Large Number Of Alleles Research Articles

Major Histocompatibility Complex Class II Genes Allele Diversity in Landlocked Seals.

The allelic diversity of exon 2 (DQB gene) and exon 3 (DRB gene) of major histocompatibility complex class II was studied for the first time in two species of the landlocked pinnipeds, Baikal (N = 79) and Caspian (N = 32) seals, and these were in compared with the widespread Arctic species, the ringed seal (N = 13). The analysis of the second exon comprising the antigen-binding region revealed high allelic diversity in all three species but the pattern of the diversity was the most specific for the Baikal seal. This species differs from the other two by the smallest number of alleles in the population, yet they have the largest number of alleles per individual and by the maximum similarity of individual genotypes. Presumably, this specificity is a consequence of the spatial and temporal homogeneity of the Lake Baikal environment. Analysis of the third exon encoding the conserved β2-domain showed that the Baikal seal differs by the greatest number of amino acid sequences per individual, while the Caspian seal has the lowest number of variants. A single variant of the β2-domain, the same as in the ringed seal, predominates in the Caspian seal, whereas in the Baikal seal the two other variants predominate. At the same time, three species-specific amino acid sequences were observed among minor variants in the Caspian seal, while only one was found in the Baikal seal. This fact may suggest a longer period of independent evolution in the Caspian seal compared to the Baikal seal.

Genome-Wide Analysis of the Risk Association for the Development of Paranoid Schizophrenia in Russians: Search for Genetic Markers in the 1q43 Chromosomal Region

Schizophrenia is a highly hereditary disorder. Genetic risk is associated with a large number of alleles, including common alleles with little effect that can be found in genome-wide association studies. The aim of this study was to study genetic risk factors for the development of schizophrenia in a genome-wide association analysis (GWAS) in Russians from the Republic of Bashkortostan. The studied sample consisted of 320 patients with paranoid schizophrenia and 402 healthy individuals. GWAS genotyping of DNA samples was carried out on the PsychChip biochip, which included 610,000 single nucleotide polymorphic variants (SNPs).

A study on the genetic diversity and subpopulation structure of three Bulgarian mountainous sheep breeds, based on genotyping of microsatellite markers

Traditional domestic breeds of domestic animals are part of the “living” wealth of the world, part of the disappearing biodiversity and a valuable local gene pool. Nowadays, they are increasingly included in the category of “rare and disappearing” breeds. Therefore, the purpose of this study was to reveal the genetic diversity and population structure of three Bulgarian mountainous sheep breeds (Rhodopean Tsigai, RT; Middle Rhodopean sheep, MRS; and Karakachan sheep, KS). A total of 113 unrelated individuals (two flocks of each breed) from different regions of the country were investigated based on 11 STR (short tandem repeat) markers. The obtained results showed a total of 116 alleles in the three sheep breeds. The mean number of alleles, effective number of alleles, and polymorphism information content (PIC) values per loci were 8.21, 4.72, and 0.79. The largest number of alleles were found in the population of MRS (9.18 ± 0.76), followed by RT (8.27 ± 0.64) and KS (7.18 ± 0.47). The largest polymorphism was found in INRA005 and INRA06 loci with 11 and 10 alleles, respectively, and the smallest polymorphic loci were noted for the locus McM042 and INRA172 with only 6 alleles. The observed heterozygosity showed the highest value in KS (0.79 ± 0.04), followed by RT (0.76 ± 0.02) and MRS (0.73 ± 0.04). The range of expected heterozygosity was from 0.77 ± 0.02 in MRS to 0.75 ± 0.03 in KS. The fixation index FST, estimated by analysis of molecular variance (AMOVA), was 0.2090, indicating moderate levels of genetic differentiation among the populations. The FST between the investigated breeds indicated a moderate value of 0.216, and the analysis of variance (ANOVA) data showed only 1% variation among the populations, whereas 99% was due to variation within breeds. The results by the STRUCTURE analysis revealed that all breeds were heterogeneous and formed three distinct clusters. The results of the genetic diversity and structure analysis of the investigated breeds provide useful information for assessing the genetic diversity of other Bulgarian autochthonous sheep breeds, serving as a cornerstone for designing effective conservation management strategies.

