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      A gene atlas of the mouse and human protein-encoding transcriptomes.

      Proceedings of the National Academy of Sciences of the United States of America
      Animals, Female, Genomic Imprinting, Humans, Male, Mice, RNA, Messenger, genetics, Transcription, Genetic

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          Abstract

          The tissue-specific pattern of mRNA expression can indicate important clues about gene function. High-density oligonucleotide arrays offer the opportunity to examine patterns of gene expression on a genome scale. Toward this end, we have designed custom arrays that interrogate the expression of the vast majority of protein-encoding human and mouse genes and have used them to profile a panel of 79 human and 61 mouse tissues. The resulting data set provides the expression patterns for thousands of predicted genes, as well as known and poorly characterized genes, from mice and humans. We have explored this data set for global trends in gene expression, evaluated commonly used lines of evidence in gene prediction methodologies, and investigated patterns indicative of chromosomal organization of transcription. We describe hundreds of regions of correlated transcription and show that some are subject to both tissue and parental allele-specific expression, suggesting a link between spatial expression and imprinting.

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          Most cited references24

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          BLAT---The BLAST-Like Alignment Tool

          W. J. Kent (2002)
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            Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.

            Only a small proportion of the mouse genome is transcribed into mature messenger RNA transcripts. There is an international collaborative effort to identify all full-length mRNA transcripts from the mouse, and to ensure that each is represented in a physical collection of clones. Here we report the manual annotation of 60,770 full-length mouse complementary DNA sequences. These are clustered into 33,409 'transcriptional units', contributing 90.1% of a newly established mouse transcriptome database. Of these transcriptional units, 4,258 are new protein-coding and 11,665 are new non-coding messages, indicating that non-coding RNA is a major component of the transcriptome. 41% of all transcriptional units showed evidence of alternative splicing. In protein-coding transcripts, 79% of splice variations altered the protein product. Whole-transcriptome analyses resulted in the identification of 2,431 sense-antisense pairs. The present work, completely supported by physical clones, provides the most comprehensive survey of a mammalian transcriptome so far, and is a valuable resource for functional genomics.
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              Exploring the Metabolic and Genetic Control of Gene Expression on a Genomic Scale

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                Author and article information

                Journal
                15075390
                395923
                10.1073/pnas.0400782101

                Chemistry
                Animals,Female,Genomic Imprinting,Humans,Male,Mice,RNA, Messenger,genetics,Transcription, Genetic
                Chemistry
                Animals, Female, Genomic Imprinting, Humans, Male, Mice, RNA, Messenger, genetics, Transcription, Genetic

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