法庭科学DNA研究方案
阅微基因拥有一代测序、二代测序、qPCR 及基因芯片等平台,可以多方位对人源细胞、微生物等的STR、SNP、DNA 甲基化、Mt-DNA 进行单一 / 集成化的长度多态性或序列多态性等方面检测,获取从简单到复杂的遗传信息,为法医的研究提供更多的解决方案及简易的工作流程。
重要合作成果
1. Genetic distribution of 39 STR loci in 1027 unrelated Han individuals from Northern China. FSI: Genetics(影响因子:5.637)
2. Concurrent copy number variations on chromosome 8 and 22 combined with mutation at FGA locus revealed in a parentage testing case.FSI: Genetics(影响因子:5.637)
3. Genetic polymorphism of 22 autosomal STR markers in a Han population of Southern China. FSI: Genetics(影响因子:5.637)
4. Validation of the Microreader 23sp ID system: A new STR 23-plex system for forensic application. FSI: Genetics(影响因子:5.637)
5.A genomic audit of newly-adopted autosomal STRs for forensic identification. FSI: Genetics(影响因子:5.637)
6. Development of a rapid 21‐plex autosomal STR typing system for forensic applications. Electrophoresis(影响因子:2.569)
7. Inconsistent genotyping call at DYS389 locus and implications for interpretation. International Journal of Legal Medicine(影响因子:2.316)
8. Population data for 22 autosomal STR loci in the Uygur ethnic minority
. International Journal of Legal Medicine(影响因子:2.316)
9. Forensic molecular genetic diversity analysis of Chinese Hui ethnic group based on a novel STR panel. International Journal of Legal Medicine(影响因子:2.316)