ArticleInternational journal of legal medicine2012
Mutation analysis of 24 short tandem repeats in Chinese Han population.
Article in International journal of legal medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 42 citations in OpenAlex.
- Allele and Haplotype Diversity of 26 X-STR Loci in Four Nationality Populations from China.PloS one · 2013Trial
- Developmental validation of a six-dye Multi-InDels kit for personal identification and paternity testing of highly degraded DNA samples.International journal of legal medicine · 2026Article
- Forensic characteristics and genetic variations of Han Chinese population in Shenzhen revealed by 23 autosomal STRs.Frontiers in genetics · 2026Article
- Identification of the Remains of an Adult Using DNA from Their Deciduous Teeth as a Reference Sample.Medicina (Kaunas, Lithuania) · 2023Article
- Verification of a loss of heterozygosity at the D8S1179 locus in a paternity case by the MiSeq FGx system.International journal of legal medicine · 2023Article
- THE APPLICATION OF CELL-FREE FETAL DNA (cff-DNA) AND SIBLINGS DNA METHODS IN THE PROCESS OF PATERNITY TEST THROUGH CODIS STR LOCI (CSF1PO, THO1, TPOX, AND vWA).African journal of infectious diseases · 2022Article
- SIBLING PAIR ANALYSIS IN THE IDENTIFICATION PROCESS OF THE MADURESE POPULATION USING STR CODIS LOCI.African journal of infectious diseases · 2022Article
- Mutation analysis of 28 autosomal short tandem repeats in the Chinese Han population.Molecular biology reports · 2021Article
- Mutation analysis of 19 autosomal short tandem repeats in Chinese Han population from Shanghai.International journal of legal medicine · 2016Article
- Worldwide F(ST) estimates relative to five continental-scale populations.Annals of human genetics · 2014Article
- The new guidelines for paternity analysis in Germany-how many STR loci are necessary when investigating duo cases?International journal of legal medicine · 2013Article
- Assessment of application value of 19 autosomal short tandem repeat loci of GoldenEye 20A kit in forensic paternity testing.International journal of legal medicine · 2013Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Germline mutations of 24 short tandem repeat (STR) loci (TPOX, D3S1358, FGA, D5S818, CSF1PO, D7S820, D8S1179, TH01, vWA, D13S317, Penta E, D16S539, D18S51, Penta D, D21S11, D2S1772, D6S1043, D7S3048, D8S1132, D11S2368, D12S391, D13S325, D18S1364, and GATA198B05) were studied for 6,441 parent-child meioses taken from the paternity testing cases in Chinese Han population. In total, 195 mutations were identified at 22 of the 24 loci. Among them, 189 (96.92%) mutations were one step, five mutations (2.56%) were two step, and one mutation (0.51%) was three step. No mutation was found at the TH01 and TPOX loci. The overall mutation rate estimated was 0.0013 (95% CI 0.0011-0.0015), and the locus-specific mutation rate estimated ranged from 0 to 0.0034. There was a bias in the STR mutations that repeat gains were more common than losses (∼1.7:1). Mutation events in the male germline were more frequent than in the female germline (∼4.3:1). Furthermore, loci with a larger heterozygosity tended to have a higher mutation rate. Mutation in short alleles was biased towards expansion, whereas mutation in long alleles favored contraction. The long alleles have a higher allelic mutational probability than short alleles.
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