Investigator Argus X-12 study on the population of northern Croatia

X chromosome STR typing has emerged recently as a powerful tool, complementary to autosomal STR typing, in solving complex forensic and missing person cases. Investigator® Argus X-12 is a commercial product that allows co-amplification of 12 X chromosomal markers belonging to four linkage groups (LG...

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Published in:Genetics and Molecular Biology
Main Authors: Crnjac, Josip, Ozretić, Petar, Merkaš, Siniša, Ratko, Martina, Lozančić, Mateja, Korolija, Marina, Popović, Maja, Mršić, Gordan
Format: Text
Language:English
Published: Sociedade Brasileira de Genética 2016
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409765/
http://www.ncbi.nlm.nih.gov/pubmed/27768154
https://doi.org/10.1590/1678-4685-GMB-2015-0261
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spelling ftpubmed:oai:pubmedcentral.nih.gov:5409765 2023-05-15T16:31:11+02:00 Investigator Argus X-12 study on the population of northern Croatia Crnjac, Josip Ozretić, Petar Merkaš, Siniša Ratko, Martina Lozančić, Mateja Korolija, Marina Popović, Maja Mršić, Gordan 2016-10-20 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409765/ http://www.ncbi.nlm.nih.gov/pubmed/27768154 https://doi.org/10.1590/1678-4685-GMB-2015-0261 en eng Sociedade Brasileira de Genética http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409765/ http://www.ncbi.nlm.nih.gov/pubmed/27768154 http://dx.doi.org/10.1590/1678-4685-GMB-2015-0261 Copyright © 2016, Sociedade Brasileira de Genética. http://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited. CC-BY Human and Medical Genetics Text 2016 ftpubmed https://doi.org/10.1590/1678-4685-GMB-2015-0261 2017-05-14T00:06:22Z X chromosome STR typing has emerged recently as a powerful tool, complementary to autosomal STR typing, in solving complex forensic and missing person cases. Investigator® Argus X-12 is a commercial product that allows co-amplification of 12 X chromosomal markers belonging to four linkage groups (LGs). In this study, we analyzed by capillary electrophoresis blood samples from 100 females and 102 males from a population of northern Croatia. Statistical analysis included calculation of allele and haplotype frequencies, as well as forensic parameters. The most informative marker for the northern Croatia population was DXS10135 with PIC=0.9211 and a total of 27 alleles. The least polymorphic marker was DXS8378 with 6 alleles. The proportion of observed haplotypes from the number of possible haplotypes varied from 2.74–8.57% across all LGs, with LG1 being the most informative. Of the 11 tested world populations compared to the population of northern Croatia, significant differences in genetic distance (FST) were found for Greenlandic and all non-European populations. We found that all tested markers are in HWE and can thus be used for match probability calculation. Because of high combined power of discrimination in both men and women, Investigator® Argus X-12 is applicable for the northern Croatia population in routine forensic casework. Text greenlandic PubMed Central (PMC) Genetics and Molecular Biology 40 1 80 83
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Human and Medical Genetics
spellingShingle Human and Medical Genetics
Crnjac, Josip
Ozretić, Petar
Merkaš, Siniša
Ratko, Martina
Lozančić, Mateja
Korolija, Marina
Popović, Maja
Mršić, Gordan
Investigator Argus X-12 study on the population of northern Croatia
topic_facet Human and Medical Genetics
description X chromosome STR typing has emerged recently as a powerful tool, complementary to autosomal STR typing, in solving complex forensic and missing person cases. Investigator® Argus X-12 is a commercial product that allows co-amplification of 12 X chromosomal markers belonging to four linkage groups (LGs). In this study, we analyzed by capillary electrophoresis blood samples from 100 females and 102 males from a population of northern Croatia. Statistical analysis included calculation of allele and haplotype frequencies, as well as forensic parameters. The most informative marker for the northern Croatia population was DXS10135 with PIC=0.9211 and a total of 27 alleles. The least polymorphic marker was DXS8378 with 6 alleles. The proportion of observed haplotypes from the number of possible haplotypes varied from 2.74–8.57% across all LGs, with LG1 being the most informative. Of the 11 tested world populations compared to the population of northern Croatia, significant differences in genetic distance (FST) were found for Greenlandic and all non-European populations. We found that all tested markers are in HWE and can thus be used for match probability calculation. Because of high combined power of discrimination in both men and women, Investigator® Argus X-12 is applicable for the northern Croatia population in routine forensic casework.
format Text
author Crnjac, Josip
Ozretić, Petar
Merkaš, Siniša
Ratko, Martina
Lozančić, Mateja
Korolija, Marina
Popović, Maja
Mršić, Gordan
author_facet Crnjac, Josip
Ozretić, Petar
Merkaš, Siniša
Ratko, Martina
Lozančić, Mateja
Korolija, Marina
Popović, Maja
Mršić, Gordan
author_sort Crnjac, Josip
title Investigator Argus X-12 study on the population of northern Croatia
title_short Investigator Argus X-12 study on the population of northern Croatia
title_full Investigator Argus X-12 study on the population of northern Croatia
title_fullStr Investigator Argus X-12 study on the population of northern Croatia
title_full_unstemmed Investigator Argus X-12 study on the population of northern Croatia
title_sort investigator argus x-12 study on the population of northern croatia
publisher Sociedade Brasileira de Genética
publishDate 2016
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409765/
http://www.ncbi.nlm.nih.gov/pubmed/27768154
https://doi.org/10.1590/1678-4685-GMB-2015-0261
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op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409765/
http://www.ncbi.nlm.nih.gov/pubmed/27768154
http://dx.doi.org/10.1590/1678-4685-GMB-2015-0261
op_rights Copyright © 2016, Sociedade Brasileira de Genética.
http://creativecommons.org/licenses/by/4.0/
License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
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