Evidence map›Paper›PMID 29931155›Full record

ReviewBriefings in bioinformatics2019

Exploring the functional impact of alternative splicing on human protein isoforms using available annotation sources.

Dinanath Sulakhe, Mark D'Souza, Sheng Wang, Sandhya Balasubramanian, Prashanth Athri, Bingqing Xie, Stefan Canzar, Gady Agam, T Conrad Gilliam, Natalia Maltsev

Open access · bronzeAbstract readReview
In one paragraph

Review in Briefings in bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

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  11. SpliceProt 2.0: A Sequence Repository of Human, Mouse, and Rat Proteoforms.International journal of molecular sciences · 2024
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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

10 authors at 4 institutions in 3 countries.

Dinanath SulakheDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
Mark D'SouzaDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
Sheng WangDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
Sandhya BalasubramanianDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
Prashanth AthriDepartment of Computer Science and Engineering, Amrita School of Engineering, Bengaluru, Amrita Vishwa Vidyapeetham, Kasavanahalli, Carmelaram P.O., Bengaluru, Karnataka, India.
Bingqing XieDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
Stefan CanzarToyota Technological Institute at Chicago, 6045 S. Kenwood Avenue, Chicago, IL, USA.
Gady AgamDepartment of Computer Science, Illinois Institute of Technology, Chicago, IL, USA.
T Conrad GilliamDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
Natalia MaltsevDepartment of Human Genetics, University of Chicago, 920 E. 58th Street, Chicago, IL, USA.
University of Chicago · USIllinois Institute of Technology · USToyota Technological Institute at Chicago · USAmrita Vishwa Vidyapeetham · IN

Funding

Center for Genomic and Phenomic Studies in AutismU24MH081810 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI LAJONCHERE, CLARA M · 2007 to 2011
$8.3M
NIMH NIH HHS U24 MH081810
6 · The paper itself

Abstract

In recent years, the emphasis of scientific inquiry has shifted from whole-genome analyses to an understanding of cellular responses specific to tissue, developmental stage or environmental conditions. One of the central mechanisms underlying the diversity and adaptability of the contextual responses is alternative splicing (AS). It enables a single gene to encode multiple isoforms with distinct biological functions. However, to date, the functions of the vast majority of differentially spliced protein isoforms are not known. Integration of genomic, proteomic, functional, phenotypic and contextual information is essential for supporting isoform-based modeling and analysis. Such integrative proteogenomics approaches promise to provide insights into the functions of the alternatively spliced protein isoforms and provide high-confidence hypotheses to be validated experimentally. This manuscript provides a survey of the public databases supporting isoform-based biology. It also presents an overview of the potential global impact of AS on the human canonical gene functions, molecular interactions and cellular pathways.

Indexed as

Alternative SplicingComputational BiologyDatabases, ProteinHumansProtein IsoformsProtein Isoformsalternative splicingcontext-specificinteractionisoformpathwayprotein function

Identifiers

PMID29931155
PMCPMC6917224
OpenAlexW2809400819

What OpenQuestion holds

Textmetadata
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.