Sequencing of human identification markers in an Uyghur population using the MiSeq FGx^(TM) Forensic Genomics System  

在线阅读下载全文

作  者:Halimureti Simayijiang Niels Morling Claus Børsting 

机构地区:[1]Faculty of Health and Medical Sciences,Section of Forensic Genetics,Department of Forensic Medicine,University of Copenhagen,Copenhagen,Denmark [2]Faculty of Criminal Science and Technology,Xinjiang Police College,Xinjiang,China

出  处:《Forensic Sciences Research》2022年第2期154-162,共9页法庭科学研究(英文)

摘  要:Massively parallel sequencing(MPS)offers a useful alternative to capillary electrophoresis(CE)based analysis of human identification markers in forensic genetics.By sequencing short tandem repeats(STRs)instead of determining the fragment lengths by CE,the sequence variation within the repeat region and the flanking regions may be identified.In this study,we typed 264 Uyghur individuals using the MiSeq FGx^(^(TM)) Forensic Genomics System and Primer Mix A of the ForenSeq^(^(TM)) DNA Signature Prep Kit that amplifies 27 autosomal STRs,25 Y-STRs,seven X-STRs,and 94 HID-SNPs.STRinNGS v.1.0 and GATK 3.6 were used to analyse the STR regions and HID-SNPs,respectively.Increased allelic diversity was observed for 33 STRs with the PCR-MPS assay.The largest increases were found in DYS389II and D12S391,where the numbers of sequenced alleles were 3–4 times larger than those of alleles determined by repeat length alone.A relatively large number of flanking region variants(28 SNPs and three InDels)were observed in the Uyghur population.Seventeen of the flanking region SNPs were rare,and 12 of these SNPs had no accession number in dbSNP.The combined mean match probability and typical paternity index based on 26 sequenced autosomal STRs were 3.85E36 and 1.49Eþ16,respectively.This was 10000 times lower and 1000 times higher,respectively,than the same parameters calculated from STR repeat lengths.

关 键 词:Forensic sciences forensic genetics massively parallel sequencing(MPS) short tandem repeat(STR) single nucleotide polymorphism(SNP) ForenSeq^(TM)DNA Signature Prep Kit UYGHUR 

分 类 号:D919[医药卫生—法医学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象