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dc.contributor.authorSinha, Priyanka
dc.contributor.authorDincer, Aslihan
dc.contributor.authorVirgil, Daniel
dc.contributor.authorXu, Guang
dc.contributor.authorPoh, Yu-Ping
dc.contributor.authorJensen, Jeffrey D.
dc.date2022-08-11T08:08:54.000
dc.date.accessioned2022-08-23T16:11:44Z
dc.date.available2022-08-23T16:11:44Z
dc.date.issued2011-12-01
dc.date.submitted2012-04-11
dc.identifier.citationSinha P, Dincer A, Virgil D, Xu G, Poh Y-P and Jensen JD (2011) On detecting selective sweeps using single genomes. Front. Gene. 2:85. doi: 10.3389/fgene.2011.00085. <a href="http://dx.doi.org/10.3389/fgene.2011.00085">Link to article on publisher's website</a>
dc.identifier.issn1664-8021
dc.identifier.doi10.3389/fgene.2011.00085
dc.identifier.pmid22303379
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33241
dc.description.abstractIdentifying the genetic basis of human adaptation has remained a central focal point of modern population genetics. One major area of interest has been the use of polymorphism data to detect so-called "footprints" of selective sweeps - patterns produced as a beneficial mutation arises and rapidly fixes in the population. Based on numerous simulation studies and power analyses, the necessary sample size for achieving appreciable power has been shown to vary from a few individuals to a few dozen, depending on the test statistic. And yet, the sequencing of multiple copies of a single region, or of multiple genomes as is now often the case, incurs considerable cost. Enard et al. (2010) have recently proposed a method to identify patterns of selective sweeps using a single genome - and apply this approach to human and non-human primates (chimpanzee, orangutan, and macaque). They employ essentially a modification of the Hudson, Kreitman, and Aguade test - using heterozygous single nucleotide polymorphisms from single individuals, and divergence data from two closely related species (human-chimpanzee, human-orangutan, and human-macaque). Given the potential importance of this finding, we here investigate the properties of this statistic. We demonstrate through simulation that this approach is neither robust to demography nor background selection; nor is it robust to variable recombination rates.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=22303379&dopt=Abstract">Link to article in PubMed</a>
dc.rights<p>Copyright: © 2011 Sinha, Dincer, Virgil, Xu, Poh and Jensen. This is an open-access article distributed under the terms of the <a href="http://creativecommons.org/licenses/by-nc/3.0/">Creative Commons Attribution Non Commercial License</a>, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.</p>
dc.subjectAdaptation, Biological; Polymorphism, Genetic; Genetics, Population; Genomics
dc.subjectBioinformatics
dc.subjectGenetics and Genomics
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleOn detecting selective sweeps using single genomes
dc.typeJournal Article
dc.source.journaltitleFrontiers in Genetics
dc.source.volume2
dc.source.issue85
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=2786&amp;context=gsbs_sp&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1776
dc.identifier.contextkey2756270
refterms.dateFOA2022-08-23T16:11:45Z
html.description.abstract<p>Identifying the genetic basis of human adaptation has remained a central focal point of modern population genetics. One major area of interest has been the use of polymorphism data to detect so-called "footprints" of selective sweeps - patterns produced as a beneficial mutation arises and rapidly fixes in the population. Based on numerous simulation studies and power analyses, the necessary sample size for achieving appreciable power has been shown to vary from a few individuals to a few dozen, depending on the test statistic. And yet, the sequencing of multiple copies of a single region, or of multiple genomes as is now often the case, incurs considerable cost. Enard et al. (2010) have recently proposed a method to identify patterns of selective sweeps using a single genome - and apply this approach to human and non-human primates (chimpanzee, orangutan, and macaque). They employ essentially a modification of the Hudson, Kreitman, and Aguade test - using heterozygous single nucleotide polymorphisms from single individuals, and divergence data from two closely related species (human-chimpanzee, human-orangutan, and human-macaque). Given the potential importance of this finding, we here investigate the properties of this statistic. We demonstrate through simulation that this approach is neither robust to demography nor background selection; nor is it robust to variable recombination rates.</p>
dc.identifier.submissionpathgsbs_sp/1776
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.contributor.studentAslihan Dincer; Daniel Virgil; Guang Xu


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