Genetic variation of 10 X chromosomal STR loci in Indian population
X chromosomal short tandem repeats have the potential to complement the analyses of the autosomal, Y chromosomal, and mitochondrial DNA markers in forensics and population genetics, and extensive research on X chromosomal markers is being carried out. In the present study, a decaplex for the co-ampl...
Gespeichert in:
Veröffentlicht in: | International journal of legal medicine 2010-07, Vol.124 (4), p.327-330 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 330 |
---|---|
container_issue | 4 |
container_start_page | 327 |
container_title | International journal of legal medicine |
container_volume | 124 |
creator | Mukerjee, Sanjukta Ghosh, Tania Kalpana, D. Mukherjee, Meeta Sharma, Anil Kumar |
description | X chromosomal short tandem repeats have the potential to complement the analyses of the autosomal, Y chromosomal, and mitochondrial DNA markers in forensics and population genetics, and extensive research on X chromosomal markers is being carried out. In the present study, a decaplex for the co-amplification of ten X chromosomal microsatellite loci (DXS6807, DXS8378, DXS7132, DXS6809, DXS6789, DXS101, DXS7133, GATA172D05, HPRTB, and GATA31E08) was optimized and 749 blood samples of unrelated male individuals from the four major linguistic families of India were analyzed. The number of alleles for the studied loci ranged from 7–16 while the gene diversity values varied from 0.408 to 0.855. Two new alleles were observed for the loci DXS101 and HPRTB. Statistical parameters of forensic interest were calculated and all loci were found to be polymorphic. High power of discrimination was observed for the loci DXS101, DXS6809, and DXS6789. The present study demonstrates the efficacy of these X-linked markers for human identification and kinship analysis. |
doi_str_mv | 10.1007/s00414-010-0456-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_745940010</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>733305987</sourcerecordid><originalsourceid>FETCH-LOGICAL-c402t-e4cd3de8d4fab2e1d01c166ba04f0fe78a30febb4e7f90e83147ef585eb78f343</originalsourceid><addsrcrecordid>eNqFkVtLxDAQhYMoul5-gC8SfPGpOrk17aMsugqC4AV8C2k70UrbrMlW8N-bdb2AID7NwHznDDOHkH0GxwxAn0QAyWQGDDKQKs_4GpkwKXTGVJmvkwmUqS8LrrfIdozPAEznWm2SLQ6Scw5qQqYzHHDR1vTVhtYuWj9Q7ygD-kDrp-B7H31vO3p7d0M7X7e0Hejl0LR2oHM_H7sPxS7ZcLaLuPdZd8j9-dnd9CK7up5dTk-vsloCX2Qo60Y0WDTS2Yoja4DVLM8rC9KBQ11YkUpVSdSuBCwEkxqdKhRWunBCih1ytPKdB_8yYlyYvo01dp0d0I_RaKlKmY6E_0khBKiy0Ik8_EU--zEM6QyjQAJjmi_t2Aqqg48xoDPz0PY2vBkGZpmEWSVh0m6zTMLwpDn4NB6rHptvxdfrE8BXQEyj4RHDz-a_Xd8BYw-RiQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>504011720</pqid></control><display><type>article</type><title>Genetic variation of 10 X chromosomal STR loci in Indian population</title><source>MEDLINE</source><source>HeinOnline Law Journal Library</source><source>SpringerLink Journals - AutoHoldings</source><creator>Mukerjee, Sanjukta ; Ghosh, Tania ; Kalpana, D. ; Mukherjee, Meeta ; Sharma, Anil Kumar</creator><creatorcontrib>Mukerjee, Sanjukta ; Ghosh, Tania ; Kalpana, D. ; Mukherjee, Meeta ; Sharma, Anil Kumar</creatorcontrib><description>X chromosomal short tandem repeats have the potential to complement the analyses of the autosomal, Y chromosomal, and mitochondrial DNA markers in forensics and population genetics, and extensive research on X chromosomal markers is being carried out. In the present study, a decaplex for the co-amplification of ten X chromosomal microsatellite loci (DXS6807, DXS8378, DXS7132, DXS6809, DXS6789, DXS101, DXS7133, GATA172D05, HPRTB, and GATA31E08) was optimized and 749 blood samples of unrelated male individuals from the four major linguistic families of India were analyzed. The number of alleles for the studied loci ranged from 7–16 while the gene diversity values varied from 0.408 to 0.855. Two new alleles were observed for the loci DXS101 and HPRTB. Statistical parameters of forensic interest were calculated and all loci were found to be polymorphic. High power of discrimination was observed for the loci DXS101, DXS6809, and DXS6789. The present study demonstrates the efficacy of these X-linked markers for human identification and kinship analysis.