Measuring differential gene expression by short read sequencing: quantitative comparison to 2-channel gene expression microarrays

• Main Authors: Kruglyak Leonid, Khan Zia, Bloom Joshua S, Singh Mona, Caudy Amy A
• Format: Article
• Language: English
• Published: BMC 2009-05-01
• Series: BMC Genomics
• Online Access: http://www.biomedcentral.com/1471-2164/10/221

<p>Abstract</p> <p>Background</p> <p>High-throughput cDNA synthesis and sequencing of poly(A)-enriched RNA is rapidly emerging as a technology competing to replace microarrays as a quantitative platform for measuring gene expression.</p> <p>Results</p> <p>Consequently, we compared full length cDNA sequencing to 2-channel gene expression microarrays in the context of measuring differential gene expression. Because of its comparable cost to a gene expression microarray, our study focused on the data obtainable from a single lane of an Illumina 1 G sequencer. We compared sequencing data to a highly replicated microarray experiment profiling two divergent strains of <it>S. cerevisiae</it>.</p> <p>Conclusion</p> <p>Using a large number of quantitative PCR (qPCR) assays, more than previous studies, we found that neither technology is decisively better at measuring differential gene expression. Further, we report sequencing results from a diploid hybrid of two strains of <it>S. cerevisiae </it>that indicate full length cDNA sequencing can discover heterozygosity and measure quantitative allele-specific expression simultaneously.</p>