Genetic Variability in Lithuanian Black and White Cattle with Different Proportions of Holstein Bloodline

Background: Maintaining genetic variability in livestock is the important step towards developing appropriate management strategies. When considering crossing native Lithuanian Black and White cattle (BW) with Holsteins (HL), comprehensive knowledge of breed characteristics, including genetic diversity, is required. The aim of this study was to determine the genetic variability between Lithuanian Black and White and Holstein cattle breeds in relation to groups with different proportions of the Holstein bloodline. Methods: A total of 126 cattle samples were studied at 13 microsatellite loci to estimate genetic variability. Result: The largest number of alleles was detected in the BW cattle group with at least 50% Holstein blood. Private alleles were found in all cattle groups except the BW cattle group with a 83-90% Holstein bloodline. Principal coordinate analyses (PCoA) showed the separation of the HL group and other BW groups, as well as the individual that was pure-blooded Lithuanian Black and White. The results revealed further actions breeders should take to retain the required genotype of the native Lithuanian Black and White cattle breed.

Origin and persistence of polymorphism in loci targeted by disassortative preference: a general model.

The emergence and persistence of polymorphism within populations generally requires specific regimes of natural or sexual selection. Here, we develop a unified theoretical framework to explore how polymorphism at targeted loci can be generated and maintained by either disassortative mating choice or balancing selection due to, for example, heterozygote advantage. To this aim, we model the dynamics of alleles at a single locus A in a population of haploid individuals, where reproductive success depends on the combination of alleles carried by the parents at locus A. Our theoretical study of the model confirms that the conditions for the persistence of a given level of allelic polymorphism depend on the relative reproductive advantages among pairs of individuals. Interestingly, equilibria with unbalanced allelic frequencies were shown to emerge from successive introduction of mutants. We then investigate the role of the function linking allelic divergence to reproductive advantage on the evolutionary fate of alleles within the population. Our results highlight the significance of the shape of this function for both the number of alleles maintained and their level of genetic divergence. Large number of alleles are maintained with substantial replacement of alleles, when disassortative advantage slowly increases with allelic differentiation . In contrast, few highly differentiated alleles are predicted to be maintained when genetic differentiation has a strong effect on disassortative advantage. These opposite effects predicted by our model explain how disassortative mate choice may lead to various levels of allelic differentiation and polymorphism, and shed light on the effect of mate preferences on the persistence of balanced and unbalanced polymorphism in natural population.

Allele Diversity of the Major Histocompatibility Complex in the Common Hamster (Cricetus cricetus) in Urban and Rural Populations

Based on the results of targeted sequencing on the Illumina platform we compared the allelic diversity of exon 2 of the DRB gene in urban (city of Simferopol) and rural populations of the common hamster. The urban population significantly differs from the rural one in terms of the composition and diversity of gene alleles. For individuals living in the city, a larger number of alleles, higher values of haplotype and nucleotide diversity indices, and a smaller proportion of individuals with a homozygous genotype were noted. Both populations are characterized by a significant excess of non-synonymous substitutions over synonymous ones and almost every allele of a gene corresponds to a different amino acid sequence. However, the influence of positive selection on the diversity of variants of antigen-binding sites in the alleles of the DRB gene in urban conditions is much more pronounced. The data suggest that resistance of common hamsters living in specific and varied conditions of the urban environment to various kinds of pathogenic load is higher than in rural populations.

Major histocompatibility IIβ diversity and peptide-binding groove properties associated with red sea bream iridovirus resistance

Major histocompatibility complex (MHC) II genes are key factors in presenting antigens derived from extracellular pathogens to CD4+ T cells. These genes are known to be associated with disease resistance in livestock, including cultured fish species. Genome-wide linkage analysis of RSIV-resistant red sea bream has revealed that MHC IIβ is linked to the RSIV-resistant trait and was suggested as a probable candidate gene responsible for the resistant trait. In the present study, diversity of the MHC IIβ gene in wild and farmed red sea bream populations was evaluated by analysis of an intronic minisatellite locus, PmaMHC2b. Haplotypes of the βI domain of MHC IIβ were identified by cloning, and linkage of minisatellite polymorphisms with haplotype was confirmed in farmed populations. Large numbers of alleles were observed in the wild population (30), while the domesticated populations showed significantly lower values (13). Thirteen haplotypes of MHC IIβ were observed; most haplotypes possessed the unique PmaMHC2b allele, but some were present in more than one PmaMHC2b allele. Each haplotype possessed a distinct amino acid sequence with no synonymous mutations. Among 16 amino acid positions involved in peptide-binding grooves, four were monomorphic and 12 polymorphic. Several positions differed in the RSIV-resistant and RSIV-susceptible phenotypes: five in hydrophilic/hydrophobic character and five in polarity. These results provide insight applicable to broodstock management and contribute to understanding RSIV resistance.

