Microarrays, deep sequencing and the true measure of the transcriptome

被引：338

作者：

Malone, John H. ^{[1
]}

Oliver, Brian ^{[1
]}

机构：

[1] NIDDK, Cellular & Dev Biol Lab, NIH, Bethesda, MD 20892 USA

来源：

BMC BIOLOGY | 2011年 / 9卷

关键词：

GENE-EXPRESSION MEASUREMENTS; RNA-SEQ EXPERIMENTS; DROSOPHILA-MELANOGASTER; HUMAN GENOME; PREDICTION; PLATFORMS; QUALITY; REPRODUCIBILITY; NORMALIZATION; ARRAYS;

D O I：

10.1186/1741-7007-9-34

中图分类号：

Q [生物科学];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

Microarrays first made the analysis of the transcriptome possible, and have produced much important information. Today, however, researchers are increasingly turning to direct high-throughput sequencing - RNA-Seq - which has considerable advantages for examining transcriptome fine structure - for example in the detection of allele-specific expression and splice junctions. In this article, we discuss the relative merits of the two techniques, the inherent biases in each, and whether all of the vast body of array work needs to be revisited using the newer technology. We conclude that microarrays remain useful and accurate tools for measuring expression levels, and RNA-Seq complements and extends microarray measurements.

引用

页数：9

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