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1.
PLoS One ; 18(11): e0294973, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-38011210

RESUMO

A database for the Iraqi Sorani Kurds, specifically focused on the 12 X-short tandem repeat (STR) loci, has been developed to fascilitate forensic and population genetics investigations. The present study involved genotyping 117 unrelated individuals from the Sorani Kurds ethnic group using the Investigator Argus X-12 QS kit. The analysis revealed that the DXS10135 locus exhibited the highest degree of polymorphism, as indicated by a polymorphism information content (PIC) value of 0.94565 and a gene diversity (GD) value of 0.95623. Conversely, the DXS8378 locus displayed the lowest level of polymorphism, with a PIC value of 0.61026 and a GD value of 0.68170. Notably, two individuals were found to possess a rare allele (allele = 6) at the DXS8378 locus, which was not included in the allelic ladder of the kit. Furthermore, a significant linkage disequilibrium (LD) (p < 0.05/117) was observed between the DXS10103 and DXS10101 loci on linkage group 3 (LG3). The ancestral composition of the five primary geographic regions, namely Africa, Middle East, East Asia, Europe, and South America, was determined through the utilization of the [Formula: see text] ratio. The findings of this analysis revealed that the Middle Eastern populations exhibited the lowest [Formula: see text] ratio, measuring at 0.23243, indicating a relatively lower ancestral diversity. Conversely, the European populations showcased the highest [Formula: see text] ratio, measuring at 0.27122, indicative of a greater ancestral diversity within this region. Additionally, the allelic richness indicators, namely distinctive and private alleles, indicated that Africa and the Middle East displayed the highest levels, while Far East Asia exhibited the lowest. This analysis supports the hypothesis of repeated founder effects during outward migrations, as evidenced by both the ancestry variability and the allelic richness. Consequently, the findings of this study have important implications for forensic genetics and population genetics research, particularly in relation to the consideration of genetic predispositions within specific ethnic groups.


Assuntos
Cromossomos Humanos X , Genética Populacional , Humanos , Iraque , Polimorfismo Genético , Repetições de Microssatélites/genética , Impressões Digitais de DNA , Frequência do Gene
2.
PLoS One ; 18(9): e0290844, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37656680

RESUMO

The Y-chromosome has been widely used in forensic genetic applications and human population genetic studies due to its uniparental origins. A large database on the Qatari population was created for comparison with other databases from the Arabian Peninsula, the Middle East, and Africa. We provide a study of 23 Y-STR loci included in PowerPlex Y23 (Promega, USA) that were genotyped to produce haplotypes in 379 unrelated males from Qatar, a country at the crossroads of migration patterns. Overall, the most polymorphic locus provided by the Promega kit was DYS458, with a genetic diversity value of 0.85 and a haplotype diversity of 0.998924. Athey's Haplogroup Predictor tool was used to predict haplogroups from Y-STR haplotypes in the Qatari population. In a median-joining network, the haplogroup J1 predominance (49%) in Qatar generated a star-like expansion cluster. The graph of population Q-matrix was developed using Y-STR data from 38 Middle Eastern and 97 African populations (11,305 individuals), and it demonstrated a stronger sub-grouping of countries within each ethnic group and showed the effect of Arabs on the indigenous Berbers of North Africa. The estimated migration rate between the Qatari and other Arabian populations was inferred using Bayesian coalescence theory in the Migrate-n program. According to the Gene Flow study, the main migration route was from Yemen to Kuwait through Qatar. Our research, using the PowerPlex Y23 database, shows the importance of gene diversity, as well as regional and social structuring, in determining the utility of demographic and forensic databases.


Assuntos
Fluxo Gênico , Cromossomo Y , Masculino , Humanos , Teorema de Bayes , Arábia , Etnicidade
3.
J Forensic Leg Med ; 98: 102579, 2023 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-37619303

RESUMO

BACKGROUND: The study of hymen morphology and injuries is critical in forensic medicine, particularly in Iraq and other Asian countries. Problems with the hymen can have serious social consequences. AIM OF THE STUDY: The aim of this study is to shed light on various hymen's variants, as well as the possible causes of their injuries and their medicolegal significance. METHOD: This study was carried out at Baghdad's medico-legal directorate (M.L.D.) from January 1st to March 31st, 2017. There were 127 cases in total. They ranged in age from two to sixty. The morphology of the hymens, their injuries, and other relevant details were documented using a specific questionnaire. RESULTS: Compared to other varied examinations undertaken, such as infertility, impotence, and others, the examination of the hymen made up (5.1%) of all examinations conducted in the Medico-Legal Directorate (M.L.D.) clinic in Baghdad. The majority of the women tested were over the age of 14. The annular hymen was the most common variant (57.3%). The elastic hymens percentage was 14.6% while the Imperforated variant had the lowest prevalence (0.8%). The majority of the properties of the examined hymens were smooth free edge, medium consistency, and medium sized hymen opening. The majority of the cases involved female children (prepubertal girls) who were accidently injured, followed by sexual assaults and wedding night doubts. The majority of hymen tears (40.2%) were old. Multiple tears (47.5%) outnumbered single tears (37.3%). Fresh tears were only observed in adult girls. CONCLUSION: The annular variant of the smooth free edge, average consistency, and average hole size is the most common hymens. The elastic hymens were a main reason for the referral of cases for medical examination due to wedding night doubts. In more than half of the cases, the hymens were smooth with no transection or deep notches.


