Evidence map›Paper›PMID 17456239›Full record

ArticleGenome biology2007

Discovery of tissue-specific exons using comprehensive human exon microarrays.

Tyson A Clark, Anthony C Schweitzer, Tina X Chen, Michelle K Staples, Gang Lu, Hui Wang, Alan Williams, John E Blume

Abstract read
In one paragraph

Article in Genome biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 185 papers.

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0cells of the map it votes in
185citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

185 citing papers in PubMed.

  1. Trial
  2. Microarrays and the Dawn of Omics Data Analysis.Advances in experimental medicine and biology · 2026
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  3. An Overview of Circular RNAs.Advances in experimental medicine and biology · 2025
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  5. Revealing the History and Mystery of RNA-Seq.Current issues in molecular biology · 2023
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  10. Review
  11. Processing and Analysis of RNA-seq Data from Public Resources.Methods in molecular biology (Clifton, N.J.) · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

125 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Tyson A ClarkAffymetrix, Inc, Santa Clara, CA 95051, USA. tyson_clark@affymetrix.com
Anthony C Schweitzer
Tina X Chen
Michelle K Staples
Gang Lu
Hui Wang
Alan Williams
John E Blume

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigher eukaryotes express a diverse population of messenger RNAs generated by alternative splicing. Large-scale methods for monitoring gene expression must adapt in order to accurately detect the transcript variation generated by this splicing.

resultsWe have designed a high-density oligonucleotide microarray with probesets for more than one million annotated and predicted exons in the human genome. Using these arrays and a simple algorithm that normalizes exon signal to signal from the gene as a whole, we have identified tissue-specific exons from a panel of 16 different normal adult tissues. RT-PCR validation confirms approximately 86% of the predicted tissue-enriched probesets. Pair-wise comparisons between the tissues suggest that as many as 73% of detected genes are differentially alternatively spliced. We also demonstrate how an inclusive exon microarray can be used to discover novel alternative splicing events. As examples, 17 new tissue-specific exons from 11 genes were validated by RT-PCR and sequencing.

conclusionIn conjunction with a conceptually simple algorithm, comprehensive exon microarrays can detect tissue-specific alternative splicing events. Our data suggest significant expression outside of known exons and well annotated genes and a high frequency of alternative splicing events. In addition, we identified and validated a number of novel exons with tissue-specific splicing patterns. The tissue map data will likely serve as a valuable source of information on the regulation of alternative splicing.

Indexed as

Alternative SplicingExonsAlgorithmsBrainGene Expression ProfilingHumansOligonucleotide Array Sequence AnalysisRNA, MessengerRNA, Messenger

Identifiers

PMID17456239
PMCPMC1896007

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.