Ukrainian Holstein cattle DNA polymorphism study

The aim of the research was to evaluate the genetic structure of Ukrainian Holstein cattle (n = 150) of the state enterprise Chayka (Kiev region, Ukraine) on the basis of the analysis of 12 microsatellite DNA loci and 3 QTL genes: k-casein (CSN3), prolactin (PRL), and fatty acid synthase (FASN). A total of 93 allelic variants were identified, and the largest number of alleles were found for TGLA53, TGLA122 and TGLA227 loci, the mean PIC = 0.693, and the heterozygosity index for all loci was 0.7314. The greatest number of effective alleles per locus were found for the BM1824 locus. Based on association analyses, complex genotypes were established for the three genes (CSN3, PRL, FASN). It was found that the AAPRL AACSN3 AAFASN genotype determined the highest milk yield (8351 kg / lactation) and the protein content in milk (3.10%), whereas the AAPRL ABCSN3 GGFASN genotype determined the highest level of fat content in milk (3.80%).

HLA diversity in the Russian population assessed by next generation sequencing

Next generation sequencing is used to determine full-length sequences of HLA genes at the 4-field (allelic) resolution. The study was aimed at determining frequency and diversity of HLA alleles in a cohort of blood donors from the Registry of the National Research Center for Hematology who design ated themselves as Russians (including some not routinely typed variations in HLA gene regions). The studied population consisted of 1510 donors. HLA typing was performed by next generation sequencing. Libraries were performed with AllType NGS Amplification Kits (One Lambda, USA) and sequenced using MiSeq (Illumina, USA). Data analysis used the TypeStream Visual Software V2.0.0.68 (One Lambda, USA) and IPD-IMGT/HLA database 3.40.0.1. Arlequin 3.5 software was used for estimation of allele and haplotype frequencies, deviation from Hardy-Weinberg equilibrium. 82 HLA-A, 156 HLA-В and 85 HLA-С alleles were identified with four-field resolution. 45 HLA-DRB1 and 18 HLA-DQB1 alleles were identified with 2-3-field resolution. Considerable HLA diversity was found among the donors self-designated as Russians: the population had large numbers of distinct alleles at each HLA gene, high percentage of alleles (25-32% of HLA class I) were revealed only once. Sufficient numbers of new alleles were registered which are absent in the IPD-IMGT/HLA database. Considerable allelic diversity in Russian population is due to low-incidence alleles. Despite this diversity, the majority of HLA alleles detected at each locus were common. Significant HLA diversity of the donors was connected with a large number of alleles with rare occurrence. The novel alleles identified in our study differed from the known alleles by single nucleotide substitutions. The most common alleles at the four-field level were as follows: A*02:01:01:01 (27.1%), C*07:02:01:03 (13.1%), A*03:01:01:01 (13.0%), B*07:02:01:01 (13.0%), A*01:01:01:01 (11.6%) and C*07:01:01:01/16 (10.4%). The HLA alleles, which are common for Russian populations, are not always common or well-documented alleles in present catalogues. The data obtained in this study may be used as a reference sample for estimation of HLA allele frequencies in Russian population, for proper frequency evaluation of specific alleles when searching donors for allogeneic hematopoietic stem cell transplantation, as well as for association studies between HLA alleles and different diseases, and for research in population genetics.

