An overview of current microarray-based human globin gene mutation detection methods

被引:24
作者
Cremonesi, Laura
Ferrari, Maurizio
Giordano, Piero C.
Harteveld, Cornelis L.
Kleanthous, Marina
Papasavva, Thessalia
Patrinos, George P.
Traeger-Synodinos, Joanne
机构
[1] Erasmus Univ, Med Ctr, Fac Med & Hlth Sci, MGC Dept Cell Biol & Genet, NL-3000 CA Rotterdam, Netherlands
[2] Ist Sci San Raffaele, Genom Unit Diag Human Pathol, I-20132 Milan, Italy
[3] Univ Vita Salute San Raffaele, Milan, Italy
[4] Diag & Ric San Raffaele SpA, Milan, Italy
[5] Leiden Univ, Med Ctr, Hemaglobinopathies Lab, Leiden, Netherlands
[6] Cyprus Inst Neurol & Genet, Mol Genet Unit, Nicosia, Cyprus
[7] Univ Athens, Sch Med, GR-11527 Athens, Greece
关键词
microarray; globin genes; mutation detection; microelectronic microchip; arrayed primer extension (APEX); thalassochip; multiple ligation probe amplification (MLPA); resequencing;
D O I
10.1080/03630260701459366
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
The Panoply of human globin gene mutation detection methods could become significantly enriched with the advent of microarray-based genotyping platforms. The aim of this article is to provide an overview of the current medium and high-throughput microarray-based globin gene mutation detection platforms, namely the microelectronic array, the "thalassochip" arrayed primer extension (APEX) technology and the single base extension methods. This article also outlines an emerging method based on multiple ligation probe amplification (MLPA) and discusses the implications of customized solutions for resequencing of genomic loci in relation to molecular genetic testing of hemoglobinopathies.
引用
收藏
页码:289 / 311
页数:23
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