Evidence map›Paper›PMID 32534132›Full record

ArticleMethods (San Diego, Calif.)2021

A network-based computational framework to predict and differentiate functions for gene isoforms using exon-level expression data.

Dingjie Wang, Xiufen Zou, Kin Fai Au

Open access · greenAbstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 46% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
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

3 authors at 2 institutions in 2 countries.

Dingjie WangDepartment of Biomedical Informatics, The Ohio State University, OH 43210, USA; School of Mathematics and Statistics, Wuhan University, Wuhan 430072, China; Computational Science Hubei Key Laboratory, Wuhan University, Wuhan 430072, China.
Xiufen ZouSchool of Mathematics and Statistics, Wuhan University, Wuhan 430072, China; Computational Science Hubei Key Laboratory, Wuhan University, Wuhan 430072, China. Electronic address: xfzou@whu.edu.cn.
Kin Fai AuDepartment of Biomedical Informatics, The Ohio State University, OH 43210, USA. Electronic address: kinfai.au@osumc.edu.
The Ohio State University · USWuhan University · CN

Funding

Bioinformatics platform for Hybrid-Seq transcriptome data analysisR01HG008759 · NHGRI · UNIVERSITY OF IOWA · PI AU, KIN FAI · 2016 to 2020
$1.9M
NHGRI NIH HHS R01 HG008759
6 · The paper itself

Abstract

motivationAlternative splicing makes significant contributions to functional diversity of transcripts and proteins. Many alternatively spliced gene isoforms have been shown to perform specific biological functions under different contexts. In addition to gene-level expression, the advances of high-throughput sequencing offer a chance to estimate isoform-specific exon expression with a high resolution, which is informative for studying splice variants with network analysis.

resultsIn this study, we propose a novel network-based analysis framework to predict isoform-specific functions from exon-level RNA-Seq data. In particular, based on exon-level expression data, we firstly propose a unified framework, referred to as Iso-Net, to integrate two new mathematical methods (named MINet and RVNet) that infer co-expression networks at different data scenarios. We demonstrate the superior prediction accuracy of Iso-Net over the existing methods for most simulation data, especially in two extreme cases: sample size is very small and exon numbers of two isoforms are quite different. Furthermore, by defining relevant quantitative measures (e.g., Jaccard correlation coefficient) and combining differential co-expression network analysis and GO functional enrichment analysis, a co-expression network analysis framework is developed to predict functions of isoforms and further, to discover their distinct functions within the same gene. We apply Iso-Net to study gene isoforms for several important transcription factors in human myeloid differentiation with the exon-level RNA-Seq data from three different cell lines. AVAILABILITY AND IMPLEMENTATION: Iso-Net is open source and freely available from https://github.com/Dingjie-Wang/Iso-Net.

Indexed as

Alternative SplicingExonsNeural Networks, ComputerProtein IsoformsSoftwareComputational BiologyGene Expression RegulationHigh-Throughput Nucleotide SequencingHumansSequence Analysis, RNAProtein IsoformsAlternative splicingCo-expression networksExon-level RNA-SeqGene isoformsMatrix Correlation

Identifiers

PMID32534132
PMCPMC9628273
OpenAlexW3034188525

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.