Allele-Specific Thresholds of Eluted Ligands for T-Cell Epitope Prediction

A common strategy for predicting candidate human leukocyte antigen class I T-cell epitopes is to use an affinity-based threshold of 500 nM. Although a 500 nM threshold across alleles effectively identifies most epitopes across alleles, findings showing that major histocompatibility complex repertoire sizes vary by allele indicate that using thresholds specific to individual alleles may improve epitope identification. In this work, we compare different strategies utilizing common and allele-specific thresholds to identify an optimal approach for T-cell epitope prediction. First, we confirmed previous observations that different human leukocyte antigen class I alleles correspond with varying repertoire sizes. Here, we define general and allele-specific thresholds that capture 80% of eluted ligands and a different set of thresholds associated with capturing 9-mer T-cell epitopes at 80% sensitivity. Our analysis revealed that allele-specific threshold performance was roughly equivalent to that of a common threshold when considering a relatively large number of alleles. However, when predicting epitopes for only a few alleles, the use of allele-specific thresholds would be preferable. Finally, we present here for public use a set of allele-specific thresholds that may be used to identify T-cell epitopes at 80% sensitivity.

Forensic parameters and mutation analysis of 23 short tandem repeat (PowerPlex® Fusion System) loci in Fujian Han Chinese population.

Kinship testing based on genetic markers has valuable practical applications. Short tandem repeat polymorphisms (STRPs) can have large number of alleles, and become the dominant marker for kinship identification. However, the high mutation rates affect the identification accuracy. Thus, accurate investigation of the mutation rate of STR loci in different populations is crucial for the reliability of phylogenetic relationships. In present study, forensic parameters and mutation rates (include 95% CI) of 23 short tandem repeats (STR) loci (D3S1358, D1S1656, D2S441, D10S1248, D13S317, D16S539, D18S51, D2S1338, CSF1PO, TH01, vWA, D21S11, D7S820, D5S818, TPOX, D8S1179, D12S391, D19S433, FGA, D22S1045, PentaE, PentaD and DYS391) were investigated through PowerPlex® Fusion System in Fujian Han population. The high level of CDP (0.999999999999999999999999992) and CPE (0.999999993) indicated the panel was high efficiency in forensic DNA identification and paternity testing. In mutation analysis, 43 mutation cases were found through 54,124 parent-child meiotic transfers. The observed mutation rates ranged from 0 (D3S1358, D1S1656, D13S317, TH01, D19S433 and D22S1045) to 0.0025 (PentaE and FGA). The overall mutation rate across all loci was 0.0008 and the average mutation rate for the 23 loci was estimated to be 0.00078 per meiosis. The vast majority of mutations were single-step (88.4%) mutation and also include double-step (9.3%) and triple-step (2.3%) mutations. Paternal mutation rate was more common than maternal mutation rate with a ratio of 7.2:1. In addition, mutation rates indicated positive correlation (r = 0.633, p = 0.009) with the expected heterozygosity (He).

Diversidad genética de <i>Moniliophthora roreri</i> mediante Polimorfismo de Longitud de Fragmentos Amplificados (AFLPs)

El cultivo de cacao, está afectado por el fitopatógeno Moniliophthora roreri, que causa gran pérdida en la producción en Norte de Santander. Este estudio muestra los resultados obtenidos utilizando AFLPs de M. roreri. Con el kit para sistema de análisis II, estandarizado y aplicado a 56 muestras de M. roreri, aisladas de nueve municipios. La combinación que presentó mayor número de polimorfismos fue E-ACC/ M-CAA, con 100 bandas y un número menor de alelos (6), con la combinación E-ACG/ M-CAA se obtuvieron 90 bandas y un número de alelos mayor (23), y con la combinación E-AAC/ M-CAA se presentaron 94 bandas y alelos (12). El análisis de datos se realizó según el dendrograma de similitud o distancias genéticas de Nei, obteniéndose cinco grupos con una alta variabilidad entre las muestras, del 6,5 al 58%. Al combinar la información morfológica y molecular se determinó el nivel de diversidad genética de Moniliophthora roreri.

Allele frequencies in Azuay Population in Ecuador.

One hundred and eighty-two samples of unrelated people who requested the paternity test at the Molecular Biology and Genetics Laboratory of the Catholic University of Cuenca-Ecuador in the province of Azuay were studied, except for the D1S1656 (180 samples) and SE33 (89 samples) markers. The STRs D22S1045, D3S1358, VWA, D16S539, D2S1338, D8S1179, D21S11, D18S51, D19S433, TH01, FGA, D1S1656, D12S391, D10S1248, D2S441, and SE33 were typed from blood samples, amplifying the DNA by polymerase chain reactions and electrophoresis. The allele frequencies were estimated by simple counting and the impartial heterozygosity was also calculated. The Hardy-Weinberg equilibrium theory was studied. In the results obtained with the analyzed markers, the largest number of alleles can be observed in the markers with the highest polymorphic information content (PIC): D21S11, D16S539, D2S1338, D19S433, D18S51, FGA, D1S1656, and D12S391. In addition, SE33 was analyzed in certain samples, showing as result a high PIC, in fact, the highest one because of its great polymorphisc characteristic. Likewise, these markers are the ones providing the highest probability of discrimination and the lowest probability of coincidence.

