نتایج جستجو برای: d18s51
تعداد نتایج: 66 فیلتر نتایج به سال:
STR multiplexes have been indispensable for the efficient genotyping of forensic samples. The PowerPlex 16 System contains the coreCODIS loci, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, D21S11, CSF1PO, FGA, THOI, TPOX, vWA, the sex determinant locus, amelogenin, and two pentanucleotide STR loci, Penta D and Penta E. This multiplex satisfies the locus requirements for most natio...
BACKGROUND The Tibeto-Burman (TB) populations are one of the four major linguistic population groups of India. They are considered belonging to different stocks and show wide variation in culture and language; however, their genetic relationship, antiquity and migration history among the regional populations has been little investigated. Molecular genetic studies are expected to clearly show th...
The amplification and typing conditions for the 13 core CODIS loci and their forensic applicability were evaluated. These loci are CSF1PO, FGA, TH01, TPOX, vWA, D3S1358, D5S818, D7S820, D8S1179, D13S317, D16S539, D18S51, and D21S11. Results were obtained using the multiplex STR systems AmpFlSTR Profiler Plus and AmpFlSTR COfiler (Applied Biosystems, Foster City, CA), GenePrint PowerPlex (Promeg...
The Han Ethnic Group is the largest among the 56 ethnic groups in China, accounting for 92% of the total population. The Han people are found in all parts of the country. One study showed that the Han Chinese population was actually substructured in a complex manner, with the main observed clusters roughly corresponding to the Northern-Han, Central-Han, and SouthernHan populations [1]. In the p...
Short tandem repeat (STR) loci in the human genome can be used for individual identification (1). Simultaneous PCR-amplification and size determination at several STR loci is desirable in order to: (i) increase the information gained when only very small amounts of template DNA are available, (ii) maximise throughput of samples and (iii) minimise costs. One means of increasing the number of loc...
Embryonic chromosomal abnormalities are the major cause of miscarriage. An accurate, rapid, and cheap method chromosome analysis in miscarriage is warranted clinical practice. Thus, a high-throughput ligation-dependent probe amplification (HLPA)-based detecting aneuploidies copy number variations was developed. A total 1060 cases were assessed. Each specimen subjected to quantitative fluorescen...
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