
doi: 10.1038/nmeth.1503
pmid: 20835245
In alternative expression analysis by sequencing (ALEXA-seq), we developed a method to analyze massively parallel RNA sequence data to catalog transcripts and assess differential and alternative expression of known and predicted mRNA isoforms in cells and tissues. As proof of principle, we used the approach to compare fluorouracil-resistant and -nonresistant human colorectal cancer cell lines. We assessed the sensitivity and specificity of the approach by comparison to exon tiling and splicing microarrays and validated the results with reverse transcription-PCR, quantitative PCR and Sanger sequencing. We observed global disruption of splicing in fluorouracil-resistant cells characterized by expression of new mRNA isoforms resulting from exon skipping, alternative splice site usage and intron retention. Alternative expression annotation databases, source code, a data viewer and other resources to facilitate analysis are available at http://www.alexaplatform.org/alexa_seq/.
Expressed Sequence Tags, Antimetabolites, Antineoplastic, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, RNA, Gene Expression Profiling, Gene Expression, Alternative Splicing, Drug Resistance, Neoplasm, Cell Line, Tumor, Databases, Genetic, Humans, Protein Isoforms, Fluorouracil, RNA, Messenger, Colorectal Neoplasms, Sequence Alignment, Oligonucleotide Array Sequence Analysis
Expressed Sequence Tags, Antimetabolites, Antineoplastic, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, RNA, Gene Expression Profiling, Gene Expression, Alternative Splicing, Drug Resistance, Neoplasm, Cell Line, Tumor, Databases, Genetic, Humans, Protein Isoforms, Fluorouracil, RNA, Messenger, Colorectal Neoplasms, Sequence Alignment, Oligonucleotide Array Sequence Analysis
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