Evidence map›Paper›PMID 32228441›Full record

ArticleBMC genomics2020

A large-scale comparative study of isoform expressions measured on four platforms.

Wei Zhang, Raphael Petegrosso, Jae-Woong Chang, Jiao Sun, Jeongsik Yong, Jeremy Chien, Rui Kuang

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Cross-assay RNA modeling reveals cancer biomarkers.bioRxiv : the preprint server for biology · 2026
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  13. Frontiers in immunology · 2021
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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

7 authors at 3 institutions in 1 country.

Wei ZhangDepartment of Computer Science, University of Central Florida, 4000 Central Florida Blvd, Orlando, 32816, FL, USA.
Raphael PetegrossoDepartment of Computer Science and Engineering, University of Minnesota Twin Cities, 200 Union Street SE, Minneapolis, 55455, MN, USA.
Jae-Woong ChangDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota Twin Cities, 200 Union Street SE, Minneapolis, 55455, MN, USA.
Jiao SunDepartment of Computer Science, University of Central Florida, 4000 Central Florida Blvd, Orlando, 32816, FL, USA.
Jeongsik YongDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota Twin Cities, 200 Union Street SE, Minneapolis, 55455, MN, USA.
Jeremy ChienDepartment of Biochemistry and Molecular Medicine, University of California, Davis, 2700 Stockton Blvd., Sacramento, 95817, CA, USA.
Rui KuangDepartment of Computer Science and Engineering, University of Minnesota Twin Cities, 200 Union Street SE, Minneapolis, 55455, MN, USA. kuang@umn.edu.ORCID http://orcid.org/0000-0003-3605-9373
University of Minnesota · USUniversity of Central Florida · USUniversity of California, Davis · US

Funding

The Role of Truncated mRNAs in CancerR01GM113952 · NIGMS · UNIVERSITY OF MINNESOTA · PI YONG, JEONGSIK · 2015 to 2023
$3.0M
NIGMS NIH HHS R01 GM113952NIGMS NIH HHS R01GM113952
6 · The paper itself

Abstract

backgroundMost eukaryotic genes produce different transcripts of multiple isoforms by inclusion or exclusion of particular exons. The isoforms of a gene often play diverse functional roles, and thus it is necessary to accurately measure isoform expressions as well as gene expressions. While previous studies have demonstrated the strong agreement between mRNA sequencing (RNA-seq) and array-based gene and/or isoform quantification platforms (Microarray gene expression and Exon-array), the more recently developed NanoString platform has not been systematically evaluated and compared, especially in large-scale studies across different cancer domains.

resultsIn this paper, we present a large-scale comparative study among RNA-seq, NanoString, array-based, and RT-qPCR platforms using 46 cancer cell lines across different cancer types. The goal is to understand and evaluate the calibers of the platforms for measuring gene and isoform expressions in cancer studies. We first performed NanoString experiments on 59 cancer cell lines with 404 custom-designed probes for measuring the expressions of 478 isoforms in 155 genes, and additional RT-qPCR experiments for a subset of the measured isoforms in 13 cell lines. We then combined the data with the matched RNA-seq, Exon-array, and Microarray data of 46 of the 59 cell lines for the comparative analysis.

conclusionIn the comparisons of the platforms for measuring the expressions at both isoform and gene levels, we found that (1) the agreement on isoform expressions is lower than the agreement on gene expressions across the four platforms; (2) NanoString and Exon-array are not consistent on isoform quantification even though both techniques are based on hybridization reactions; (3) RT-qPCR experiments are more consistent with RNA-seq and Exon-array than NanoString in isoform quantification; (4) different RNA-seq isoform quantification methods show varying estimation results, and among the methods, Net-RSTQ and eXpress are more consistent across the platforms; and (5) RNA-seq has the best overall consistency with the other platforms on gene expression quantification.

Indexed as

AlgorithmsExonsGene Expression ProfilingHumansOligonucleotide Array Sequence AnalysisProtein IsoformsSequence Analysis, RNASoftwareProtein IsoformsCross-platform comparisonExon-arrayIsoform-level expressionMicroarray gene expressionNanoStringRNA-seq

Identifiers

PMID32228441
PMCPMC7106849
OpenAlexW3013053182

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.