Multiple displacement amplification to create a long-lasting source of DNA for genetic studies

被引:83
作者
Lovmar, L [1 ]
Syvänen, AC [1 ]
机构
[1] Univ Uppsala Hosp, Res Dept 2, Dept Med Sci, SE-75185 Uppsala, Sweden
关键词
multiple displacement amplification; MDA; whole genome amplification; WGA; phi 29 DNA polymerase; genotyping; comparative genomic hybridization;
D O I
10.1002/humu.20341
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
In many situations there may not be sufficient DNA collected from patient or population cohorts to meet the requirements of genome-wide analysis of SNPs, genomic copy number polymorphisms, or acquired copy number alternations. When the amount of available DNA for genotype analysis is limited, high performance whole-genome amplification (WGA) represents a new development in genetic analysis. It is especially useful for analysis of DNA extracted from stored histology slides, tissue samples, buccal swabs, or blood stains collected on filter paper. The multiple displacement amplification (MDA) method, which relies on isothermal amplification using the DNA polymerase of the bacteriophage 029, is a recently developed technique for high performance WGA. This review addresses new trends in the technical performance of MDA and its applications to genetic analyses. The main challenge of WGA methods is to obtain balanced and faithful replication of all chromosomal regions without the loss of or preferential amplification of any genomic loci or allele. In multiple comparisons to other WGA methods, MDA appears to be most reliable for genotyping, with the most favorable call rates, best genomic coverage, and lowest amplification bias. Hum Mutat 27(7), 603-614, 2006. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:603 / 614
页数:12
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