The genetic architecture of the MHC class II region in British Texel sheep

Understanding the structure of the major histocompatibility complex, especially the number and frequency of alleles, loci and haplotypes, is crucial for efficient investigation of the way in which the MHC influences susceptibility to disease. Nematode infection is one of the most important diseases suffered by sheep, and the class II region has been repeatedly associated with differences in susceptibility and resistance to infection. Texel sheep are widely used in many different countries and are relatively resistant to infection. This study determined the number and frequency of MHC class II genes in a small flock of Texel sheep. There were 18 alleles at DRB1, 9 alleles at DQA1, 13 alleles at DQB1, 8 alleles at DQA2 and 16 alleles at DQB2. Several haplotypes had no detectable gene products at DQA1, DQB1 or DQB2, and these were defined as null alleles. Despite the large numbers of alleles, there were only 21 distinct haplotypes in the population. The relatively small number of observed haplotypes will simplify finding disease associations because common haplotypes provide more statistical power but complicate the discrimination of causative mutations from linked marker loci.

A Comparative Study of the Molecular Characteristics of Familial Gliomas and Other Cancers.

Familial cancers are those that co-occur among first-degree relatives without showing Mendelian patterns of inheritance. In this analysis, we compare the genomic characteristics of familial and sporadic cancers, with a focus on low-grade gliomas (LGGs) using sequence and expression data from the Cancer Genome Atlas. Familial cancers show similar genomic and molecular biomarker profiles to sporadic cancers, consistent with the similarity in their clinical features. There are no statistically significant differences among somatic mutation, copy number variant, or gene expression patterns between familial and sporadic cancers; methylation profiles are the only class of molecular data to show significant differences. Familial cancers are likely driven by multiple, individually weak contributions to familiality (i.e. large numbers of alleles and/or shared environmental risks). Consequently, these risk factors tend to be obscured by stronger confounding variables such as clinical or molecular variation among cancer subtypes.

Development of SSR markers and genetic diversity analysis in enset (Ensete ventricosum (Welw.) Cheesman), an orphan food security crop from Southern Ethiopia.

BackgroundEnset (Ensete ventricosum (Welw.) Cheesman; Musaceae) is a multipurpose drought-tolerant food security crop with high conservation and improvement concern in Ethiopia, where it supplements the human calorie requirements of around 20 million people. The crop also has an enormous potential in other regions of Sub-Saharan Africa, where it is known only as a wild plant. Despite its potential, genetic and genomic studies supporting breeding programs and conservation efforts are very limited. Molecular methods would substantially improve current conventional approaches. Here we report the development of the first set of SSR markers from enset, their cross-transferability to Musa spp., and their application in genetic diversity, relationship and structure assessments in wild and cultivated enset germplasm.ResultsSSR markers specific to E. ventricosum were developed through pyrosequencing of an enriched genomic library. Primer pairs were designed for 217 microsatellites with a repeat size > 20 bp from 900 candidates. Primers were validated in parallel by in silico and in vitro PCR approaches. A total of 67 primer pairs successfully amplified specific loci and 59 showed polymorphism. A subset of 34 polymorphic SSR markers were used to study 70 both wild and cultivated enset accessions. A large number of alleles were detected along with a moderate to high level of genetic diversity. AMOVA revealed that intra-population allelic variations contributed more to genetic diversity than inter-population variations. UPGMA based phylogenetic analysis and Discriminant Analysis of Principal Components show that wild enset is clearly separated from cultivated enset and is more closely related to the out-group Musa spp. No cluster pattern associated with the geographical regions, where this crop is grown, was observed for enset landraces. Our results reaffirm the long tradition of extensive seed-sucker exchange between enset cultivating communities in Southern Ethiopia.ConclusionThe first set of genomic SSR markers were developed in enset. A large proportion of these markers were polymorphic and some were also transferable to related species of the genus Musa. This study demonstrated the usefulness of the markers in assessing genetic diversity and structure in enset germplasm, and provides potentially useful information for developing conservation and breeding strategies in enset.Electronic supplementary materialThe online version of this article (doi:10.1186/s12863-015-0250-8) contains supplementary material, which is available to authorized users.

