Title | Measuring differential gene expression by short read sequencing: quantitative comparison to 2-channel gene expression microarrays. |
Publication Type | Journal Article |
Year of Publication | 2009 |
Authors | Bloom, JS, Khan, Z, Kruglyak, L, Singh, M, Caudy, AA |
Journal | BMC Genomics |
Volume | 10 |
Pagination | 221 |
Date Published | 2009 |
Keywords | Algorithms, DNA, Complementary, DNA, Fungal, Gene Expression Profiling, Oligonucleotide Array Sequence Analysis, Saccharomyces cerevisiae, Sequence Alignment, Sequence Analysis, DNA |
Abstract | BACKGROUND: 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. RESULTS: 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 S. cerevisiae. CONCLUSION: 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 S. cerevisiae that indicate full length cDNA sequencing can discover heterozygosity and measure quantitative allele-specific expression simultaneously. |
Alternate Journal | BMC Genomics |