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SNPSTR rs59186128_D7S820 polymorphism distribution in European Caucasoid, Hispanic, and Afro-American populations
Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the course of evolution, so analysing them can help dist...
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Published in: | International journal of legal medicine 2009-11, Vol.123 (6), p.527-533 |
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container_title | International journal of legal medicine |
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creator | Odriozola, A. Aznar, J. M. Valverde, L. Cardoso, S. Bravo, M. L. Builes, J. J. Martínez, B. Sanchez, D. González-Andrade, F. Sarasola, E. González-Fernández, M. C. Jarreta, B. Martínez De Pancorbo, Marian M. |
description | Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the course of evolution, so analysing them can help distinguish between STR alleles in which the number of repetitions matches due to descent from those which match by chance. This provides support for the determination of biological paternity and other kinship analyses in which mutation needs to be ruled out as grounds for exclusion. Locus D7S820 shows a variable position, SNP
rs59186128,
in the 5′ flanking region. This study is set out (1) to determine the frequencies of SNP
rs59186128
in populations with various geographical origins and (2) to estimate the possible contribution of
rs59186128
to the allele discrimination of locus D7S820. To that end, individuals from European Caucasoid, Hispanic, and Afro-American populations are studied using denaturing high-performance liquid chromatography, which enables locus
rs59186128
to be quickly and highly cost-effectively screened. Moreover, a method is established for determining the haplotypes of SNPSTR
rs59186128_
D7820. The results show that SNP
rs59186128
has a T allele frequency of more than 0.15 in one of the Afro-American populations studied, and the haplotype analysis shows that there is no preferential association between the alleles of SNPSTR
rs59186128
_D7S820, which supports the idea that they could be useful in forensic applications. |
doi_str_mv | 10.1007/s00414-009-0370-7 |
format | article |
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rs59186128,
in the 5′ flanking region. This study is set out (1) to determine the frequencies of SNP
rs59186128
in populations with various geographical origins and (2) to estimate the possible contribution of
rs59186128
to the allele discrimination of locus D7S820. To that end, individuals from European Caucasoid, Hispanic, and Afro-American populations are studied using denaturing high-performance liquid chromatography, which enables locus
rs59186128
to be quickly and highly cost-effectively screened. Moreover, a method is established for determining the haplotypes of SNPSTR
rs59186128_
D7820. The results show that SNP
rs59186128
has a T allele frequency of more than 0.15 in one of the Afro-American populations studied, and the haplotype analysis shows that there is no preferential association between the alleles of SNPSTR
rs59186128
_D7S820, which supports the idea that they could be useful in forensic applications.</description><identifier>ISSN: 0937-9827</identifier><identifier>EISSN: 1437-1596</identifier><identifier>DOI: 10.1007/s00414-009-0370-7</identifier><identifier>PMID: 19693525</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Chromatography ; Chromatography, High Pressure Liquid ; Continental Population Groups - genetics ; DNA Fingerprinting ; Forensic Medicine ; Gene Frequency ; Genetic testing ; Genetics, Population ; Genomes ; Genotype ; Haplotypes ; Hispanic people ; Humans ; Medical Law ; Medicine ; Medicine & Public Health ; Mutation ; Polymorphism ; Polymorphism, Single Nucleotide ; Short Communication ; Tandem Repeat Sequences</subject><ispartof>International journal of legal medicine, 2009-11, Vol.123 (6), p.527-533</ispartof><rights>Springer-Verlag 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c370t-6c3bd86c30fcabefef77181dd4d3f439f944d38a924f1f3741330fd2a0d898193</citedby><cites>FETCH-LOGICAL-c370t-6c3bd86c30fcabefef77181dd4d3f439f944d38a924f1f3741330fd2a0d898193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/216617687/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/216617687?