Biological insights from 108 schizophrenia-associated genetic loci.

SummarySchizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be detected by genome-wide association studies. Here, we report a multi-stage schizophrenia genome-wide association study of up to 36,989 cases and 113,075 controls. We identify 128 independent associations spanning 108 conservatively defined loci that meet genome-wide significance, 83 of which have not been previously reported. Associations were enriched among genes expressed in brain providing biological plausibility for the findings. Many findings have the potential to provide entirely novel insights into aetiology, but associations at DRD2 and multiple genes involved in glutamatergic neurotransmission highlight molecules of known and potential therapeutic relevance to schizophrenia, and are consistent with leading pathophysiological hypotheses. Independent of genes expressed in brain, associations were enriched among genes expressed in tissues that play important roles in immunity, providing support for the hypothesized link between the immune system and schizophrenia.

CONTRIBUTION OF WESTERN AND EASTERN SPECIES TO THE IRANIAN PEAR GERMPLASM REVEALED BY THE CHARACTERIZATION OF S-GENOTYPES

CONTRIBUTION OF WESTERN AND EASTERN SPECIES TO THE IRANIAN PEAR GERMPLASM REVEALED BY THE CHARACTERIZATION OF S-GENOTYPES

Genetic characterization and population bottleneck in the Hucul horse based on microsatellite and mitochondrial data

The aim of this work was to gather information about the origin and genetic characterization of the Central European Hucul horse based on 71 horses using 17 microsatellites and the D-loop region of mtDNA. Their genetic relationship to the Polish Konik (N = 7), German (N = 4) and Hungarian wild Przewalski horses (N = 4) and 200 horse sequences from GenBank was also analysed. Both microsatellite and mtDNA analysis showed a high genetic variation in the Hucul. A total of 130 alleles were detected, the mean number of observed alleles per microsatellite was 7.647, and the number of effective alleles was 4.401. The average observed and expected heterozygosity were 0.706 and 0.747, respectively. The high heterozygosity values and Wright's fixation index (FIS) (−0.128) indicated a low level of inbreeding, low or no selection pressure, and large number of alleles. mtDNA analysis revealed 18 haplotypes for the Hucul population with a total of 23 variable sites. Haplotype and nucleotide diversities were 0.935 ± 0.011 and 0.022 ± 0.012, respectively. Neutrality tests (Tajima's D and Fu's Fs) were non-significant, and mismatch distribution was ragged, indicating that the Hucul population is in genetic equilibrium. The most frequent mtDNA D-loop region belonged to haplogroup A (48%), which was also present in Przewalski Wild horse samples, while Polish Konik samples belonged to three haplotypes and C, F, and G haplogroups. Large and significant pairwise ΦST values along with a small number of common haplotypes indicated a low level of gene flow and lack of genetic structure among the three studied breeds (Hucul, Konik, and Przewalski Wild horse). The present work contributes to our knowledge of the genetic diversity of the Hucul horse and helps to define its genetic conservation. Biological Journal of the Linnean Society, 2013, 109, 54–65.

Genetic polymorphisms in 12 autosomal STRs in a Shanghai Han population from China

In this study, a total of 484 unrelated healthy individuals and 359 two-generation families in the Han population in Shanghai, China were successfully analyzed with the Investigator HDplex Kit (Qiagen, Hilden, Germany). Hardy-Weinberg equilibrium tests demonstrated no significant deviation from expected values (p > 0.05) for the 12 autosomal STRs included in this kit. A total of 173 alleles were detected in 12 autosomal STR loci; the largest number of alleles (32) was detected for the SE33 locus. The combined power of discrimination was 0.99999999992. The combined mean exclusion chance in duo cases was 0.99982, whereas the combined mean exclusion chance in trio cases was 0.9999986. The average mutation rate across all loci was 0.0023 (95% confidence intervals: 0.0013-0.0039). These results suggest that the 12 autosomal STR loci can provide highly informative polymorphic data for paternity testing and forensic identification in the Han population in Shanghai, China.