共 86 条
New applications and developments in the use of multiplex ligation-dependent probe amplification
被引:67
作者:

Kozlowski, Piotr
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机构:
Polish Acad Sci, Inst Bioorgan Chem, Canc Genet Lab, PL-61704 Poznan, Poland Polish Acad Sci, Inst Bioorgan Chem, Canc Genet Lab, PL-61704 Poznan, Poland

Jasinska, Anna J.
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机构:
Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA USA Polish Acad Sci, Inst Bioorgan Chem, Canc Genet Lab, PL-61704 Poznan, Poland

Kwiatkowski, David J.
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Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Translat Med,Dept Med, Boston, MA 02115 USA Polish Acad Sci, Inst Bioorgan Chem, Canc Genet Lab, PL-61704 Poznan, Poland
机构:
[1] Polish Acad Sci, Inst Bioorgan Chem, Canc Genet Lab, PL-61704 Poznan, Poland
[2] Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA USA
[3] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Translat Med,Dept Med, Boston, MA 02115 USA
关键词:
Copy number variation;
Expression profiling;
Multiplex ligation-dependent probe amplification;
Mutation detection;
Transgene genotyping;
D O I:
10.1002/elps.200800126
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Multiplex ligation-dependent probe amplification (MLPA) is a commonly used technique for determining relative DNA sequence dosage (or copy number) in a complex DNA sample. Originally MLPA was designed as a copy number analysis tool for detecting disease-causing genomic mutations and has been successfully applied in the testing and identification of hundreds of genomic mutations in numerous genes including DMD, BRCA1, NF1, and TSC2. More recently, several modifications of the original technique have been implemented. Arguably the most important enhancement of MLPA has been probe generation by chemical synthesis, enabling the facile creation of novel probe sets for any desired application. Other newer applications of MLPA include methylation status determination, copy number analysis in segmentally duplicated regions, expression profiling, and transgene genotyping. MLPA has a potential major role in the analysis of common copy number variation in genome-wide association analyses, which may be enhanced by future improvements to increase throughput and lower costs, such as array-MLPA.
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页码:4627 / 4636
页数:10
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