Literature DB >> 25824869

Genetic linkage analysis in the age of whole-genome sequencing.

Jurg Ott1, Jing Wang2, Suzanne M Leal3.   

Abstract

For many years, linkage analysis was the primary tool used for the genetic mapping of Mendelian and complex traits with familial aggregation. Linkage analysis was largely supplanted by the wide adoption of genome-wide association studies (GWASs). However, with the recent increased use of whole-genome sequencing (WGS), linkage analysis is again emerging as an important and powerful analysis method for the identification of genes involved in disease aetiology, often in conjunction with WGS filtering approaches. Here, we review the principles of linkage analysis and provide practical guidelines for carrying out linkage studies using WGS data.

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Year:  2015        PMID: 25824869      PMCID: PMC4440411          DOI: 10.1038/nrg3908

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  92 in total

1.  Linkage disequilibrium and the mapping of complex human traits.

Authors:  Kenneth M Weiss; Andrew G Clark
Journal:  Trends Genet       Date:  2002-01       Impact factor: 11.639

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Authors:  Joan E Bailey-Wilson; Alexander F Wilson
Journal:  Hum Hered       Date:  2011-12-23       Impact factor: 0.444

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Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

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Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

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Journal:  Hum Hered       Date:  1971       Impact factor: 0.444

6.  Molecular and statistical approaches to the detection and correction of errors in genotype databases.

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Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

7.  Detecting marker inconsistencies in human gene mapping.

Authors:  J Ott
Journal:  Hum Hered       Date:  1993 Jan-Feb       Impact factor: 0.444

8.  Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis.

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Journal:  Nat Genet       Date:  1994-12       Impact factor: 38.330

9.  Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish.

Authors:  Regie Lyn P Santos-Cortez; Kwanghyuk Lee; Arnaud P Giese; Muhammad Ansar; Muhammad Amin-Ud-Din; Kira Rehn; Xin Wang; Abdul Aziz; Ilene Chiu; Raja Hussain Ali; Joshua D Smith; Jay Shendure; Michael Bamshad; Deborah A Nickerson; Zubair M Ahmed; Wasim Ahmad; Saima Riazuddin; Suzanne M Leal
Journal:  Hum Mol Genet       Date:  2014-01-29       Impact factor: 6.150

10.  Genetic determinants of diastolic and pulse pressure map to different loci in Lyon hypertensive rats.

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Journal:  Nat Genet       Date:  1993-04       Impact factor: 38.330

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Journal:  Mol Psychiatry       Date:  2016-07-19       Impact factor: 15.992

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4.  Can whole-exome sequencing data be used for linkage analysis?

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5.  Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits.

Authors:  Biao Li; Gao T Wang; Suzanne M Leal
Journal:  Bioinformatics       Date:  2015-07-14       Impact factor: 6.937

6.  A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).

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Journal:  Eur J Hum Genet       Date:  2019-04-11       Impact factor: 4.246

Review 7.  Tea plant genomics: achievements, challenges and perspectives.

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8.  MendelProb: probability and sample size calculations for Mendelian studies of exome and whole genome sequence data.

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9.  Defining human insulin-like growth factor I gene regulation.

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Review 10.  Society for Pediatric Research 2015 Young Investigator Award: genetics of human hematopoiesis-what patients can teach us about blood cell production.

Authors:  Aoi Wakabayashi; Vijay G Sankaran
Journal:  Pediatr Res       Date:  2015-11-17       Impact factor: 3.756

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