Population genetic analyses of the NGM STR loci
The AmpFlSTR® NGM™ PCR Amplification Kit enables amplification of 15 autosomal short tandem repeat (STR) loci. The loci are the ten STRs in the SGM Plus® Kit plus the EDNAP and ENSFI recommended STRs D10S1248, D22S1045, D2S441, D1S1656, and D12S391. Allele frequency and other forensically relevant s...
Gespeichert in:
Veröffentlicht in: | International journal of legal medicine 2011-01, Vol.125 (1), p.101-109 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 109 |
---|---|
container_issue | 1 |
container_start_page | 101 |
container_title | International journal of legal medicine |
container_volume | 125 |
creator | Budowle, Bruce Ge, Jianye Chakraborty, Ranajit Eisenberg, Arthur J. Green, Robert Mulero, Julio Lagace, Robert Hennessy, Lori |
description | The AmpFlSTR® NGM™ PCR Amplification Kit enables amplification of 15 autosomal short tandem repeat (STR) loci. The loci are the ten STRs in the SGM Plus® Kit plus the EDNAP and ENSFI recommended STRs D10S1248, D22S1045, D2S441, D1S1656, and D12S391. Allele frequency and other forensically relevant statistics data were generated for the NGM loci in three US population groups (African Americans, Caucasians, and Hispanics). The analyses support that the NGM multiplex is one of the most informative STR multiplex kits available to the forensic science community. At the population level, there are no more detectable departures from expectations of the independence of alleles within as well as between loci than would be expected due to chance, even for the two syntenic loci vWA and D12S391; however, linkage analysis in three large pedigree families shows close linkage between these two loci with a recombination fraction of 0.108. Therefore, in contrast to the practices in calculating the rarity of a DNA profile, for kinship analyses independence between the loci, vWA and D12S391 cannot be assumed. |
doi_str_mv | 10.1007/s00414-010-0516-7 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_954617372</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>822555690</sourcerecordid><originalsourceid>FETCH-LOGICAL-c435t-30934b8b93c770fd6a830443331763c6bfa4ecf8f2a9c77ca1c2be8e092cdaaa3</originalsourceid><addsrcrecordid>eNqFkE1LAzEQhoMotlZ_gBdZvHhaO_naJEcpWoX6gdZzyKbZumW7qZvdQ_-9qa0KgniawDzzzuRB6BTDJQYQwwDAMEsBQwocZ6nYQ33MqEgxV9k-6oOKbyWJ6KGjEBYAWGSCH6IeASkkw7yPhk9-1VWmLX2dzF3t2tImpjbVOriQ-CJp31zyML5PXqbPSeVteYwOClMFd7KrA_R6cz0d3aaTx_Hd6GqSWkZ5m9K4muUyV9QKAcUsM5ICY5TSeAK1WV4Y5mwhC2JUJKzBluROOlDEzowxdIAutrmrxr93LrR6WQbrqsrUzndBK84yLKgg_5KSEM55piCS57_Ihe-a-NlPCLjggCOEt5BtfAiNK_SqKZemWWsMemNdb63raF1vrGsRZ852wV2-dLPviS_NESBbIMRWPXfNz-a_Uz8A2AWJ7g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>822057501</pqid></control><display><type>article</type><title>Population genetic analyses of the NGM STR loci</title><source>MEDLINE</source><source>HeinOnline Law Journal Library</source><source>SpringerNature Journals</source><creator>Budowle, Bruce ; Ge, Jianye ; Chakraborty, Ranajit ; Eisenberg, Arthur J. ; Green, Robert ; Mulero, Julio ; Lagace, Robert ; Hennessy, Lori</creator><creatorcontrib>Budowle, Bruce ; Ge, Jianye ; Chakraborty, Ranajit ; Eisenberg, Arthur J. ; Green, Robert ; Mulero, Julio ; Lagace, Robert ; Hennessy, Lori</creatorcontrib><description>The AmpFlSTR® NGM™ PCR Amplification Kit enables amplification of 15 autosomal short tandem repeat (STR) loci. The loci are the ten STRs in the SGM Plus® Kit plus the EDNAP and ENSFI recommended STRs D10S1248, D22S1045, D2S441, D1S1656, and D12S391. Allele frequency and other forensically relevant statistics data were generated for the NGM loci in three US population groups (African Americans, Caucasians, and Hispanics). The analyses support that the NGM multiplex is one of the most informative STR multiplex kits available to the forensic science community. At the population level, there are no more detectable departures from expectations of the independence of alleles within as well as between loci than would be expected due to chance, even for the two syntenic loci vWA and D12S391; however, linkage analysis in three large pedigree families shows close linkage between these two loci with a recombination fraction of 0.108. Therefore, in contrast to the practices in calculating the rarity of a DNA profile, for kinship analyses independence between the loci, vWA and D12S391 cannot be assumed.