Literature DB >> 24632498

FSuite: exploiting inbreeding in dense SNP chip and exome data.

Steven Gazal1, Mourad Sahbatou2, Marie-Claude Babron1, Emmanuelle Génin1, Anne-Louise Leutenegger1.   

Abstract

UNLABELLED: FSuite is a user-friendly pipeline developed for exploiting inbreeding information derived from human genomic data. It can make use of single nucleotide polymorphism chip or exome data. Compared with other software, the advantage of FSuite is that it provides a complete suite of scripts to describe and use the inbreeding information. It includes a module to detect inbred individuals and estimate their inbreeding coefficient, a module to describe the proportion of different mating types in the population and the individual probability to be offspring of different mating types that can be useful for population genetic studies. It also allows the identification of shared regions of homozygosity between affected individuals (homozygosity mapping) that can be used to identify rare recessive mutations involved in monogenic or multifactorial diseases.
AVAILABILITY AND IMPLEMENTATION: FSuite is developed in Perl and uses R functions to generate graphical outputs. This pipeline is freely available under GNU GPL license at: http://genestat.cephb.fr/software/index.php/FSuite.
© The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

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Year:  2014        PMID: 24632498     DOI: 10.1093/bioinformatics/btu149

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  17 in total

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

Authors:  Steven Gazal; Simon Gosset; Edgard Verdura; Françoise Bergametti; Stéphanie Guey; Marie-Claude Babron; Elisabeth Tournier-Lasserve
Journal:  Eur J Hum Genet       Date:  2015-07-15       Impact factor: 4.246

2.  Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Suriname.

Authors:  Cesar Fortes-Lima; Antoine Gessain; Andres Ruiz-Linares; Maria-Cátira Bortolini; Florence Migot-Nabias; Gil Bellis; J Víctor Moreno-Mayar; Berta Nelly Restrepo; Winston Rojas; Efren Avendaño-Tamayo; Gabriel Bedoya; Ludovic Orlando; Antonio Salas; Agnar Helgason; M Thomas P Gilbert; Martin Sikora; Hannes Schroeder; Jean-Michel Dugoujon
Journal:  Am J Hum Genet       Date:  2017-11-02       Impact factor: 11.025

3.  Mutations in the genes for thyroglobulin and thyroid peroxidase cause thyroid dyshormonogenesis and autosomal-recessive intellectual disability.

Authors:  Kirti Mittal; Muhammad A Rafiq; Rafiullah Rafiullah; Ricardo Harripaul; Hazrat Ali; Muhammad Ayaz; Muhammad Aslam; Farooq Naeem; Muhammad Amin-Ud-Din; Ahmed Waqas; Joyce So; Gudrun A Rappold; John B Vincent; Muhammad Ayub
Journal:  J Hum Genet       Date:  2016-06-16       Impact factor: 3.172

4.  From matrimonial practices to genetic diversity in Southeast Asian populations: the signature of the matrilineal puzzle.

Authors:  Goki Ly; Romain Laurent; Sophie Lafosse; Chou Monidarin; Gérard Diffloth; Frédéric Bourdier; Olivier Evrard; Bruno Toupance; Samuel Pavard; Raphaëlle Chaix
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2019-07-15       Impact factor: 6.237

5.  Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.

Authors:  R Harripaul; N Vasli; A Mikhailov; M A Rafiq; K Mittal; C Windpassinger; T I Sheikh; A Noor; H Mahmood; S Downey; M Johnson; K Vleuten; L Bell; M Ilyas; F S Khan; V Khan; M Moradi; M Ayaz; F Naeem; A Heidari; I Ahmed; S Ghadami; Z Agha; S Zeinali; R Qamar; H Mozhdehipanah; P John; A Mir; M Ansar; L French; M Ayub; J B Vincent
Journal:  Mol Psychiatry       Date:  2017-04-11       Impact factor: 15.992

Review 6.  Using familial information for variant filtering in high-throughput sequencing studies.

Authors:  Melanie Bahlo; Rick Tankard; Vesna Lukic; Karen L Oliver; Katherine R Smith
Journal:  Hum Genet       Date:  2014-08-17       Impact factor: 4.132

7.  Homozygous STIL mutation causes holoprosencephaly and microcephaly in two siblings.

Authors:  Charlotte Mouden; Marie de Tayrac; Christèle Dubourg; Sophie Rose; Wilfrid Carré; Houda Hamdi-Rozé; Marie-Claude Babron; Linda Akloul; Bénédicte Héron-Longe; Sylvie Odent; Valérie Dupé; Régis Giet; Véronique David
Journal:  PLoS One       Date:  2015-02-06       Impact factor: 3.240

8.  High level of inbreeding in final phase of 1000 Genomes Project.

Authors:  Steven Gazal; Mourad Sahbatou; Marie-Claude Babron; Emmanuelle Génin; Anne-Louise Leutenegger
Journal:  Sci Rep       Date:  2015-12-02       Impact factor: 4.379

Review 9.  Genomics advances the study of inbreeding depression in the wild.

Authors:  Marty Kardos; Helen R Taylor; Hans Ellegren; Gordon Luikart; Fred W Allendorf
Journal:  Evol Appl       Date:  2016-10-23       Impact factor: 5.183

10.  Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage.

Authors:  Aziz Belkadi; Vincent Pedergnana; Aurélie Cobat; Yuval Itan; Quentin B Vincent; Avinash Abhyankar; Lei Shang; Jamila El Baghdadi; Aziz Bousfiha; Alexandre Alcais; Bertrand Boisson; Jean-Laurent Casanova; Laurent Abel
Journal:  Proc Natl Acad Sci U S A       Date:  2016-05-31       Impact factor: 11.205

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