Literature DB >> 29319195

Strategies for phasing and imputation in a population isolate.

Anthony Francis Herzig1,2, Teresa Nutile3, Marie-Claude Babron1,2, Marina Ciullo3,4, Céline Bellenguez5,6,7, Anne-Louise Leutenegger1,2.   

Abstract

In the search for genetic associations with complex traits, population isolates offer the advantage of reduced genetic and environmental heterogeneity. In addition, cost-efficient next-generation association approaches have been proposed in these populations where only a subsample of representative individuals is sequenced and then genotypes are imputed into the rest of the population. Gene mapping in such populations thus requires high-quality genetic imputation and preliminary phasing. To identify an effective study design, we compare by simulation a range of phasing and imputation software and strategies. We simulated 1,115,604 variants on chromosome 10 for 477 members of the large complex pedigree of Campora, a village within the established isolate of Cilento in southern Italy. We assessed the phasing performance of identical by descent based software ALPHAPHASE and SLRP, LD-based software SHAPEIT2, SHAPEIT3, and BEAGLE, and new software EAGLE that combines both methodologies. For imputation we compared IMPUTE2, IMPUTE4, MINIMAC3, BEAGLE, and new software PBWT. Genotyping errors and missing genotypes were simulated to observe their effects on the performance of each software. Highly accurate phased data were achieved by all software with SHAPEIT2, SHAPEIT3, and EAGLE2 providing the most accurate results. MINIMAC3, IMPUTE4, and IMPUTE2 all performed strongly as imputation software and our study highlights the considerable gain in imputation accuracy provided by a genome sequenced reference panel specific to the population isolate.
© 2018 WILEY PERIODICALS, INC.

Keywords:  founder effect; genotyping errors; identity by descent; linkage disequilibrium; study specific panel

Mesh:

Year:  2018        PMID: 29319195     DOI: 10.1002/gepi.22109

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  9 in total

1.  Kinpute: using identity by descent to improve genotype imputation.

Authors:  Mark Abney; Aisha ElSherbiny
Journal:  Bioinformatics       Date:  2019-11-01       Impact factor: 6.937

2.  Moment estimators of relatedness from low-depth whole-genome sequencing data.

Authors:  Anthony F Herzig; M Ciullo; A-L Leutenegger; H Perdry
Journal:  BMC Bioinformatics       Date:  2022-06-24       Impact factor: 3.307

3.  A comparative analysis of current phasing and imputation software.

Authors:  Adriano De Marino; Abdallah Amr Mahmoud; Madhuchanda Bose; Karatuğ Ozan Bircan; Andrew Terpolovsky; Varuna Bamunusinghe; Sandra Bohn; Umar Khan; Biljana Novković; Puya G Yazdi
Journal:  PLoS One       Date:  2022-10-19       Impact factor: 3.752

4.  Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees.

Authors:  Ehsan Ullah; Raghvendra Mall; Mostafa M Abbas; Khalid Kunji; Alejandro Q Nato; Halima Bensmail; Ellen M Wijsman; Mohamad Saad
Journal:  Genome Res       Date:  2018-12-04       Impact factor: 9.043

5.  Detecting the dominance component of heritability in isolated and outbred human populations.

Authors:  Anthony F Herzig; Teresa Nutile; Daniela Ruggiero; Marina Ciullo; Hervé Perdry; Anne-Louise Leutenegger
Journal:  Sci Rep       Date:  2018-12-21       Impact factor: 4.379

6.  Rare Variants Imputation in Admixed Populations: Comparison Across Reference Panels and Bioinformatics Tools.

Authors:  Sanjeev Sariya; Joseph H Lee; Richard Mayeux; Badri N Vardarajan; Dolly Reyes-Dumeyer; Jennifer J Manly; Adam M Brickman; Rafael Lantigua; Martin Medrano; Ivonne Z Jimenez-Velazquez; Giuseppe Tosto
Journal:  Front Genet       Date:  2019-04-03       Impact factor: 4.599

7.  Very low-depth whole-genome sequencing in complex trait association studies.

Authors:  Arthur Gilly; Lorraine Southam; Daniel Suveges; Karoline Kuchenbaecker; Rachel Moore; Giorgio E M Melloni; Konstantinos Hatzikotoulas; Aliki-Eleni Farmaki; Graham Ritchie; Jeremy Schwartzentruber; Petr Danecek; Britt Kilian; Martin O Pollard; Xiangyu Ge; Emmanouil Tsafantakis; George Dedoussis; Eleftheria Zeggini
Journal:  Bioinformatics       Date:  2019-08-01       Impact factor: 6.937

Review 8.  Hearing loss and tinnitus: association studies for complex-hearing disorders in mouse and man.

Authors:  Ely Cheikh Boussaty; Rick Adam Friedman; Royce E Clifford
Journal:  Hum Genet       Date:  2021-07-27       Impact factor: 5.881

9.  Exploring effective approaches for haplotype block phasing.

Authors:  Ziad Al Bkhetan; Justin Zobel; Adam Kowalczyk; Karin Verspoor; Benjamin Goudey
Journal:  BMC Bioinformatics       Date:  2019-10-30       Impact factor: 3.169

  9 in total

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