SimSpliceEvol: alternative splicing-aware simulation of biological sequence evolution

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2105

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: SimSpliceEvol: alternative splicing-aware simulation of biological sequence evolution ; volume:20 ; number:20 ; day:17 ; month:12 ; year:2019 ; pages:1-13 ; date:12.2019
BMC bioinformatics ; 20, Heft 20 (17.12.2019), 1-13, 12.2019

Creator: Kuitche, Esaie
Jammali, Safa
Ouangraoua, Aïda

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12859-019-3207-5

URN: urn:nbn:de:101:1-2020040523170947929878

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:45 AM CEST

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Kuitche, Esaie
Jammali, Safa
Ouangraoua, Aïda
SpringerLink (Online service)

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SimSpliceEvol2: alternative splicing-aware simulation of biological sequence evolution and transcript phylogenies

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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

Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework

Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive

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

Modulation of 5' splice site selection using tailed oligonucleotides carrying splicing signals

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

SimSpliceEvol2: alternative splicing-aware simulation of biological sequence evolution and transcript phylogenies

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

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

Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework

Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive

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

Modulation of 5' splice site selection using tailed oligonucleotides carrying splicing signals

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

SimSpliceEvol2: alternative splicing-aware simulation of biological sequence evolution and transcript phylogenies

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

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

Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework

Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive

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

Modulation of 5' splice site selection using tailed oligonucleotides carrying splicing signals

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

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SimSpliceEvol: alternative splicing-aware simulation of biological sequence evolution

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Other Objects (12)

SimSpliceEvol2: alternative splicing-aware simulation of biological sequence evolution and transcript phylogenies

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

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

Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework

Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive

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

Modulation of 5' splice site selection using tailed oligonucleotides carrying splicing signals

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

SimSpliceEvol2: alternative splicing-aware simulation of biological sequence evolution and transcript phylogenies

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

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

Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework

Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive

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

Modulation of 5' splice site selection using tailed oligonucleotides carrying splicing signals

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

SimSpliceEvol2: alternative splicing-aware simulation of biological sequence evolution and transcript phylogenies

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

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

Splice_sim: a nucleotide conversion-enabled RNA-seq simulation and evaluation framework

Human splicing diversity and the extent of unannotated splice junctions across human RNA-seq samples on the Sequence Read Archive

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

Modulation of 5' splice site selection using tailed oligonucleotides carrying splicing signals

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

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