Assuntos
Disfunção Erétil , Hímen , Adulto , Criança , Masculino , Humanos , Feminino , Instituições de Assistência Ambulatorial , Ásia , Emoções
4.
BMC Genomics ; 23(1): 763, 2022 Nov 21.
Artigo em Inglês | MEDLINE | ID: mdl-36414939

RESUMO

BACKGROUND: The Kurds as an ethnic group are believed to be a combination of earlier Indo-European tribes who migrated and inhabited a mountainous area thousands of years ago. However, as it is difficult to describe the precise history of their origin, it is necessary to investigate their population relationship with other geographical and ethnic groups. RESULTS: Seventeen Short Tandem Repeat markers on the Y chromosome (Y-STR) included in the AmpFLSTR™ Yfiler™ PCR Amplification Kit (Thermo Fisher Scientific, USA) were used to type DNA samples from the Sorani (Central) Kurdish population in Sulaymaniyah province. One hundred fifty-seven haplotypes were obtained from 162 unrelated male individuals. The highest and lowest gene diversities were DYS385a/b (GD = 0.848) and DYS392 (GD = 0.392), respectively. The haplotypes were used to predict the most likely haplogroups in the Sulaymaniyah population. CONCLUSION: Haplogroup prediction indicated predominance (28%) of subclade J2 (44/157) in the Sorani Kurds, northeast of Iraq. The pairwise genetic distance results showed that the Kurdish group clustered along with Asian populations, whereas the furthest countries were Europeans and Africans.


Assuntos
Cromossomos Humanos Y , Polimorfismo Genético , Masculino , Humanos , Cromossomos Humanos Y/genética , Frequência do Gene , Iraque , Genética Populacional
5.
Genes (Basel) ; 13(3)2022 03 17.
Artigo em Inglês | MEDLINE | ID: mdl-35328085

RESUMO

Gypsies are a separate ethnic group living in Pakistan and some other countries as well. They are mostly known as 'Roma' and 'untouchables'. They have different types of lifestyles as compared to other common people, as they always keep migrating from one place to another. They do not have proper houses; they live in tent houses and most probably work on daily wages to earn their living. Gypsies cannot be specified according to the place of residence and can only be classified according to their migration route. Previous historical and linguistic research showed the north Indian origin of Roma people. The present study collected 285 unrelated Roma individuals living in Punjab and typed with the Goldeneye Y20 system. Allelic frequencies ranged between 0.0035 and 0.5266, with haplotype diversity (HD) of 0.9999 and discrimination capacity (DC) of 0.8790. Gene diversity (GD) ranged from 0.6489 (DYS391) to 0.9764 (DYS391) (DY385ab). A total of 223 unique alleles were observed. Interestingly, the haplogroup R accounted for 40.56% and J for 22.06%. In MDS analysis, Pakistani Roma formed a close cluster with Roma from Constanta, Romania. The migration pattern of the Roma population from Pakistan, India and Europe was inferred using coalescence theory in the Migrate-n program. Overlapping Y-STR data were used to test different migration models. These migration models showed us the dominant gene flow from Pakistan to India and Europe to Pakistan. The results of our study showed that Y STRs provided substantially stronger discriminatory power in the Pakistani Roma population.


Assuntos
Cromossomos Humanos Y , Roma (Grupo Étnico) , Cromossomos Humanos Y/genética , Etnicidade/genética , Frequência do Gene , Haplótipos , Humanos , Masculino , Paquistão , Roma (Grupo Étnico)/genética
6.
Sci Rep ; 10(1): 15289, 2020 09 17.
Artigo em Inglês | MEDLINE | ID: mdl-32943725

RESUMO

Y-STRs have emerged as important forensic and population genetic markers for human identification and population differentiation studies. Therefore, population databases for these markers have been developed for almost all major populations around the world. The Iraqi population encompasses several ethnic groups that need to be genetically characterised and evaluated for possible substructures. Previous studies on the Iraqi population based on Y-STR markers were limited by a restricted number of markers. A larger database for Iraqi Arab population needed to be developed to help study and compare the population with other Middle Eastern populations. Twenty-three Y-STR loci included in the PowerPlex Y23 (Promega, Madison, WI, USA) were typed in 254 males from the Iraqi Arab population. Global and regional Y-STR analysis demonstrated regional genetic continuity among the populations of Iraq, the Arabian Peninsula and the Middle East. The Iraqi Arab haplotypes were used to allocate samples to their most likely haplogroups using Athey's Haplogroup Predictor tool. Prediction indicated predominance (36.6%) of haplogroup J1 in Iraqi Arabs. The migration rate between other populations and the Iraqis was inferred using coalescence theory in the Migrate-n program. Y-STR data were used to test different out-of-Africa migration models as well as more recent migrations within the Arabian Peninsula. The migration models demonstrated that gene flow to Iraq began from East Africa, with the Levantine corridor the most probable passageway out of Africa. The data presented here will enrich our understanding of genetic diversity in the region and introduce a PowerPlex Y23 database to the forensic community.


Assuntos
Árabes/genética , Cromossomos Humanos Y/genética , Fluxo Gênico/genética , África , Marcadores Genéticos/genética , Genética Populacional/métodos , Haplótipos/genética , Humanos , Iraque , Masculino , Repetições de Microssatélites/genética , Oriente Médio , População Branca/genética
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