</description><identifier>ISSN: 0937-9827</identifier><identifier>EISSN: 1437-1596</identifier><identifier>DOI: 10.1007/s00414-010-0516-7</identifier><identifier>PMID: 20878415</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Continental Population Groups - genetics ; DNA Fingerprinting - methods ; Forensic Medicine ; Forensic sciences ; Gene Frequency ; Genetic Linkage ; Genetics, Population ; Humans ; Medical Law ; Medicine ; Medicine & Public Health ; Polymerase Chain Reaction ; Tandem Repeat Sequences ; Technical Note ; United States</subject><ispartof>International journal of legal medicine, 2011-01, Vol.125 (1), p.101-109</ispartof><rights>Springer-Verlag 2010</rights><rights>Springer-Verlag 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-30934b8b93c770fd6a830443331763c6bfa4ecf8f2a9c77ca1c2be8e092cdaaa3</citedby><cites>FETCH-LOGICAL-c435t-30934b8b93c770fd6a830443331763c6bfa4ecf8f2a9c77ca1c2be8e092cdaaa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00414-010-0516-7$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00414-010-0516-7$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20878415$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Budowle, Bruce</creatorcontrib><creatorcontrib>Ge, Jianye</creatorcontrib><creatorcontrib>Chakraborty, Ranajit</creatorcontrib><creatorcontrib>Eisenberg, Arthur J.</creatorcontrib><creatorcontrib>Green, Robert</creatorcontrib><creatorcontrib>Mulero, Julio</creatorcontrib><creatorcontrib>Lagace, Robert</creatorcontrib><creatorcontrib>Hennessy, Lori</creatorcontrib><title>Population genetic analyses of the NGM STR loci</title><title>International journal of legal medicine</title><addtitle>Int J Legal Med</addtitle><addtitle>Int J Legal Med</addtitle><description>The AmpFlSTR® NGM™ PCR Amplification Kit enables amplification of 15 autosomal short tandem repeat (STR) loci. The loci are the ten STRs in the SGM Plus® Kit plus the EDNAP and ENSFI recommended STRs D10S1248, D22S1045, D2S441, D1S1656, and D12S391. Allele frequency and other forensically relevant statistics data were generated for the NGM loci in three US population groups (African Americans, Caucasians, and Hispanics). The analyses support that the NGM multiplex is one of the most informative STR multiplex kits available to the forensic science community. At the population level, there are no more detectable departures from expectations of the independence of alleles within as well as between loci than would be expected due to chance, even for the two syntenic loci vWA and D12S391; however, linkage analysis in three large pedigree families shows close linkage between these two loci with a recombination fraction of 0.108. Therefore, in contrast to the practices in calculating the rarity of a DNA profile, for kinship analyses independence between the loci, vWA and D12S391 cannot be assumed.</description><subject>Continental Population Groups - genetics</subject><subject>DNA Fingerprinting - methods</subject><subject>Forensic Medicine</subject><subject>Forensic sciences</subject><subject>Gene Frequency</subject><subject>Genetic Linkage</subject><subject>Genetics, Population</subject><subject>Humans</subject><subject>Medical Law</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Polymerase Chain Reaction</subject><subject>Tandem Repeat Sequences</subject><subject>Technical Note</subject><subject>United States</subject><issn>0937-9827</issn><issn>1437-1596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqFkE1LAzEQhoMotlZ_gBdZvHhaO_naJEcpWoX6gdZzyKbZumW7qZvdQ_-9qa0KgniawDzzzuRB6BTDJQYQwwDAMEsBQwocZ6nYQ33MqEgxV9k-6oOKbyWJ6KGjEBYAWGSCH6IeASkkw7yPhk9-1VWmLX2dzF3t2tImpjbVOriQ-CJp31zyML5PXqbPSeVteYwOClMFd7KrA_R6cz0d3aaTx_Hd6GqSWkZ5m9K4muUyV9QKAcUsM5ICY5TSeAK1WV4Y5mwhC2JUJKzBluROOlDEzowxdIAutrmrxr93LrR6WQbrqsrUzndBK84yLKgg_5KSEM55piCS57_Ihe-a-NlPCLjggCOEt5BtfAiNK_SqKZemWWsMemNdb63raF1vrGsRZ852wV2-dLPviS_NESBbIMRWPXfNz-a_Uz8A2AWJ7g</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Budowle, Bruce</creator><creator>Ge, Jianye</creator><creator>Chakraborty, Ranajit</creator><creator>Eisenberg, Arthur J.</creator><creator>Green, Robert</creator><creator>Mulero, Julio</creator><creator>Lagace, Robert</creator><creator>Hennessy, Lori</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>0-V</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AM</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BGRYB</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>HCIFZ</scope><scope>K7.</scope><scope>K9.