Evidence map›Paper›PMID 29567976›Full record

ArticleScientific reports2018

SpliceDetector: a software for detection of alternative splicing events in human and model organisms directly from transcript IDs.

Mandana Baharlou Houreh, Payam Ghorbani Kalkhajeh, Ali Niazi, Faezeh Ebrahimi, Esmaeil Ebrahimie

Abstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Understanding small ORF diversity through a comprehensive transcription feature classification.DNA research : an international journal for rapid publication of reports on genes and genomes · 2021
    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

5 authors.

Mandana Baharlou HourehInstitute of Biotechnology, Shiraz University, Shiraz, Iran.
Payam Ghorbani KalkhajehScience and Research Branch, Islamic Azad university, Hamedan, Iran.
Ali NiaziInstitute of Biotechnology, Shiraz University, Shiraz, Iran.
Faezeh EbrahimiDepartment of Biology, University of Qom, Qom, Iran.
Esmaeil EbrahimieInstitute of Biotechnology, Shiraz University, Shiraz, Iran. esmaeil.ebrahimie@adelaide.edu.au.ORCID 0000-0003-1699-3476

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In eukaryotes, different combinations of exons lead to multiple transcripts with various functions in protein level, in a process called alternative splicing (AS). Unfolding the complexity of functional genomics through genome-wide profiling of AS and determining the altered ultimate products provide new insights for better understanding of many biological processes, disease progress as well as drug development programs to target harmful splicing variants. The current available tools of alternative splicing work with raw data and include heavy computation. In particular, there is a shortcoming in tools to discover AS events directly from transcripts. Here, we developed a Windows-based user-friendly tool for identifying AS events from transcripts without the need to any advanced computer skill or database download. Meanwhile, due to online working mode, our application employs the updated SpliceGraphs without the need to any resource updating. First, SpliceGraph forms based on the frequency of active splice sites in pre-mRNA. Then, the presented approach compares query transcript exons to SpliceGraph exons. The tool provides the possibility of statistical analysis of AS events as well as AS visualization compared to SpliceGraph. The developed application works for transcript sets in human and model organisms.

Indexed as

SoftwareAlternative SplicingDatabase Management SystemsDatabases, FactualExonsGenomicsHumansIntronsModels, AnimalRNA Splice SitesRNA SplicingUser-Computer InterfaceRNA Splice Sites

Identifiers

PMID29567976
PMCPMC5864913

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.