Evidence map›Paper›PMID 33079938›Full record

ArticlePLoS computational biology2020

seekCRIT: Detecting and characterizing differentially expressed circular RNAs using high-throughput sequencing data.

Mohamed Chaabane, Kalina Andreeva, Jae Yeon Hwang, Tae Lim Kook, Juw Won Park, Nigel G F Cooper

Abstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Circular RNA PTPN4 Contributes to Blood-Brain Barrier Disruption during Early Epileptogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

6 authors.

Mohamed ChaabaneDepartment of Computer Science and Engineering, University of Louisville, Louisville, Kentucky, United States of America.
Kalina AndreevaDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, Kentucky, United States of America.ORCID 0000-0002-5206-532X
Jae Yeon HwangDepartment of Computer Science and Engineering, University of Louisville, Louisville, Kentucky, United States of America.ORCID 0000-0002-7247-0146
Tae Lim KookDepartment of Computer Science and Engineering, University of Louisville, Louisville, Kentucky, United States of America.ORCID 0000-0003-2505-3443
Juw Won ParkDepartment of Computer Science and Engineering, University of Louisville, Louisville, Kentucky, United States of America.ORCID 0000-0002-4610-6893
Nigel G F CooperDepartment of Anatomical Sciences and Neurobiology, University of Louisville, Louisville, Kentucky, United States of America.ORCID 0000-0001-6598-5136

Funding

WKU Lead Faculty AwardP20GM103436 · NIGMS · UNIVERSITY OF LOUISVILLE · PI ERIC C ROUCHKA · 2012 to 2026
$60.1M
Detecting and characterizing circular RNAs using high-throughput sequencing dataR15GM126446 · NIGMS · UNIVERSITY OF LOUISVILLE · PI PARK, JUW WON · 2017 to 2017
$462k
NIGMS NIH HHS P20 GM103436NIGMS NIH HHS R15 GM126446
6 · The paper itself

Abstract

Over the past two decades, researchers have discovered a special form of alternative splicing that produces a circular form of RNA. Although these circular RNAs (circRNAs) have garnered considerable attention in the scientific community for their biogenesis and functions, the focus of current studies has been on the tissue-specific circRNAs that exist only in one tissue but not in other tissues or on the disease-specific circRNAs that exist in certain disease conditions, such as cancer, but not under normal conditions. This approach was conducted in the relative absence of methods that analyze a group of common circRNAs that exist in both conditions, but are more abundant in one condition relative to another (differentially expressed). Studies of differentially expressed circRNAs (DECs) between two conditions would serve as a significant first step in filling this void. Here, we introduce a novel computational tool, seekCRIT (seek for differentially expressed CircRNAs In Transcriptome), that identifies the DECs between two conditions from high-throughput sequencing data. Using rat retina RNA-seq data from ischemic and normal conditions, we show that over 74% of identifiable circRNAs are expressed in both conditions and over 40 circRNAs are differentially expressed between two conditions. We also obtain a high qPCR validation rate of 90% for DECs with a FDR of < 5%. Our results demonstrate that seekCRIT is a novel and efficient approach to detect DECs using rRNA depleted RNA-seq data. seekCRIT is freely downloadable at https://github.com/UofLBioinformatics/seekCRIT. The source code is licensed under the MIT License. seekCRIT is developed and tested on Linux CentOS-7.

Indexed as

RNA, CircularAnimalsComputational BiologyDatabases, GeneticGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansRatsSequence Analysis, RNASoftwareTranscriptomeRNA, Circular

Identifiers

PMID33079938
PMCPMC7598922

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.