</scope><scope>L6V</scope><scope>M0O</scope><scope>M0S</scope><scope>M1P</scope><scope>M7S</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7X8</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20110101</creationdate><title>Population genetic analyses of the NGM STR loci</title><author>Budowle, Bruce ; Ge, Jianye ; Chakraborty, Ranajit ; Eisenberg, Arthur J. ; Green, Robert ; Mulero, Julio ; Lagace, Robert ; Hennessy, Lori</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-30934b8b93c770fd6a830443331763c6bfa4ecf8f2a9c77ca1c2be8e092cdaaa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Continental Population Groups - genetics</topic><topic>DNA Fingerprinting - methods</topic><topic>Forensic Medicine</topic><topic>Forensic sciences</topic><topic>Gene Frequency</topic><topic>Genetic Linkage</topic><topic>Genetics, Population</topic><topic>Humans</topic><topic>Medical Law</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Polymerase Chain Reaction</topic><topic>Tandem Repeat Sequences</topic><topic>Technical Note</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Budowle, Bruce</creatorcontrib><creatorcontrib>Ge, Jianye</creatorcontrib><creatorcontrib>Chakraborty, Ranajit</creatorcontrib><creatorcontrib>Eisenberg, Arthur J.</creatorcontrib><creatorcontrib>Green, Robert</creatorcontrib><creatorcontrib>Mulero, Julio</creatorcontrib><creatorcontrib>Lagace, Robert</creatorcontrib><creatorcontrib>Hennessy, Lori</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Criminal Justice Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Criminology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Criminal Justice (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>Criminal Justice Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Engineering Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>International journal of legal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Budowle, Bruce</au><au>Ge, Jianye</au><au>Chakraborty, Ranajit</au><au>Eisenberg, Arthur J.</au><au>Green, Robert</au><au>Mulero, Julio</au><au>Lagace, Robert</au><au>Hennessy, Lori</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Population genetic analyses of the NGM STR loci</atitle><jtitle>International journal of legal medicine</jtitle><stitle>Int J Legal Med</stitle><addtitle>Int J Legal Med</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>125</volume><issue>1</issue><spage>101</spage><epage>109</epage><pages>101-109</pages><issn>0937-9827</issn><eissn>1437-1596</eissn><abstract>The AmpFlSTR® NGM™ PCR Amplification Kit enables amplification of 15 autosomal short tandem repeat (STR) loci. The loci are the ten STRs in the SGM Plus® Kit plus the EDNAP and ENSFI recommended STRs D10S1248, D22S1045, D2S441, D1S1656, and D12S391. Allele frequency and other forensically relevant statistics data were generated for the NGM loci in three US population groups (African Americans, Caucasians, and Hispanics). The analyses support that the NGM multiplex is one of the most informative STR multiplex kits available to the forensic science community. At the population level, there are no more detectable departures from expectations of the independence of alleles within as well as between loci than would be expected due to chance, even for the two syntenic loci vWA and D12S391; however, linkage analysis in three large pedigree families shows close linkage between these two loci with a recombination fraction of 0.108. Therefore, in contrast to the practices in calculating the rarity of a DNA profile, for kinship analyses independence between the loci, vWA and D12S391 cannot be assumed.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>20878415</pmid><doi>10.1007/s00414-010-0516-7</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0937-9827 |
ispartof | International journal of legal medicine, 2011-01, Vol.125 (1), p.101-109 |
issn | 0937-9827 1437-1596 |
language | eng |
recordid | cdi_proquest_miscellaneous_954617372 |
source | MEDLINE; HeinOnline Law Journal Library; SpringerNature Journals |
subjects | Continental Population Groups - genetics DNA Fingerprinting - methods Forensic Medicine Forensic sciences Gene Frequency Genetic Linkage Genetics, Population Humans Medical Law Medicine Medicine & Public Health Polymerase Chain Reaction Tandem Repeat Sequences Technical Note United States |
title | Population genetic analyses of the NGM STR loci |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T08%3A58%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Population%20genetic%20analyses%20of%20the%20NGM%20STR%20loci&rft.jtitle=International%20journal%20of%20legal%20medicine&rft.au=Budowle,%20Bruce&rft.date=2011-01-01&rft.volume=125&rft.issue=1&rft.spage=101&rft.epage=109&rft.pages=101-109&rft.issn=0937-9827&rft.eissn=1437-1596&rft_id=info:doi/10.1007/s00414-010-0516-7&rft_dat=%3Cproquest_cross%3E822555690%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=822057501&rft_id=info:pmid/20878415&rfr_iscdi=true |