MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1474-760X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing ; volume:15 ; number:1 ; day:13 ; month:1 ; year:2014 ; pages:1-20 ; date:1.2014
Genome biology ; 15, Heft 1 (13.1.2014), 1-20, 1.2014

Creator: Mort, Matthew

Contributor: Sterne-Weiler, Timothy
Li, Biao
Ball, Edward V.
Cooper, David N.
Radivojac, Predrag
Sanford, Jeremy R.
Mooney, Sean D.
SpringerLink (Online service)

DOI: 10.1186/gb-2014-15-1-r19

URN: urn:nbn:de:1111-2016050211556

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:48 AM CEST

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Mort, Matthew
Sterne-Weiler, Timothy
Li, Biao
Ball, Edward V.
Cooper, David N.
Radivojac, Predrag
Sanford, Jeremy R.
Mooney, Sean D.
SpringerLink (Online service)

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MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing

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Other Objects (12)

Splice-disrupt genomic variants in prostate cancer

TREM2 splice isoforms generate soluble TREM2 species that disrupt long-term potentiation

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Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2transcripts

Exon identity crisis: disease-causing mutations that disrupt the splicing code

Cross-kingdom patterns of alternative splicing and splice recognition

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

SpliceTransformer predicts tissue-specific splicing linked to human diseases

SimSpliceEvol: alternative splicing-aware simulation of biological sequence evolution

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Systematic analysis of CNGA3 splice variants identifies different mechanisms of aberrant splicing

KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data

Splice-disrupt genomic variants in prostate cancer

TREM2 splice isoforms generate soluble TREM2 species that disrupt long-term potentiation

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2transcripts

Exon identity crisis: disease-causing mutations that disrupt the splicing code

Cross-kingdom patterns of alternative splicing and splice recognition

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

SpliceTransformer predicts tissue-specific splicing linked to human diseases

SimSpliceEvol: alternative splicing-aware simulation of biological sequence evolution

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KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data

Splice-disrupt genomic variants in prostate cancer

TREM2 splice isoforms generate soluble TREM2 species that disrupt long-term potentiation

SpliceAI-visual: a free online tool to improve SpliceAI splicing variant interpretation

Effect of BRCA2 sequence variants predicted to disrupt exonic splice enhancers on BRCA2transcripts

Exon identity crisis: disease-causing mutations that disrupt the splicing code

Cross-kingdom patterns of alternative splicing and splice recognition

Benchmarking splice variant prediction algorithms using massively parallel splicing assays

SpliceTransformer predicts tissue-specific splicing linked to human diseases

SimSpliceEvol: alternative splicing-aware simulation of biological sequence evolution

All reported non-canonical splice site variants in GLA cause aberrant splicing

Systematic analysis of CNGA3 splice variants identifies different mechanisms of aberrant splicing

KIS SPLICE: de-novo calling alternative splicing events from RNA-seq data

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