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,776,780,21356,21374,27903,27904,33590,33591,33748,33749,43712,43793,73967,74056</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19693525$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Odriozola, A.</creatorcontrib><creatorcontrib>Aznar, J. M.</creatorcontrib><creatorcontrib>Valverde, L.</creatorcontrib><creatorcontrib>Cardoso, S.</creatorcontrib><creatorcontrib>Bravo, M. L.</creatorcontrib><creatorcontrib>Builes, J. J.</creatorcontrib><creatorcontrib>Martínez, B.</creatorcontrib><creatorcontrib>Sanchez, D.</creatorcontrib><creatorcontrib>González-Andrade, F.</creatorcontrib><creatorcontrib>Sarasola, E.</creatorcontrib><creatorcontrib>González-Fernández, M. C.</creatorcontrib><creatorcontrib>Jarreta, B. Martínez</creatorcontrib><creatorcontrib>De Pancorbo, Marian M.</creatorcontrib><title>SNPSTR rs59186128_D7S820 polymorphism distribution in European Caucasoid, Hispanic, and Afro-American populations</title><title>International journal of legal medicine</title><addtitle>Int J Legal Med</addtitle><addtitle>Int J Legal Med</addtitle><description>Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the course of evolution, so analysing them can help distinguish between STR alleles in which the number of repetitions matches due to descent from those which match by chance. This provides support for the determination of biological paternity and other kinship analyses in which mutation needs to be ruled out as grounds for exclusion. Locus D7S820 shows a variable position, SNP
rs59186128,
in the 5′ flanking region. This study is set out (1) to determine the frequencies of SNP
rs59186128
in populations with various geographical origins and (2) to estimate the possible contribution of
rs59186128
to the allele discrimination of locus D7S820. To that end, individuals from European Caucasoid, Hispanic, and Afro-American populations are studied using denaturing high-performance liquid chromatography, which enables locus
rs59186128
to be quickly and highly cost-effectively screened. Moreover, a method is established for determining the haplotypes of SNPSTR
rs59186128_
D7820. The results show that SNP
rs59186128
has a T allele frequency of more than 0.15 in one of the Afro-American populations studied, and the haplotype analysis shows that there is no preferential association between the alleles of SNPSTR
rs59186128
_D7S820, which supports the idea that they could be useful in forensic applications.</description><subject>Chromatography</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Continental Population Groups - genetics</subject><subject>DNA Fingerprinting</subject><subject>Forensic Medicine</subject><subject>Gene Frequency</subject><subject>Genetic testing</subject><subject>Genetics, Population</subject><subject>Genomes</subject><subject>Genotype</subject><subject>Haplotypes</subject><subject>Hispanic people</subject><subject>Humans</subject><subject>Medical Law</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mutation</subject><subject>Polymorphism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Short Communication</subject><subject>Tandem Repeat Sequences</subject><issn>0937-9827</issn><issn>1437-1596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>ALSLI</sourceid><sourceid>BGRYB</sourceid><sourceid>M0O</sourceid><recordid>eNp1kUFP3DAQha2Kqmxpf0AvyOLChZSZ2Int42qhUAm1qEvPlje2i1ESB3tz4N_j1a6EhNSLPdJ879kzj5BvCN8RQFxmAI68AlAVMAGV-EAWyJmosFHtEVmAKrWStTgmn3N-AkDRiuYTOUbVKtbUzYI8r3_drx_-0JQbhbLFWuorsZY10Cn2L0NM02PIA7Uhb1PYzNsQRxpGej2nODkz0pWZO5NjsBf0NuTJjKG7oGa0dOlTrJaDS6Er2BSnuTc7df5CPnrTZ_f1cJ-Qvz-uH1a31d3vm5-r5V3VlVG2VduxjZXlBN-ZjfPOC4ESreWWec6UV7xU0qiae_RMcGQFtbUBK5VExU7I-d53SvF5dnmrh5A71_dmdHHOWjAOSnLVFvLsHfkU5zSWz-ka27YsTYoC4R7qUsw5Oa-nFAaTXjSC3qWh92nokobepaF3mtOD8bwZnH1THNZfgHoP5NIa_7n09vL_XV8BHHeTag</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Odriozola, A.</creator><creator>Aznar, J. 