Evidence map›Paper›PMID 38962029›Full record

ArticleNEJM AI2024

AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders.

Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill A Rosenfeld, Linyan Meng and 14 more

Abstract read
In one paragraph

Article in NEJM AI, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Dongxue MaoDepartment of Pediatrics, Baylor College of Medicine, Houston.ORCID 0000-0002-8443-2833
Chaozhong LiuJan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston.ORCID 0000-0002-6960-1977
Linhua WangJan and Dan Duncan Neurological Research Institute at Texas Children's Hospital, Houston.ORCID 0000-0002-6717-860X
Rami Ai-OuranDepartment of Pediatrics, Baylor College of Medicine, Houston.ORCID 0009-0004-6255-4727
Cole DeisserothDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-9097-1617
Sasidhar PasupuletiDepartment of Pediatrics, