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Your search keyword '"Han, Myun Soo"' showing total 29 results
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29 results on '"Han, Myun Soo"'

10. Forensic genetic analysis of mitochondrial DNA hypervariable region I/II sequences: An expanded Korean population database.

Author

Jin, Han Jun, Kwak, Kyoung Don, Hong, Seung Bum, Shin, Dong Jik, Han, Myun Soo, Tyler-Smith, Chris, and Kim, Wook

Subjects
Forensic genetics -- Research -- Analysis, Haplotypes -- Research -- Analysis, Human population genetics -- Research -- Analysis, Mitochondrial DNA -- Analysis -- Research
Abstract

Abstract We have analyzed variation of the mitochondrial DNA (mtDNA) hypervariable segments I and II (HVS-I and HVS-II) in 185 randomly chosen individuals from Korea to provide an expanded and [...]

Published
2006

11. Y-chromosome STR haplotype profiling in the Korean population.

Author

Kim, Yung Jin, Shin, Don Jik, Kim, Jung Min, Jin, Han Jun, Kwak, Kyoung Don, Han, Myun Soo, Choi, Sang Kyu, and Kim, Wook

Subjects
Y chromosome -- Analysis, Human population genetics -- Analysis, Forensic genetics -- Methods, Koreans -- Physiological aspects
Published
2001

22. Korean population genetic data for eleven STR loci.

Author

Han, Myun Soo, Kang, Pil Won, Choi, Dong Ho, Lee, Yang Han, Choi, Sang Kyu, Yoon, Song Ro, Shin, Dong Jik, Kim, Jung Min, Jin, Han Jun, Kwak, Kyoung Don, and Kim, Wook

Subjects
Forensic genetics -- Methods, Population genetics -- Research, Koreans -- Physiological aspects
Published
2001

29. Korean population genetic data and concordance for the PowerPlex® ESX 17, AmpFlSTR Identifiler®, and PowerPlex® 16 systems.

Author

Hong, Seung Beom, Kim, Soon Hee, Kim, Ki Cheol, Park, Moon Hee, Lee, Jeung Yoon, Song, Joon Myong, Han, Myun Soo, and Kim, Wook

Subjects
POPULATION genetics, INVESTIGATIONS, TANDEM repeats, PATERNITY testing, MOTHERHOOD, GENETIC mutation, FORENSIC genetics
Abstract

In case of paternity or maternity investigations with short tandem repeat (STR) analysis, deficient cases, missing person, or mutations are encountered and common STRs cannot provide sufficient forensic parameters. Thus, it is recommended that additional STRs are needed to complement conventional analysis for more reliable forensic information. We analyzed variation of 23 STRs contained in the new PowerPlex® ESX 17 kit (Promega) and two conventional kits of the AmpFlSTR Identifiler® (Applied Biosystems) and PowerPlex® 16 systems (Promega) in 452 randomly chosen individuals from Korea to provide an expanded and reliable Korean database. Allele frequencies and forensic parameters were used to evaluate suitability and robustness of the new kit for forensic genetic analysis as well as in concordance studies. The combined probability of match for the 16 loci in the PowerPlex® ESX 17 system was 2.76×10−20. One genotyping discrepancy due to a null allele was observed at the D18S51 locus (the concordant rate=99.99%), showing a primer-binding site mutation in the sequence of the locus (G-to-A substitution at position 146 of Genbank accession number JX018211). Thus, the new kit is a valuable forensic tool and is suitable to extend the Korean population genetic data obtained with well-established polymerase chain reaction multiplex-kits of the AmpFlSTR Identifiler® and PowerPlex® 16 systems. [ABSTRACT FROM AUTHOR]

Published
2013
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