Recombination networks as genetic markers in a human variation study of the Old World

We have analyzed human genetic diversity in 33 Old World populations including 23 populations obtained through Genographic Project studies. A set of 1,536 SNPs in five X chromosome regions were genotyped in 1,288 individuals (mostly males). We use a novel analysis employing subARG network constructi...

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Main Author: Javed, Asif (author)
Other Authors: Mele, Marta (author), Pybus, Marc (author), Zalloua, Pierre (author), Haber, Marc (author), Comas, David (author), Netea, Mihai G. (author), Balanovsky, Oleg (author), Balanovsky, Elena (author), Jin, Li (author), Yang, Yajun (author), ArunKumar, GaneshPrasad (author), Pitchappan, Ramasamy (author), Bertranpetit, Jaume (author), Calafell, Francesc (author)
Format: article
Published: 2012
Online Access:http://hdl.handle.net/10725/11118
https://doi.org/10.1007/s00439-011-1104-8
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://link.springer.com/article/10.1007/s00439-011-1104-8
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author Javed, Asif
author2 Mele, Marta
Pybus, Marc
Zalloua, Pierre
Haber, Marc
Comas, David
Netea, Mihai G.
Balanovsky, Oleg
Balanovsky, Elena
Jin, Li
Yang, Yajun
ArunKumar, GaneshPrasad
Pitchappan, Ramasamy
Bertranpetit, Jaume
Calafell, Francesc
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author_facet Javed, Asif
Mele, Marta
Pybus, Marc
Zalloua, Pierre
Haber, Marc
Comas, David
Netea, Mihai G.
Balanovsky, Oleg
Balanovsky, Elena
Jin, Li
Yang, Yajun
ArunKumar, GaneshPrasad
Pitchappan, Ramasamy
Bertranpetit, Jaume
Calafell, Francesc
author_role author
dc.creator.none.fl_str_mv Javed, Asif
Mele, Marta
Pybus, Marc
Zalloua, Pierre
Haber, Marc
Comas, David
Netea, Mihai G.
Balanovsky, Oleg
Balanovsky, Elena
Jin, Li
Yang, Yajun
ArunKumar, GaneshPrasad
Pitchappan, Ramasamy
Bertranpetit, Jaume
Calafell, Francesc
dc.date.none.fl_str_mv 2012
2019-07-22T08:02:46Z
2019-07-22T08:02:46Z
2019-07-22
dc.identifier.none.fl_str_mv 1432-1203
http://hdl.handle.net/10725/11118
https://doi.org/10.1007/s00439-011-1104-8
Javed, A., Melé, M., Pybus, M., Zalloua, P., Haber, M., Comas, D., ... & Yang, Y. (2012). Recombination networks as genetic markers in a human variation study of the Old World. Human genetics, 131(4), 601-613.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://link.springer.com/article/10.1007/s00439-011-1104-8
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Human Genetics
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Recombination networks as genetic markers in a human variation study of the Old World
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description We have analyzed human genetic diversity in 33 Old World populations including 23 populations obtained through Genographic Project studies. A set of 1,536 SNPs in five X chromosome regions were genotyped in 1,288 individuals (mostly males). We use a novel analysis employing subARG network construction with recombining chromosomal segments. Here, a subARG is constructed independently for each of five gene-free regions across the X chromosome, and the results are aggregated across them. For PCA, MDS and ancestry inference with STRUCTURE, the subARG is processed to obtain feature vectors of samples and pairwise distances between samples. The observed population structure, estimated from the five short X chromosomal segments, supports genome-wide frequency-based analyses: African populations show higher genetic diversity, and the general trend of shared variation is seen across the globe from Africa through Middle East, Europe, Central Asia, Southeast Asia, and East Asia in broad patterns. The recombinational analysis was also compared with established methods based on SNPs and haplotypes. For haplotypes, we also employed a fixed-length approach based on information-content optimization. Our recombinational analysis suggested a southern migration route out of Africa, and it also supports a single, rapid human expansion from Africa to East Asia through South Asia.
eu_rights_str_mv openAccess
format article
id LAURepo_dc3e0a7dde9c9a084d227e565471fc74
identifier_str_mv 1432-1203
Javed, A., Melé, M., Pybus, M., Zalloua, P., Haber, M., Comas, D., ... & Yang, Y. (2012). Recombination networks as genetic markers in a human variation study of the Old World. Human genetics, 131(4), 601-613.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/11118
publishDate 2012
repository.mail.fl_str_mv
repository.name.fl_str_mv
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spelling Recombination networks as genetic markers in a human variation study of the Old WorldJaved, AsifMele, MartaPybus, MarcZalloua, PierreHaber, MarcComas, DavidNetea, Mihai G.Balanovsky, OlegBalanovsky, ElenaJin, LiYang, YajunArunKumar, GaneshPrasadPitchappan, RamasamyBertranpetit, JaumeCalafell, FrancescWe have analyzed human genetic diversity in 33 Old World populations including 23 populations obtained through Genographic Project studies. A set of 1,536 SNPs in five X chromosome regions were genotyped in 1,288 individuals (mostly males). We use a novel analysis employing subARG network construction with recombining chromosomal segments. Here, a subARG is constructed independently for each of five gene-free regions across the X chromosome, and the results are aggregated across them. For PCA, MDS and ancestry inference with STRUCTURE, the subARG is processed to obtain feature vectors of samples and pairwise distances between samples. The observed population structure, estimated from the five short X chromosomal segments, supports genome-wide frequency-based analyses: African populations show higher genetic diversity, and the general trend of shared variation is seen across the globe from Africa through Middle East, Europe, Central Asia, Southeast Asia, and East Asia in broad patterns. The recombinational analysis was also compared with established methods based on SNPs and haplotypes. For haplotypes, we also employed a fixed-length approach based on information-content optimization. Our recombinational analysis suggested a southern migration route out of Africa, and it also supports a single, rapid human expansion from Africa to East Asia through South Asia.PublishedN/A2019-07-22T08:02:46Z2019-07-22T08:02:46Z20122019-07-22Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1432-1203http://hdl.handle.net/10725/11118https://doi.org/10.1007/s00439-011-1104-8Javed, A., Melé, M., Pybus, M., Zalloua, P., Haber, M., Comas, D., ... & Yang, Y. (2012). Recombination networks as genetic markers in a human variation study of the Old World. Human genetics, 131(4), 601-613.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttps://link.springer.com/article/10.1007/s00439-011-1104-8enHuman Geneticsinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/111182021-03-19T10:47:35Z
spellingShingle Recombination networks as genetic markers in a human variation study of the Old World
Javed, Asif
status_str publishedVersion
title Recombination networks as genetic markers in a human variation study of the Old World
title_full Recombination networks as genetic markers in a human variation study of the Old World
title_fullStr Recombination networks as genetic markers in a human variation study of the Old World
title_full_unstemmed Recombination networks as genetic markers in a human variation study of the Old World
title_short Recombination networks as genetic markers in a human variation study of the Old World
title_sort Recombination networks as genetic markers in a human variation study of the Old World
url http://hdl.handle.net/10725/11118
https://doi.org/10.1007/s00439-011-1104-8
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
https://link.springer.com/article/10.1007/s00439-011-1104-8