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

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          Abstract

          Abstract

          SpliceAI is an open-source deep learning splicing prediction algorithm that has demonstrated in the past few years its high ability to predict splicing defects caused by DNA variations. However, its outputs present several drawbacks: (1) although the numerical values are very convenient for batch filtering, their precise interpretation can be difficult, (2) the outputs are delta scores which can sometimes mask a severe consequence, and (3) complex delins are most often not handled. We present here SpliceAI-visual, a free online tool based on the SpliceAI algorithm, and show how it complements the traditional SpliceAI analysis. First, SpliceAI-visual manipulates raw scores and not delta scores, as the latter can be misleading in certain circumstances. Second, the outcome of SpliceAI-visual is user-friendly thanks to the graphical presentation. Third, SpliceAI-visual is currently one of the only SpliceAI-derived implementations able to annotate complex variants (e.g., complex delins). We report here the benefits of using SpliceAI-visual and demonstrate its relevance in the assessment/modulation of the PVS1 classification criteria. We also show how SpliceAI-visual can elucidate several complex splicing defects taken from the literature but also from unpublished cases. SpliceAI-visual is available as a Google Colab notebook and has also been fully integrated in a free online variant interpretation tool, MobiDetails ( https://mobidetails.iurc.montp.inserm.fr/MD).

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          The online version contains supplementary material available at 10.1186/s40246-023-00451-1.

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          Most cited references38

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          A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.

          We describe a new computer program, SnpEff, for rapidly categorizing the effects of variants in genome sequences. Once a genome is sequenced, SnpEff annotates variants based on their genomic locations and predicts coding effects. Annotated genomic locations include intronic, untranslated region, upstream, downstream, splice site, or intergenic regions. Coding effects such as synonymous or non-synonymous amino acid replacement, start codon gains or losses, stop codon gains or losses, or frame shifts can be predicted. Here the use of SnpEff is illustrated by annotating ~356,660 candidate SNPs in ~117 Mb unique sequences, representing a substitution rate of ~1/305 nucleotides, between the Drosophila melanogaster w(1118); iso-2; iso-3 strain and the reference y(1); cn(1) bw(1) sp(1) strain. We show that ~15,842 SNPs are synonymous and ~4,467 SNPs are non-synonymous (N/S ~0.28). The remaining SNPs are in other categories, such as stop codon gains (38 SNPs), stop codon losses (8 SNPs), and start codon gains (297 SNPs) in the 5'UTR. We found, as expected, that the SNP frequency is proportional to the recombination frequency (i.e., highest in the middle of chromosome arms). We also found that start-gain or stop-lost SNPs in Drosophila melanogaster often result in additions of N-terminal or C-terminal amino acids that are conserved in other Drosophila species. It appears that the 5' and 3' UTRs are reservoirs for genetic variations that changes the termini of proteins during evolution of the Drosophila genus. As genome sequencing is becoming inexpensive and routine, SnpEff enables rapid analyses of whole-genome sequencing data to be performed by an individual laboratory.
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            The Ensembl Variant Effect Predictor

            The Ensembl Variant Effect Predictor is a powerful toolset for the analysis, annotation, and prioritization of genomic variants in coding and non-coding regions. It provides access to an extensive collection of genomic annotation, with a variety of interfaces to suit different requirements, and simple options for configuring and extending analysis. It is open source, free to use, and supports full reproducibility of results. The Ensembl Variant Effect Predictor can simplify and accelerate variant interpretation in a wide range of study designs.
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              The Human Genome Browser at UCSC

              As vertebrate genome sequences near completion and research refocuses to their analysis, the issue of effective genome annotation display becomes critical. A mature web tool for rapid and reliable display of any requested portion of the genome at any scale, together with several dozen aligned annotation tracks, is provided at http://genome.ucsc.edu. This browser displays assembly contigs and gaps, mRNA and expressed sequence tag alignments, multiple gene predictions, cross-species homologies, single nucleotide polymorphisms, sequence-tagged sites, radiation hybrid data, transposon repeats, and more as a stack of coregistered tracks. Text and sequence-based searches provide quick and precise access to any region of specific interest. Secondary links from individual features lead to sequence details and supplementary off-site databases. One-half of the annotation tracks are computed at the University of California, Santa Cruz from publicly available sequence data; collaborators worldwide provide the rest. Users can stably add their own custom tracks to the browser for educational or research purposes. The conceptual and technical framework of the browser, its underlying MYSQL database, and overall use are described. The web site currently serves over 50,000 pages per day to over 3000 different users.
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                Author and article information

                Contributors
                jean-madeleine.desainteagathe@aphp.fr
                Journal
                Hum Genomics
                Hum Genomics
                Human Genomics
                BioMed Central (London )
                1473-9542
                1479-7364
                10 February 2023
                10 February 2023
                2023
                : 17
                : 7
                Affiliations
                [1 ]GRID grid.462844.8, ISNI 0000 0001 2308 1657, Département de Génétique Médicale, Groupe Hospitalier Universitaire de la Pitié Salpêtrière, AP-HP.Sorbonne Université, , Laboratoire de Médecine Génomique Sorbonne Université, ; Paris, France
                [2 ]Laboratoire de Biologie Médicale Multi-Sites SeqOIA (laboratoire-seqoia.fr/), Paris, France
                [3 ]GRID grid.277151.7, ISNI 0000 0004 0472 0371, Nantes Université, CHU Nantes, Service de Génétique Médicale, ; 44000 Nantes, France
                [4 ]GRID grid.411167.4, ISNI 0000 0004 1765 1600, Service de Génétique, Inserm U1253, , CHRU de Tours, ; Tours, France
                [5 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, Laboratoire de Génétique Moléculaire, , CHU de Montpellier, Université de Montpellier, ; Montpellier, France
                [6 ]GRID grid.411784.f, ISNI 0000 0001 0274 3893, Service de Médecine Génomique, Maladies de Système et d’Organe, Fédération de Génétique et de Médecine Génomique, DMU BioPhyGen, , APHP Centre-Université Paris Cité, Hôpital Cochin, ; Paris, France
                [7 ]GRID grid.411439.a, ISNI 0000 0001 2150 9058, Centre de référence des maladies neuromusculaires Nord/Est/Ile de France, , Hôpital Pitié-Salpêtrière, APHP, ; Paris, France
                [8 ]GRID grid.450308.a, ISNI 0000 0004 0369 268X, Inserm, U1216, CHU Grenoble Alpes, Grenoble Institut Neurosciences, , Université Grenoble Alpes, ; Grenoble, France
                [9 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, PhyMedExp, INSERM, CNRS, , Université de Montpellier, ; Montpellier, France
                [10 ]GRID grid.503422.2, ISNI 0000 0001 2242 6780, Centre mémoire, Inserm U1172 DistALZ, Licend, , Univ Lille, CHU Lille, ; 59000 Lille, France
                [11 ]GRID grid.121334.6, ISNI 0000 0001 2097 0141, INM, , Univ Montpellier, INSERM, ; Montpellier, France
                [12 ]GRID grid.157868.5, ISNI 0000 0000 9961 060X, INM, , Univ Montpellier, INSERM, CHU Montpellier, ; Montpellier, France
                Article
                451
                10.1186/s40246-023-00451-1
                9912651
                36765386
                8f626519-76a8-4985-9b41-5f0d1ff496f3
                © The Author(s) 2023

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 1 December 2022
                : 18 January 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100004923, AFM-Téléthon;
                Award ID: 21384
                Award Recipient :
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                © The Author(s) 2023

                Genetics
                Genetics

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