Evidence map›Paper›PMID 26434581›Full record

ArticleScientific reports2015

mirPRo-a novel standalone program for differential expression and variation analysis of miRNAs.

Jieming Shi, Min Dong, Lei Li, Lin Liu, Agustin Luz-Madrigal, Panagiotis A Tsonis, Katia Del Rio-Tsonis, Chun Liang

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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  9. Hatching is modulated by microRNA-378a-3p derived from extracellular vesicles secreted by blastocysts.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  18. MicroRNAs Regulating Autophagy in Neurodegeneration.Advances in experimental medicine and biology · 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

8 authors.

Jieming ShiDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.
Min DongDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.
Lei LiDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.
Lin LiuDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.
Agustin Luz-MadrigalDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.
Panagiotis A TsonisDepartment of Biology, University of Dayton and Center for Tissue Regeneration and Engineering at the University of Dayton (TREND), Dayton, Ohio 45469, USA.
Katia Del Rio-TsonisDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.
Chun LiangDepartment of Biology, Miami University and Center for Visual Sciences at Miami University, Oxford, Ohio 45056, USA.

Funding

GENE REGULATION IN LENS REGENERATIONR01EY010540 · NEI · UNIVERSITY OF DAYTON · PI TSONIS, PANAGIOTIS A · 1995 to 2013
$3.3M
Retinal Pigmented Epithelium Reprogramming and Retina RegenerationR21EY023925 · NEI · MIAMI UNIVERSITY OXFORD · PI DEL RIO-TSONIS, KATIA · 2013 to 2014
$387k
NEI NIH HHS EY10540NEI NIH HHS R01 EY010540NEI NIH HHS R21 EY023925NEI NIH HHS R21EY023925-01
6 · The paper itself

Abstract

Being involved in many important biological processes, miRNAs can regulate gene expression by targeting mRNAs to facilitate their degradation or translational inhibition. Many miRNA sequencing studies reveal that miRNA variations such as isomiRs and "arm switching" are biologically relevant. However, existing standalone tools usually do not provide comprehensive, detailed information on miRNA variations. To deepen our understanding of miRNA variability, we developed a new standalone tool called "mirPRo" to quantify known miRNAs and predict novel miRNAs. Compared with the most widely used standalone program, miRDeep2, mirPRo offers several new functions including read cataloging based on genome annotation, optional seed region check, miRNA family expression quantification, isomiR identification and categorization, and "arm switching" detection. Our comparative data analyses using three datasets from mouse, human and chicken demonstrate that mirPRo is more accurate than miRDeep2 by avoiding over-counting of sequence reads and by implementing different approaches in adapter trimming, mapping and quantification. mirPRo is an open-source standalone program (https://sourceforge.net/projects/mirpro/).

Indexed as

Gene Expression ProfilingSoftwareAnimalsBase SequenceHumansMiceMicroRNAsSequence Analysis, RNATranscriptomeMicroRNAs

Identifiers

PMID26434581
PMCPMC4592965

What OpenQuestion holds

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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.