</description><identifier>ISSN: 0937-9827</identifier><identifier>EISSN: 1437-1596</identifier><identifier>DOI: 10.1007/s00414-010-0456-2</identifier><identifier>PMID: 20422205</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Biodiversity ; Chromosomes, Human, X ; DNA Fingerprinting ; Ethnic Groups - genetics ; Forensic Medicine ; Forensic sciences ; Gene Frequency ; Genetic Variation ; Genetics, Population ; Genotype ; Humans ; India ; Linguistics ; Male ; Medical Law ; Medicine ; Medicine & Public Health ; Mitochondrial DNA ; Polymerase Chain Reaction ; Software ; Tandem Repeat Sequences ; Technical Note ; X chromosomes</subject><ispartof>International journal of legal medicine, 2010-07, Vol.124 (4), p.327-330</ispartof><rights>Springer-Verlag 2010</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c402t-e4cd3de8d4fab2e1d01c166ba04f0fe78a30febb4e7f90e83147ef585eb78f343</citedby><cites>FETCH-LOGICAL-c402t-e4cd3de8d4fab2e1d01c166ba04f0fe78a30febb4e7f90e83147ef585eb78f343</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/s00414-010-0456-2$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00414-010-0456-2$$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/20422205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukerjee, Sanjukta</creatorcontrib><creatorcontrib>Ghosh, Tania</creatorcontrib><creatorcontrib>Kalpana, D.</creatorcontrib><creatorcontrib>Mukherjee, Meeta</creatorcontrib><creatorcontrib>Sharma, Anil Kumar</creatorcontrib><title>Genetic variation of 10 X chromosomal STR loci in Indian population</title><title>International journal of legal medicine</title><addtitle>Int J Legal Med</addtitle><addtitle>Int J Legal Med</addtitle><description>X chromosomal short tandem repeats have the potential to complement the analyses of the autosomal, Y chromosomal, and mitochondrial DNA markers in forensics and population genetics, and extensive research on X chromosomal markers is being carried out. In the present study, a decaplex for the co-amplification of ten X chromosomal microsatellite loci (DXS6807, DXS8378, DXS7132, DXS6809, DXS6789, DXS101, DXS7133, GATA172D05, HPRTB, and GATA31E08) was optimized and 749 blood samples of unrelated male individuals from the four major linguistic families of India were analyzed. The number of alleles for the studied loci ranged from 7–16 while the gene diversity values varied from 0.408 to 0.855. Two new alleles were observed for the loci DXS101 and HPRTB. Statistical parameters of forensic interest were calculated and all loci were found to be polymorphic. High power of discrimination was observed for the loci DXS101, DXS6809, and DXS6789. The present study demonstrates the efficacy of these X-linked markers for human identification and kinship analysis.</description><subject>Biodiversity</subject><subject>Chromosomes, Human, X</subject><subject>DNA Fingerprinting</subject><subject>Ethnic Groups - genetics</subject><subject>Forensic Medicine</subject><subject>Forensic sciences</subject><subject>Gene Frequency</subject><subject>Genetic Variation</subject><subject>Genetics, Population</subject><subject>Genotype</subject><subject>Humans</subject><subject>India</subject><subject>Linguistics</subject><subject>Male</subject><subject>Medical Law</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mitochondrial DNA</subject><subject>Polymerase Chain Reaction</subject><subject>Software</subject><subject>Tandem Repeat Sequences</subject><subject>Technical Note</subject><subject>X chromosomes</subject><issn>0937-9827</issn><issn>1437-1596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNqFkVtLxDAQhYMoul5-gC8SfPGpOrk17aMsugqC4AV8C2k70UrbrMlW8N-bdb2AID7NwHznDDOHkH0GxwxAn0QAyWQGDDKQKs_4GpkwKXTGVJmvkwmUqS8LrrfIdozPAEznWm2SLQ6Scw5qQqYzHHDR1vTVhtYuWj9Q7ygD-kDrp-B7H31vO3p7d0M7X7e0Hejl0LR2oHM_H7sPxS7ZcLaLuPdZd8j9-dnd9CK7up5dTk-vsloCX2Qo60Y0WDTS2Yoja4DVLM8rC9KBQ11YkUpVSdSuBCwEkxqdKhRWunBCih1ytPKdB_8yYlyYvo01dp0d0I_RaKlKmY6E_0khBKiy0Ik8_EU--zEM6QyjQAJjmi_t2Aqqg48xoDPz0PY2vBkGZpmEWSVh0m6zTMLwpDn4NB6rHptvxdfrE8BXQEyj4RHDz-a_Xd8BYw-RiQ</recordid><startdate>20100701</startdate><enddate>20100701</enddate><creator>Mukerjee, Sanjukta</creator><creator>Ghosh, Tania</creator><creator>Kalpana, D.