Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.

The authors have used an online community approach, and tools that were readily available via the Internet, to discover genealogically and therefore phylogenetically relevant Y-chromosome polymorphisms within core haplogroup R1b1a2-L11/S127 (rs9786076). Presented here is the analysis of 135 unrelate...

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Main Authors: Richard A Rocca, Gregory Magoon, David F Reynolds, Thomas Krahn, Vincent O Tilroe, Peter M Op den Velde Boots, Andrew J Grierson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3404022?pdf=render
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spelling doaj-593a02d53d0d4e07840e30dc49057d9d2020-11-25T01:48:10ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4163410.1371/journal.pone.0041634Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.Richard A RoccaGregory MagoonDavid F ReynoldsThomas KrahnVincent O TilroePeter M Op den Velde BootsAndrew J GriersonThe authors have used an online community approach, and tools that were readily available via the Internet, to discover genealogically and therefore phylogenetically relevant Y-chromosome polymorphisms within core haplogroup R1b1a2-L11/S127 (rs9786076). Presented here is the analysis of 135 unrelated L11 derived samples from the 1000 Genomes Project. We were able to discover new variants and build a much more complex phylogenetic relationship for L11 sub-clades. Many of the variants were further validated using PCR amplification and Sanger sequencing. The identification of these new variants will help further the understanding of population history including patrilineal migrations in Western and Central Europe where R1b1a2 is the most frequent haplogroup. The fine-grained phylogenetic tree we present here will also help to refine historical genetic dating studies. Our findings demonstrate the power of citizen science for analysis of whole genome sequence data.http://europepmc.org/articles/PMC3404022?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Richard A Rocca
Gregory Magoon
David F Reynolds
Thomas Krahn
Vincent O Tilroe
Peter M Op den Velde Boots
Andrew J Grierson
spellingShingle Richard A Rocca
Gregory Magoon
David F Reynolds
Thomas Krahn
Vincent O Tilroe
Peter M Op den Velde Boots
Andrew J Grierson
Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.
PLoS ONE
author_facet Richard A Rocca
Gregory Magoon
David F Reynolds
Thomas Krahn
Vincent O Tilroe
Peter M Op den Velde Boots
Andrew J Grierson
author_sort Richard A Rocca
title Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.
title_short Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.
title_full Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.
title_fullStr Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.
title_full_unstemmed Discovery of Western European R1b1a2 Y chromosome variants in 1000 genomes project data: an online community approach.
title_sort discovery of western european r1b1a2 y chromosome variants in 1000 genomes project data: an online community approach.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description The authors have used an online community approach, and tools that were readily available via the Internet, to discover genealogically and therefore phylogenetically relevant Y-chromosome polymorphisms within core haplogroup R1b1a2-L11/S127 (rs9786076). Presented here is the analysis of 135 unrelated L11 derived samples from the 1000 Genomes Project. We were able to discover new variants and build a much more complex phylogenetic relationship for L11 sub-clades. Many of the variants were further validated using PCR amplification and Sanger sequencing. The identification of these new variants will help further the understanding of population history including patrilineal migrations in Western and Central Europe where R1b1a2 is the most frequent haplogroup. The fine-grained phylogenetic tree we present here will also help to refine historical genetic dating studies. Our findings demonstrate the power of citizen science for analysis of whole genome sequence data.
url http://europepmc.org/articles/PMC3404022?pdf=render
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