MAJIQlopedia: an encyclopedia of RNA splicing variations in human tissues and cancer.


Journal

Nucleic acids research
ISSN: 1362-4962
Titre abrégé: Nucleic Acids Res
Pays: England
ID NLM: 0411011

Informations de publication

Date de publication:
11 Nov 2023
Historique:
accepted: 02 11 2023
revised: 11 10 2023
received: 15 08 2023
medline: 13 11 2023
pubmed: 13 11 2023
entrez: 12 11 2023
Statut: aheadofprint

Résumé

Quantification of RNA splicing variations based on RNA-Sequencing can reveal tissue- and disease-specific splicing patterns. To study such splicing variations, we introduce MAJIQlopedia, an encyclopedia of splicing variations that encompasses 86 human tissues and 41 cancer datasets. MAJIQlopedia reports annotated and unannotated splicing events for a total of 486 175 alternative splice junctions in normal tissues and 338 317 alternative splice junctions in cancer. This database, available at https://majiq.biociphers.org/majiqlopedia/, includes a user-friendly interface that provides graphical representations of junction usage quantification for each junction across all tissue or cancer types. To demonstrate case usage of MAJIQlopedia, we review splicing variations in genes WT1, MAPT and BIN1, which all have known tissue or cancer-specific splicing variations. We also use MAJIQlopedia to highlight novel splicing variations in FDX1 and MEGF9 in normal tissues, and we uncover a novel exon inclusion event in RPS6KA6 that only occurs in two cancer types. Users can download the database, request the addition of data to the webtool, or install a MAJIQlopedia server to integrate proprietary data. MAJIQlopedia can serve as a reference database for researchers seeking to understand what splicing variations exist in genes of interest, and those looking to understand tissue- or cancer-specific splice isoform usage.

Identifiants

pubmed: 37953365
pii: 7416386
doi: 10.1093/nar/gkad1043
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NCI NIH HHS
ID : U01 CA232563
Pays : United States
Organisme : NIH HHS
ID : CA232563
Pays : United States

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research.

Auteurs

Mathieu Quesnel-Vallières (M)

Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA 19104, USA.

San Jewell (S)

Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.

Kristen W Lynch (KW)

Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA 19104, USA.

Andrei Thomas-Tikhonenko (A)

Division of Cancer Pathobiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Oncology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Pathology & Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA.

Yoseph Barash (Y)

Department of Genetics, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Computer and Information Science, University of Pennsylvania, Philadelphia, PA, USA.

Classifications MeSH