Evidence map›Paper›PMID 39120880›Full record

ArticleBioinformatics (Oxford, England)2024

TransTEx: novel tissue-specificity scoring method for grouping human transcriptome into different expression groups.

Pallavi Surana, Pratik Dutta, Ramana V Davuluri

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. TSProm: Deciphering the Genomic Context of Tissue Specificity.bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Pallavi SuranaDepartment of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11794, USA.ORCID 0009-0004-4241-9181
Pratik DuttaDepartment of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11794, USA.
Ramana V DavuluriDepartment of Biomedical Informatics, Stony Brook University, Stony Brook, NY 11794, USA.ORCID 0000-0002-7053-1064

Funding

Developing Novel Deep-Learning Based Methods for Deciphering Non-Coding Gene Regulatory CodeR01LM013722 · NLM · STATE UNIVERSITY NEW YORK STONY BROOK · PI RAMANA V DAVULURI · 2021 to 2026
$2.0M
National Library of Medicine/National Institutes of Health R01LM013722NLM NIH HHS R01 LM013722
6 · The paper itself

Abstract

motivationAlthough human tissues carry out common molecular processes, gene expression patterns can distinguish different tissues. Traditional informatics methods, primarily at the gene level, overlook the complexity of alternative transcript variants and protein isoforms produced by most genes, changes in which are linked to disease prognosis and drug resistance.

resultsWe developed TransTEx (Transcript-level Tissue Expression), a novel tissue-specificity scoring method, for grouping transcripts into four expression groups. TransTEx applies sequential cut-offs to tissue-wise transcript probability estimates, subsampling-based P-values and fold-change estimates. Application of TransTEx on GTEx mRNA-seq data divided 199 166 human transcripts into different groups as 17 999 tissue-specific (TSp), 7436 tissue-enhanced, 36 783 widely expressed (Wide), 79 191 lowly expressed (Low), and 57 757 no expression (Null) transcripts. Testis has the most (13 466) TSp isoforms followed by liver (890), brain (701), pituitary (435), and muscle (420). We found that the tissue specificity of alternative transcripts of a gene is predominantly influenced by alternate promoter usage. By overlapping brain-specific transcripts with the cell-type gene-markers in scBrainMap database, we found that 63% of the brain-specific transcripts were enriched in nonneuronal cell types, predominantly astrocytes followed by endothelial cells and oligodendrocytes. In addition, we found 61 brain cell-type marker genes encoding a total of 176 alternative transcripts as brain-specific and 22 alternative transcripts as testis-specific, highlighting the complex TSp and cell-type specific gene regulation and expression at isoform-level. TransTEx can be adopted to the analysis of bulk RNA-seq or scRNA-seq datasets to find tissue- and/or cell-type specific isoform-level gene markers. AVAILABILITY AND IMPLEMENTATION: TransTEx database: https://bmi.cewit.stonybrook.edu/transtexdb/ and the R package is available via GitHub: https://github.com/pallavisurana1/TransTEx.

Indexed as

Organ SpecificityTranscriptomeGene Expression ProfilingHumansSoftware

Identifiers

PMID39120880
PMCPMC11319638

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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.