Evidence map›Paper›PMID 32966552›Full record

ArticleBioinformatics (Oxford, England)2021

IsoResolve: predicting splice isoform functions by integrating gene and isoform-level features with domain adaptation.

Hong-Dong Li, Changhuo Yang, Zhimin Zhang, Mengyun Yang, Fang-Xiang Wu, Gilbert S Omenn, Jianxin Wang

Abstract read
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Article in Bioinformatics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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8citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. ProteoformDB: an integrative database for functional roles of proteoforms.Database : the journal of biological databases and curation · 2026
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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hong-Dong LiHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering.ORCID 0000-0003-3438-739X
Changhuo YangHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering.
Zhimin ZhangCollege of Chemistry and Chemical Engineering, Central South University, Changsha, Hunan 410083, China.
Mengyun YangHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering.
Fang-Xiang WuDivision of Biomedical Engineering, University of Saskatchewan, Saskatoon, SK S7N5A9, Canada.ORCID 0000-0002-4593-9332
Gilbert S OmennInstitute for Systems Biology, Seattle, WA 98101, USA.
Jianxin WangHunan Provincial Key Lab on Bioinformatics, School of Computer Science and Engineering.ORCID 0000-0003-1516-0480

Funding

Strategic Vision & Impact on Environmental HealthP30ES017885 · NIEHS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Dana Dolinoy · 2011 to 2026
$21.3M
University of Michigan Proteogenomics Data Analysis CenterU24CA210967 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, DHANASEKARAN, SARAVANA M · 2016 to 2020
$4.1M
NCI NIH HHS U24 CA210967NIEHS NIH HHS P30 ES017885
6 · The paper itself

Abstract

motivationHigh resolution annotation of gene functions is a central goal in functional genomics. A single gene may produce multiple isoforms with different functions through alternative splicing. Conventional approaches, however, consider a gene as a single entity without differentiating these functionally different isoforms. Towards understanding gene functions at higher resolution, recent efforts have focused on predicting the functions of isoforms. However, the performance of existing methods is far from satisfactory mainly because of the lack of isoform-level functional annotation.

resultsWe present IsoResolve, a novel approach for isoform function prediction, which leverages the information from gene function prediction models with domain adaptation (DA). IsoResolve treats gene-level and isoform-level features as source and target domains, respectively. It uses DA to project the two domains into a latent variable space in such a way that the latent variables from the two domains have similar distribution, which enables the gene domain information to be leveraged for isoform function prediction. We systematically evaluated the performance of IsoResolve in predicting functions. Compared with five state-of-the-art methods, IsoResolve achieved significantly better performance. IsoResolve was further validated by case studies of genes with isoform-level functional annotation. AVAILABILITY AND IMPLEMENTATION: IsoResolve is freely available at https://github.com/genemine/IsoResolve. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Adaptation, PhysiologicalAlternative SplicingComputational BiologyMutationProtein IsoformsProtein Isoforms

Identifiers

PMID32966552
PMCPMC8088322

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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.