Genetic Fingerprinting Using Microsatellite Markers in a Multiplex PCR Reaction: A Compilation of Methodological Approaches from Primer Design to Detection Systems

Author(s):  
Jacqueline Krüger ◽  
Dorit Schleinitz
Author(s):  
Kobayashi T ◽  
Uchibori S ◽  
Tsuzukibashi O ◽  
Uezato C ◽  
Goto H ◽  
...  

2017 ◽  
Vol 16 (4) ◽  
Author(s):  
Mu Yeong Lee ◽  
Hea Chang Moon ◽  
Hey Sook Jeon ◽  
Eui Geun Song ◽  
Donggul Woo ◽  
...  

2013 ◽  
Vol 37 (4) ◽  
pp. 205-211
Author(s):  
Lee-Kung Kima ◽  
◽  
Chang-Min Parka ◽  
Sun-Ae Park ◽  
Seung-Chang Kim ◽  
...  

PLoS ONE ◽  
2014 ◽  
Vol 9 (12) ◽  
pp. e115501 ◽  
Author(s):  
Daniela Sint ◽  
Bettina Niederklapfer ◽  
Ruediger Kaufmann ◽  
Michael Traugott

2017 ◽  
Vol 63 (6) ◽  
pp. 1127-1140 ◽  
Author(s):  
Mulias Lian ◽  
Mingjue Zhao ◽  
Caroline G Lee ◽  
Samuel S Chong

Abstract BACKGROUND Preimplantation genetic diagnosis (PGD) of myotonic dystrophy type 1 (DM1) currently uses conventional PCR to detect nonexpanded dystrophia myotonica protein kinase (DMPK) alleles or triplet-primed PCR to detect the CTG-expanded alleles, coupled with analysis of linked microsatellite markers to increase diagnostic accuracy. We aimed to simplify the process of identification and selection of informative linked markers for application to DM1 PGD. METHODS An in silico search was performed to identify all markers within 1–1.5 Mb flanking the DMPK gene. Five previously known (D19S559, APOC2, D19S543, D19S112, and BV209569) and 7 novel (DM45050, DM45178, DM45209, DM45958, DM46513, DM46892, and DM47004.1) markers with potentially high heterozygosity values and polymorphism information content were selected and optimized in a single-tube multiplex PCR panel. RESULTS Analysis of 184 DNA samples of Chinese and Caucasian individuals (91 from unrelated, anonymized cord blood of Chinese babies born at the National University Hospital, Singapore, and 93 Caucasian DNA samples from the Human Variation Panel HD100CAU) confirmed the high polymorphism indices of all markers (polymorphism information content >0.5), with observed heterozygosity values ranging from 0.62–0.93. All individuals were heterozygous for at least 6 markers, with 99.5% of individuals heterozygous for at least 2 markers on either side of the DMPK CTG repeat. The dodecaplex marker assay was successfully validated on 42 single cells and 12 whole genome amplified single cells. CONCLUSIONS The DM1 multiplex PCR panel is suitable for use in DM1 PGD either as a standalone linkage-based assay or as a complement to DMPK CTG repeat expansion-mutation detection.


2012 ◽  
Vol 13 (1) ◽  
pp. 96-102 ◽  
Author(s):  
Shigeo Nakamura ◽  
Toshio Masuda ◽  
Atsushi Mochizuki ◽  
Kazuhiko Konishi ◽  
Susumu Tokumaru ◽  
...  
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