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Massively parallel sequencing of sex-chromosomal STRs in Saudi Arabia reveals patrilineage-associated sequence variants.
Forensic Sci Int Genet. 2020 11; 49:102402.FS

Abstract

Massively parallel sequencing (MPS) of forensic STRs has the potential to reveal additional allele diversity compared to conventional capillary electrophoresis (CE) typing strategies, but population studies are currently relatively few in number. The Verogen ForenSeq™ DNA Signature Prep Kit includes both Y-STRs and X-STRs among its targeted loci, and here we report the sequences of these loci, analysed using Verogen's ForenSeq™ Universal Analysis Software (UAS) v1.3 and STRait Razor v3.0, in a representative sample of 89 Saudi Arabian males. We identified 56 length variants (equivalent to CE alleles) and 75 repeat sequence sub-variants across the six X-STRs analysed; equivalent figures for the set of 24 Y-STRs were 147 and 192 respectively. We also observed two flanking sequence variants for the X-, and six for the Y-STRs. Recovery of sequence data and concordance with CE data (where available) across the tested loci was good, though rare flanking variation affected interpretation and allele calling at DYF387S1 and DXS7132. Examination of flanking sequences of the Y-STRs revealed five SNPs (L255, M4790, BY7692, Z16708 and S17543) previously shown to define specific haplogroups by Y-chromosome sequencing. These define Y-haplogroups in 62 % of our sample, a proportion that increases to 91 % when haplogroup-associated repeat-sequence motifs are also considered. A population-level comparison of the Saudi Arabian X-STRs with a global sample showed our dataset to be part of a large cluster of populations of West Eurasian and Middle Eastern origin.

Authors+Show Affiliations

Department of Genetics & Genome Biology, University of Leicester, University Road, Leicester, UK; Forensic Genetics Laboratory, General Administration of Criminal Evidence, Public Security, Ministry of Interior, Saudi Arabia.Department of Genetics & Genome Biology, University of Leicester, University Road, Leicester, UK. Electronic address: maj4@le.ac.uk.Department of Genetics & Genome Biology, University of Leicester, University Road, Leicester, UK. Electronic address: jw418@le.ac.uk.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

33035796

Citation

Khubrani, Yahya M., et al. "Massively Parallel Sequencing of Sex-chromosomal STRs in Saudi Arabia Reveals Patrilineage-associated Sequence Variants." Forensic Science International. Genetics, vol. 49, 2020, p. 102402.
Khubrani YM, Jobling MA, Wetton JH. Massively parallel sequencing of sex-chromosomal STRs in Saudi Arabia reveals patrilineage-associated sequence variants. Forensic Sci Int Genet. 2020;49:102402.
Khubrani, Y. M., Jobling, M. A., & Wetton, J. H. (2020). Massively parallel sequencing of sex-chromosomal STRs in Saudi Arabia reveals patrilineage-associated sequence variants. Forensic Science International. Genetics, 49, 102402. https://doi.org/10.1016/j.fsigen.2020.102402
Khubrani YM, Jobling MA, Wetton JH. Massively Parallel Sequencing of Sex-chromosomal STRs in Saudi Arabia Reveals Patrilineage-associated Sequence Variants. Forensic Sci Int Genet. 2020;49:102402. PubMed PMID: 33035796.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Massively parallel sequencing of sex-chromosomal STRs in Saudi Arabia reveals patrilineage-associated sequence variants. AU - Khubrani,Yahya M, AU - Jobling,Mark A, AU - Wetton,Jon H, Y1 - 2020/10/02/ PY - 2020/06/17/received PY - 2020/09/18/revised PY - 2020/09/27/accepted PY - 2020/10/10/pubmed PY - 2021/7/14/medline PY - 2020/10/9/entrez KW - HGDP KW - Haplogroup KW - Massively parallel sequencing (MPS) KW - Population structure KW - Saudi Arabia KW - X-STRs KW - Y-SNPs KW - Y-STRs SP - 102402 EP - 102402 JF - Forensic science international. Genetics JO - Forensic Sci Int Genet VL - 49 N2 - Massively parallel sequencing (MPS) of forensic STRs has the potential to reveal additional allele diversity compared to conventional capillary electrophoresis (CE) typing strategies, but population studies are currently relatively few in number. The Verogen ForenSeq™ DNA Signature Prep Kit includes both Y-STRs and X-STRs among its targeted loci, and here we report the sequences of these loci, analysed using Verogen's ForenSeq™ Universal Analysis Software (UAS) v1.3 and STRait Razor v3.0, in a representative sample of 89 Saudi Arabian males. We identified 56 length variants (equivalent to CE alleles) and 75 repeat sequence sub-variants across the six X-STRs analysed; equivalent figures for the set of 24 Y-STRs were 147 and 192 respectively. We also observed two flanking sequence variants for the X-, and six for the Y-STRs. Recovery of sequence data and concordance with CE data (where available) across the tested loci was good, though rare flanking variation affected interpretation and allele calling at DYF387S1 and DXS7132. Examination of flanking sequences of the Y-STRs revealed five SNPs (L255, M4790, BY7692, Z16708 and S17543) previously shown to define specific haplogroups by Y-chromosome sequencing. These define Y-haplogroups in 62 % of our sample, a proportion that increases to 91 % when haplogroup-associated repeat-sequence motifs are also considered. A population-level comparison of the Saudi Arabian X-STRs with a global sample showed our dataset to be part of a large cluster of populations of West Eurasian and Middle Eastern origin. SN - 1878-0326 UR - https://www.unboundmedicine.com/medline/citation/33035796/Massively_parallel_sequencing_of_sex_chromosomal_STRs_in_Saudi_Arabia_reveals_patrilineage_associated_sequence_variants_ DB - PRIME DP - Unbound Medicine ER -