B. W. Ying

STR data for the AmpFlSTR profiler plus from western China.

Blood samples were collected from unrelated individuals ofChinese Han ethnic group in Chengdu of China. DNA was ex-tracted using Chelex method (1). 0.5–2ng target DNA followedthe protocols described in the AmpFlSTR Cofiler user’s manual(PE Applied Biosystems), the exception was that the PCR vol-umewas25µL.ThesampleswereamplifiedusingGeneAmpPCRSystem 9700 (Applied Biosystems, Foster City, CA). DNA typ-ing was carried out on the ABI 3100 Genetic Analyzer (AppliedBiosystems). The amplified products were detected with the ABIPRISM 3100 Genetic Analyzer using the separation medium Per-formance Optimized Polymer (POP) 4

Polymorphism data of two STR loci DYS632 and DYS634 in a Chinese Han population.

Blood samples were collected from 100 unrelated healthy males of the Chinese Han ethnic group in Chengdu of China. DNA was extracted using the Chelex method (1). The allelic variation at the two Y-STR loci named as DYS632 and DYS634 were analyzed by PCR amplification system. PCR amplification conditions can be accessed at: http://www.legalmed.org/dna/DYS632.htm. The volume of PCR reaction for each locus was 37.5 μL. The PCR products were analyzed by horizontal non-denaturing polyacrylamide gel electrophoresis with discontinuous buffer system and visualized by silver staining (2). Alleles were designated according to the recommendation of the International Society of Forensic Genetics (3). The gene diversity, the haplotype diversity, and the standard errors of diversity were calculated in accordance with Hou’s method (4). The complete data can be accessed at: http://www.legalmed. org/dna/DYS632.htm.

Population Genetic Study of 15 STR Loci in a Chinese Population

POPULATION:  Chinese (n = 501).

Genetic variation for five short tandem repeat loci in a central China population sample

POPULATION: Chinese.

Distributions of Allelic Frequencies and Haplotypes of Two New STR Loci in a Chinese Han Population

Blood samples were collected from unrelated individuals of Chinese Han ethnic group in Chengdu of China. DNA was extracted using Chelex method (1). PCR amplification conditions can be accessed at http://www.legalmed.org/dna/d3s4014.htm. The PCR reaction volume for each locus was 37.5μL. The PCR products were analyzed by horizontal non-denaturing polyacrylamide gel electrophoresis with discontinuous buffer system and visualized by silver staining (2). Data of population genetics and forensic science were analyzed using POWERSTATS program (3). The genotype distribution was analyzed for Hardy-Weinberg equilibrium

Polymorphism of three STR loci in Chinese population.

Blood samples were collected from unrelated individuals of Chinese Han ethnic group in Chengdu of China. DNA was extracted using Chelex method (1). PCR amplification conditions can be accessed at http://www.legalmed.org/dna/D12S1064.htm. The volume of PCR reaction for each locus was 37.5 μL. The PCR products were analyzed by horizontal non-denaturing polyacrylamide gel electrophoresis with discontinuous buffer system and visualized by silver staining (2). Data of population genetics and

Population genetics of two STR loci D13S796 and DYS439 in a Chinese han population

Blood samples were collected from unrelated healthy individuals ofChineseHan ethnic group inChengdu of Sichuan.GenomicDNA samples were extracted using Chelex-100method (1). PCR amplification conditions can be accessed at http://www.legalmed.org/dna/ D13S796 and DYS439.htm. The volume of PCR reaction for each locus was 37.5 μL. The PCR products were analyzed by horizontal non-denaturing polyacrylamide gel electrophoresis with discontinuous buffer system and visualized by sliver staining (2). Data of population genetics and forensic science of the locus D13S796 was analyzed using POWERSTATS program (3). Data of population

Population genetics of three STR loci D19S591, D5S1462 and D3S2432 in a Chinese Han population.

Blood samples were collected from unrelated healthy individuals of Chinese Han ethnic group in Chengdu of Sichuan, China after informed consent. Genomic DNA samples were extracted using Chelex-100 method (1). PCR amplification conditions can be accessed at http://www.legalmed.org/dna/D19S591.htm., http:// www. legalmed.org/dna/D5S1462.htm. and http://www.legalmed. org/ dna/D3S2432.htm. The volume of PCR reaction for each locus was 37.5μL. The PCR products were analyzed by horizontal nondenaturing polyacrylamide gel electrophoresis with discontinuous buffer system and visualized by silver staining (2). Data of population genetics and forensic science of the locus D19S591, D5S1462, D3S2432 was analyzed using POWERSTATS program (3). The

Allelic Frequencies of Three X-Y Homologous STR Loci in Chinese Population

We have analyzed the distribution of allele frequencies at three X-Y homologous short tandem repeat (STR) loci (DXS9900, DXS9905, DXS9906) among individuals (n= 385) in Chengdu, China

Allele Frequencies for Two STR Loci D11S1977 and D22S444 in Chinese Population

Blood samples were collected from unrelated individuals of Chinese Han ethnic group in Chengdu of China. DNA was extracted using Chelex method (1). Reaction condition of PCR amplification can be accessed at http://www.legalmed.org/ dna/D11S1977.htm. The volume of PCR reaction for each locus was 37.5 µL. The PCR products were analyzed by horizontal non-denaturing polyacrylamide gel electrophoresis with discontinuous buffer system, and visualized by silver staining (2,3). Data of population genetics and forensic science were analyzed using POWERSTATS program (4). The genotype distribution was analyzed for Hardy-Weinberg equilibrium according to Hous method (5) and no deviation from Hardy-Weinberg equilibrium was observed. The complete data can be accessed at http://www.legalmed.org/dna/D11S1977.htm.