Current trends in microsatellite genotyping

被引:674
作者
Guichoux, E. [1 ,2 ,3 ]
Lagache, L. [1 ,2 ]
Wagner, S. [1 ,2 ,4 ]
Chaumeil, P. [1 ,2 ]
Leger, P. [1 ,2 ]
Lepais, O. [1 ,2 ,5 ]
Lepoittevin, C. [1 ,2 ]
Malausa, T. [6 ]
Revardel, E. [1 ,2 ]
Salin, F. [1 ,2 ]
Petit, R. J. [1 ,2 ]
机构
[1] INRA, UMR Biodivers Genes & Communities 1202, F-33610 Cestas, France
[2] Univ Bordeaux, Biodivers Genes & Communities UMR1202, F-33400 Talence, France
[3] Pernod Ricard Res Ctr, F-94000 Creteil, France
[4] Univ Bonn, Steinmann Inst, D-53115 Bonn, Germany
[5] Univ Stirling, Sch Biol & Environm Sci, Stirling FK9 4LA, Scotland
[6] INRA, UMR IBSV INRA UNSA CNRS 1301, F-06903 Sophia Antipolis, France
关键词
binning; high throughput; multiplexing; nextgen sequencing; quality control; SSR; POLYMERASE-CHAIN-REACTION; SINGLE-NUCLEOTIDE POLYMORPHISMS; SIMPLE SEQUENCE REPEATS; WIDE GENETIC DIVERSITY; SHORT TANDEM REPEATS; HIGH-THROUGHPUT; MULTIPLEX PCR; CAPILLARY-ELECTROPHORESIS; INTERNATIONAL SOCIETY; GENOMIC DISTRIBUTION;
D O I
10.1111/j.1755-0998.2011.03014.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microsatellites have been popular molecular markers ever since their advent in the late eighties. Despite growing competition from new genotyping and sequencing techniques, the use of these versatile and cost-effective markers continues to increase, boosted by successive technical advances. First, methods for multiplexing PCR have considerably improved over the last years, thereby decreasing genotyping costs and increasing throughput. Second, next-generation sequencing technologies allow the identification of large numbers of microsatellite loci at reduced cost in non-model species. As a consequence, more stringent selection of loci is possible, thereby further enhancing multiplex quality and efficiency. However, current practices are lagging behind. By surveying recently published population genetic studies relying on simple sequence repeats, we show that more than half of the studies lack appropriate quality controls and do not make use of multiplex PCR. To make the most of the latest technical developments, we outline the need for a well-established strategy including standardized high-throughput bench protocols and specific bioinformatic tools, from primer design to allele calling.
引用
收藏
页码:591 / 611
页数:21
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