Evidence map›Paper›PMID 34266387›Full record

ArticleBMC bioinformatics2021

SPLICE-q: a Python tool for genome-wide quantification of splicing efficiency.

Verônica R de Melo Costa, Julianus Pfeuffer, Annita Louloupi, Ulf A V Ørom, Rosario M Piro

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  12. Global impact of aberrant splicing on human gene expression levels.bioRxiv : the preprint server for biology · 2023
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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

5 authors at 5 institutions in 3 countries.

Verônica R de Melo CostaInstitute of Computer Science and Institute of Bioinformatics, Freie Universität Berlin, Berlin, Germany. veronica.melocosta@gmail.com.
Julianus PfeufferInstitute of Computer Science and Institute of Bioinformatics, Freie Universität Berlin, Berlin, Germany.
Annita LouloupiMax Delbrück Center for Molecular Medicine, Berlin Institute for Medical Systems Biology, Berlin, Germany.
Ulf A V ØromDepartment of Molecular Biology and Genetics, Aarhus University, Aarhus, Denmark.
Rosario M PiroDipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, Milan, Italy. rosariomichael.piro@polimi.it.ORCID http://orcid.org/0000-0002-3066-7397
Aarhus University · DKFreie Universität Berlin · DEMax Delbrück Center · DEMax Planck Institute for Molecular Genetics · DEPolitecnico di Milano · IT

Funding

Bundesministerium für Bildung und Forschung FKZ 031A535ACoordenação de Aperfeiçoamento de Pessoal de Nível Superior BEX 99999.002121/2015-08
6 · The paper itself

Abstract

backgroundIntrons are generally removed from primary transcripts to form mature RNA molecules in a post-transcriptional process called splicing. An efficient splicing of primary transcripts is an essential step in gene expression and its misregulation is related to numerous human diseases. Thus, to better understand the dynamics of this process and the perturbations that might be caused by aberrant transcript processing it is important to quantify splicing efficiency.

resultsHere, we introduce SPLICE-q, a fast and user-friendly Python tool for genome-wide SPLICing Efficiency quantification. It supports studies focusing on the implications of splicing efficiency in transcript processing dynamics. SPLICE-q uses aligned reads from strand-specific RNA-seq to quantify splicing efficiency for each intron individually and allows the user to select different levels of restrictiveness concerning the introns' overlap with other genomic elements such as exons of other genes. We applied SPLICE-q to globally assess the dynamics of intron excision in yeast and human nascent RNA-seq. We also show its application using total RNA-seq from a patient-matched prostate cancer sample.

conclusionsOur analyses illustrate that SPLICE-q is suitable to detect a progressive increase of splicing efficiency throughout a time course of nascent RNA-seq and it might be useful when it comes to understanding cancer progression beyond mere gene expression levels. SPLICE-q is available at: https://github.com/vrmelo/SPLICE-q.

Indexed as

Alternative SplicingRNA Splice SitesGenomeHumansIntronsRNA SplicingRNA Splice SitesCo-transcriptional splicingRNA-seqSplicing dynamicsSplicing efficiency

Identifiers

PMID34266387
PMCPMC8281633
OpenAlexW3181822107

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.