</creator><creator>Mukherjee, Meeta</creator><creator>Sharma, Anil Kumar</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>7TM</scope></search><sort><creationdate>20100701</creationdate><title>Genetic variation of 10 X chromosomal STR loci in Indian population</title><author>Mukerjee, Sanjukta ; Ghosh, Tania ; Kalpana, D. ; Mukherjee, Meeta ; Sharma, Anil Kumar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-e4cd3de8d4fab2e1d01c166ba04f0fe78a30febb4e7f90e83147ef585eb78f343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biodiversity</topic><topic>Chromosomes, Human, X</topic><topic>DNA Fingerprinting</topic><topic>Ethnic Groups - genetics</topic><topic>Forensic Medicine</topic><topic>Forensic sciences</topic><topic>Gene Frequency</topic><topic>Genetic Variation</topic><topic>Genetics, Population</topic><topic>Genotype</topic><topic>Humans</topic><topic>India</topic><topic>Linguistics</topic><topic>Male</topic><topic>Medical Law</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mitochondrial DNA</topic><topic>Polymerase Chain Reaction</topic><topic>Software</topic><topic>Tandem Repeat Sequences</topic><topic>Technical Note</topic><topic>X chromosomes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukerjee, Sanjukta</creatorcontrib><creatorcontrib>Ghosh, Tania</creatorcontrib><creatorcontrib>Kalpana, D.</creatorcontrib><creatorcontrib>Mukherjee, Meeta</creatorcontrib><creatorcontrib>Sharma, Anil Kumar</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>Nucleic Acids Abstracts</collection><jtitle>International journal of legal medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukerjee, Sanjukta</au><au>Ghosh, Tania</au><au>Kalpana, D.</au><au>Mukherjee, Meeta</au><au>Sharma, Anil Kumar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic variation of 10 X chromosomal STR loci in Indian population</atitle><jtitle>International journal of legal medicine</jtitle><stitle>Int J Legal Med</stitle><addtitle>Int J Legal Med</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>124</volume><issue>4</issue><spage>327</spage><epage>330</epage><pages>327-330</pages><issn>0937-9827</issn><eissn>1437-1596</eissn><abstract>X chromosomal short tandem repeats have the potential to complement the analyses of the autosomal, Y chromosomal, and mitochondrial DNA markers in forensics and population genetics, and extensive research on X chromosomal markers is being carried out. In the present study, a decaplex for the co-amplification of ten X chromosomal microsatellite loci (DXS6807, DXS8378, DXS7132, DXS6809, DXS6789, DXS101, DXS7133, GATA172D05, HPRTB, and GATA31E08) was optimized and 749 blood samples of unrelated male individuals from the four major linguistic families of India were analyzed. The number of alleles for the studied loci ranged from 7–16 while the gene diversity values varied from 0.408 to 0.855. Two new alleles were observed for the loci DXS101 and HPRTB. Statistical parameters of forensic interest were calculated and all loci were found to be polymorphic. High power of discrimination was observed for the loci DXS101, DXS6809, and DXS6789. The present study demonstrates the efficacy of these X-linked markers for human identification and kinship analysis.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>20422205</pmid><doi>10.1007/s00414-010-0456-2</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0937-9827 |
ispartof | International journal of legal medicine, 2010-07, Vol.124 (4), p.327-330 |
issn | 0937-9827 1437-1596 |
language | eng |
recordid | cdi_proquest_miscellaneous_745940010 |
source | MEDLINE; HeinOnline Law Journal Library; SpringerLink Journals - AutoHoldings |
subjects | Biodiversity Chromosomes, Human, X DNA Fingerprinting Ethnic Groups - genetics Forensic Medicine Forensic sciences Gene Frequency Genetic Variation Genetics, Population Genotype Humans India Linguistics Male Medical Law Medicine Medicine & Public Health Mitochondrial DNA Polymerase Chain Reaction Software Tandem Repeat Sequences Technical Note X chromosomes |
title | Genetic variation of 10 X chromosomal STR loci in Indian population |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T23%3A30%3A33IST&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=Genetic%20variation%20of%2010%20X%20chromosomal%20STR%20loci%20in%20Indian%20population&rft.jtitle=International%20journal%20of%20legal%20medicine&rft.au=Mukerjee,%20Sanjukta&rft.date=2010-07-01&rft.volume=124&rft.issue=4&rft.spage=327&rft.epage=330&rft.pages=327-330&rft.issn=0937-9827&rft.eissn=1437-1596&rft_id=info:doi/10.1007/s00414-010-0456-2&rft_dat=%3Cproquest_cross%3E733305987%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=504011720&rft_id=info:pmid/20422205&rfr_iscdi=true |