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M. ; Valverde, L. ; Cardoso, S. ; Bravo, M. L. ; Builes, J. J. ; Martínez, B. ; Sanchez, D. ; González-Andrade, F. ; Sarasola, E. ; González-Fernández, M. C. ; Jarreta, B. 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M.</creatorcontrib><creatorcontrib>Valverde, L.</creatorcontrib><creatorcontrib>Cardoso, S.</creatorcontrib><creatorcontrib>Bravo, M. L.</creatorcontrib><creatorcontrib>Builes, J. J.</creatorcontrib><creatorcontrib>Martínez, B.</creatorcontrib><creatorcontrib>Sanchez, D.</creatorcontrib><creatorcontrib>González-Andrade, F.</creatorcontrib><creatorcontrib>Sarasola, E.</creatorcontrib><creatorcontrib>González-Fernández, M. C.</creatorcontrib><creatorcontrib>Jarreta, B. Martínez</creatorcontrib><creatorcontrib>De Pancorbo, Marian M.</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【Remote access available】</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)</collection><collection>ProQuest Central</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><jtitle>International journal of legal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Odriozola, A.</au><au>Aznar, J. M.</au><au>Valverde, L.</au><au>Cardoso, S.</au><au>Bravo, M. L.</au><au>Builes, J. J.</au><au>Martínez, B.</au><au>Sanchez, D.</au><au>González-Andrade, F.</au><au>Sarasola, E.</au><au>González-Fernández, M. C.</au><au>Jarreta, B. Martínez</au><au>De Pancorbo, Marian M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>SNPSTR rs59186128_D7S820 polymorphism distribution in European Caucasoid, Hispanic, and Afro-American populations</atitle><jtitle>International journal of legal medicine</jtitle><stitle>Int J Legal Med</stitle><addtitle>Int J Legal Med</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>123</volume><issue>6</issue><spage>527</spage><epage>533</epage><pages>527-533</pages><issn>0937-9827</issn><eissn>1437-1596</eissn><abstract>Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the course of evolution, so analysing them can help distinguish between STR alleles in which the number of repetitions matches due to descent from those which match by chance. This provides support for the determination of biological paternity and other kinship analyses in which mutation needs to be ruled out as grounds for exclusion. Locus D7S820 shows a variable position, SNP
rs59186128,
in the 5′ flanking region. This study is set out (1) to determine the frequencies of SNP
rs59186128
in populations with various geographical origins and (2) to estimate the possible contribution of
rs59186128
to the allele discrimination of locus D7S820. To that end, individuals from European Caucasoid, Hispanic, and Afro-American populations are studied using denaturing high-performance liquid chromatography, which enables locus
rs59186128
to be quickly and highly cost-effectively screened. Moreover, a method is established for determining the haplotypes of SNPSTR
rs59186128_
D7820. The results show that SNP
rs59186128
has a T allele frequency of more than 0.15 in one of the Afro-American populations studied, and the haplotype analysis shows that there is no preferential association between the alleles of SNPSTR
rs59186128
_D7S820, which supports the idea that they could be useful in forensic applications.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>19693525</pmid><doi>10.1007/s00414-009-0370-7</doi><tpages>7</tpages></addata></record> |
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source | Criminology Collection; Social Science Premium Collection; Springer Link |
subjects | Chromatography Chromatography, High Pressure Liquid Continental Population Groups - genetics DNA Fingerprinting Forensic Medicine Gene Frequency Genetic testing Genetics, Population Genomes Genotype Haplotypes Hispanic people Humans Medical Law Medicine Medicine & Public Health Mutation Polymorphism Polymorphism, Single Nucleotide Short Communication Tandem Repeat Sequences |
title | SNPSTR rs59186128_D7S820 polymorphism distribution in European Caucasoid, Hispanic, and Afro-American populations |
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