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Record W4405173050 · doi:10.1016/j.gim.2024.101336

Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing data sets

2024· article· en· W4405173050 on OpenAlexafffund
Ben Weisburd, Rakshya Sharma, Villem Pata, Tiia Reimand, Vijay S Ganesh, Christina Austin‐Tse, Ikeoluwa Osei‐Owusu, Emily O’Heir, Melanie O’Leary, Lynn Pais, Seth A. Stafki, Audrey L. Daugherty, Chiara Folland, Stojan Perić, Nagia Fahmy, Bjarne Udd, Magda Horáková, Anna Łusakowska, Rohan Manoj, Atchayaram Nalini, Veronika Karcagi, Kiran Polavarapu, Hanns Lochmüller, Rita Horváth, Carsten G. Bönnemann, Sandra Donkervoort, Göknur Haliloğlu, Özlem Hergüner, Peter B. Kang, Gianina Ravenscroft, Nigel G. Laing, Hamish S. Scott, Ana Töpf, Volker Straub, Sander Pajusalu, Katrin Õunap, Grace Tiao, Heidi L. Rehm, Anne O’Donnell‐Luria

Bibliographic record

VenueGenetics in Medicine · 2024
Typearticle
Languageen
FieldMedicine
TopicNeurogenetic and Muscular Disorders Research
Canadian institutionsChildren's Hospital of Eastern Ontario
FundersMemphis Research ConsortiumH2020 Marie Skłodowska-Curie ActionsNational Institute of Neurological Disorders and StrokeNational Heart, Lung, and Blood InstituteNIHR Cambridge Biomedical Research CentreUCLH Biomedical Research CentreHORIZON EUROPE Framework ProgrammeLGMD2D FoundationSanofi GenzymeNational Eye InstituteEesti TeadusagentuurNational Institutes of HealthCanada First Research Excellence FundCanada Research ChairsMedical Research CouncilAtaxia UKNational Institute for Health and Care ResearchHorizon TherapeuticsKurt+Peter FoundationUK Research and InnovationLimb Girdle Muscular Dystrophy 2ILifeArcEuropean CommissionNational Institute of Arthritis and Musculoskeletal and Skin DiseasesGovernment of CanadaSanofiSilicon Valley Community FoundationMuscular Dystrophy UKMinistry of HealthChan Zuckerberg InitiativeWellcome TrustCanada Foundation for InnovationCanadian Institutes of Health ResearchLimb Girdle Muscular Dystrophy 2i Research FundNational Human Genome Research InstituteUltragenyx Pharmaceutical
KeywordsSpinal muscular atrophyExome sequencingExomeMedicineGenomeBioinformaticsAtrophyComputational biologyPathologyGeneticsBiologyMutationGeneDisease

Abstract

fetched live from OpenAlex

PURPOSE: We set out to develop a publicly available tool that could accurately diagnose spinal muscular atrophy (SMA) in exome, genome, or panel sequencing data sets aligned to a GRCh37, GRCh38, or T2T reference genome. METHODS: The SMA Finder algorithm detects the most common genetic causes of SMA by evaluating reads that overlap the c.840 position of the SMN1 and SMN2 paralogs. It uses these reads to determine whether an individual most likely has 0 functional copies of SMN1. RESULTS: We developed SMA Finder and evaluated it on 16,626 exomes and 3911 genomes from the Broad Institute Center for Mendelian Genomics, 1157 exomes and 8762 panel samples from Tartu University Hospital, and 198,868 exomes and 198,868 genomes from the UK Biobank. SMA Finder's false-positive rate was below 1 in 200,000 samples, its positive predictive value was greater than 96%, and its true-positive rate was 29 out of 29. Most of these SMA diagnoses had initially been clinically misdiagnosed as limb-girdle muscular dystrophy. CONCLUSION: Our extensive evaluation of SMA Finder on exome, genome, and panel sequencing samples found it to have nearly 100% accuracy and demonstrated its ability to reduce diagnostic delays, particularly in individuals with milder subtypes of SMA. Given this accuracy, the common misdiagnoses identified here, the widespread availability of clinical confirmatory testing for SMA, and the existence of treatment options, we propose that it is time to add SMN1 to the American College of Medical Genetics list of genes with reportable secondary findings after genome and exome sequencing.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.729
Threshold uncertainty score0.630

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.213
GPT teacher head0.403
Teacher spread0.189 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations5
Published2024
Admission routes2
Has abstractyes

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