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

被引:68
作者
Agathe, Jean-Madeleine de Sainte [1 ,2 ]
Filser, Mathilde [1 ]
Isidor, Bertrand [3 ]
Besnard, Thomas [3 ]
Gueguen, Paul [2 ,4 ]
Perrin, Aurelien [5 ]
Van Goethem, Charles [5 ]
Verebi, Camille [6 ]
Masingue, Marion [7 ]
Rendu, John [8 ]
Cossee, Mireille [5 ,9 ]
Bergougnoux, Anne [5 ,9 ]
Frobert, Laurent [2 ]
Buratti, Julien [1 ]
Lejeune, Elodie [1 ]
Le Guern, Eric [1 ,2 ]
Pasquier, Florence [10 ]
Clot, Fabienne [1 ]
Kalatzis, Vasiliki [11 ]
Roux, Anne-Francoise [5 ,12 ]
Cogne, Benjamin [2 ,3 ]
Baux, David [5 ,12 ]
机构
[1] Sorbonne Univ, Lab Medecine Genomique Sorbonne Univ, Dept Genet Medicale, AP HP,Grp Hospitalier Univ Pitie Salpetriere, Paris, France
[2] Lab Biol Medicale Multis SeqOIA Lab seqoia fr, Paris, France
[3] Nantes Univ, CHU Nantes, Serv Genet Medicale, F-44000 Nantes, France
[4] CHRU Tours, Serv Genet, Inserm U1253, Tours, France
[5] Univ Montpellier, CHU Montpellier, Lab Genet Mol, Montpellier, France
[6] Univ Paris Cite, Hop Cochin, APHP Ctr, DMU BioPhyGen,Serv Medecine Genomique ,Malad Syst, Paris, France
[7] Hop La Pitie Salpetriere, Ctr reference Malad neuromusculaires Nord Est Ile, APHP, Paris, France
[8] Univ Grenoble Alpes, Grenoble Inst Neurosci, Inserm, U1216,CHU Grenoble, Grenoble, France
[9] Univ Montpellier, PhyMedExp, INSERM, CNRS, Montpellier, France
[10] Univ Lille, Ctr memoire, Inserm DistALZ U1172, Licend,CHU Lille, F-59000 Lille, France
[11] Univ Montpellier, INM, INSERM, Montpellier, France
[12] Univ Montpellier, INM, INSERM, CHU Montpellier, Montpellier, France
关键词
GENE; MUTATIONS; FREQUENT; GENOMICS;
D O I
10.1186/s40246-023-00451-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 ().
引用
收藏
页数:16
相关论文
共 40 条
  • [1] Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion
    Abou Tayoun, Ahmad N.
    Pesaran, Tina
    DiStefano, Marina T.
    Oza, Andrea
    Rehm, Heidi L.
    Biesecker, Leslie G.
    Harrison, Steven M.
    [J]. HUMAN MUTATION, 2018, 39 (11) : 1517 - 1524
  • [2] MobiDetails: online DNA variants interpretation
    Baux, David
    Van Goethem, Charles
    Ardouin, Olivier
    Guignard, Thomas
    Bergougnoux, Anne
    Koenig, Michel
    Roux, Anne-Francoise
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2021, 29 (02) : 356 - 360
  • [3] Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants
    Bournazos, Adam M.
    Riley, Lisa G.
    Bommireddipalli, Shobhana
    Ades, Lesley
    Akesson, Lauren S.
    Al-Shinnag, Mohammad
    Alexander, Stephen, I
    Archibald, Alison D.
    Balasubramaniam, Shanti
    Berman, Yemima
    Beshay, Victoria
    Boggs, Kirsten
    Bojadzieva, Jasmina
    Brown, Natasha J.
    Bryen, Samantha J.
    Buckley, Michael F.
    Chong, Belinda
    Davis, Mark R.
    Dawes, Ruebena
    Delatycki, Martin
    Donaldson, Liz
    Downie, Lilian
    Edwards, Caitlin
    Edwards, Matthew
    Engel, Amanda
    Ewans, Lisa J.
    Faiz, Fathimath
    Fennell, Andrew
    Field, Michael
    Freckmann, Mary-Louise
    Gallacher, Lyndon
    Gear, Russell
    Goel, Himanshu
    Goh, Shuxiang
    Goodwin, Linda
    Hanna, Bernadette
    Harraway, James
    Higgins, Megan
    Ho, Gladys
    Hopper, Bruce K.
    Horton, Ari E.
    Hunter, Matthew F.
    Huq, Aamira J.
    Josephi-Taylor, Sarah
    Joshi, Himanshu
    Kirk, Edwin
    Krzesinski, Emma
    Kumar, Kishore R.
    Lemckert, Frances
    Leventer, Richard J.
    [J]. GENETICS IN MEDICINE, 2022, 24 (01) : 130 - 145
  • [4] Spectrum of pontocerebellar hypoplasia in 13 girls and boys with CASK mutations: confirmation of a recognizable phenotype and first description of a male mosaic patient
    Burglen, Lydie
    Chantot-Bastaraud, Sandra
    Garel, Catherine
    Milh, Mathieu
    Touraine, Renaud
    Zanni, Ginevra
    Petit, Florence
    Afenjar, Alexandra
    Goizet, Cyril
    Barresi, Sabina
    Coussement, Aurelie
    Ioos, Christine
    Lazaro, Leila
    Joriot, Sylvie
    Desguerre, Isabelle
    Lacombe, Didier
    des Portes, Vincent
    Bertini, Enrico
    Siffroi, Jean-Pierre
    de Villemeur, Thierry Billette
    Rodriguez, Diana
    [J]. ORPHANET JOURNAL OF RARE DISEASES, 2012, 7
  • [5] Functional Analysis of the PCCA and PCCB Gene Variants Predicted to Affect Splicing
    Bychkov, Igor
    Galushkin, Artur
    Filatova, Alexandra
    Nekrasov, Andrey
    Kurkina, Marina
    Baydakova, Galina
    Ilyushkina, Alexandra
    Skoblov, Mikhail
    Zakharova, Ekaterina
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (08)
  • [6] 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
    Cingolani, Pablo
    Platts, Adrian
    Wang, Le Lily
    Coon, Melissa
    Tung Nguyen
    Wang, Luan
    Land, Susan J.
    Lu, Xiangyi
    Ruden, Douglas M.
    [J]. FLY, 2012, 6 (02) : 80 - 92
  • [7] Interpretable prioritization of splice variants in diagnostic next-generation sequencing
    Danis, Daniel
    Jacobsen, Julius O. B.
    Carmody, Leigh C.
    Gargano, Michael A.
    McMurry, Julie A.
    Hegde, Ayushi
    Haendel, Melissa A.
    Valentini, Giorgio
    Smedley, Damian
    Robinson, Peter N.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2021, 108 (09) : 1564 - 1577
  • [8] Dawes R., 2021, NAT COMMUN, DOI [10.1101/2021.07.18.452855, DOI 10.1101/2021.07.18.452855]
  • [9] Empirical prediction of variant-activated cryptic splice donors using population-based RNA-Seq data
    Dawes, Ruebena
    Joshi, Himanshu
    Cooper, Sandra T.
    [J]. NATURE COMMUNICATIONS, 2022, 13 (01)
  • [10] An exon skipping-associated nonsense mutation in the dystrophin gene uncovers a complex interplay between multiple antagonistic splicing elements
    Disset, A
    Bourgeois, CF
    Benmalek, N
    Claustres, M
    Stevenin, J
    Tuffery-Giraud, S
    [J]. HUMAN MOLECULAR GENETICS, 2006, 15 (06) : 999 - 1013