; Lide Han; John T Cacioppo; Abraham A Palmer
Journal:  Neuropsychopharmacology       Date:  2016-09-15       Impact factor: 7.853

10.  Polygenic Risk of Spasmodic Dysphonia is Associated With Vulnerable Sensorimotor Connectivity.

Authors:  Gregory Garbès Putzel; Giovanni Battistella; Anna F Rumbach; Laurie J Ozelius; Mert R Sabuncu; Kristina Simonyan
Journal:  Cereb Cortex       Date:  2018-01-01       Impact factor: 5.357

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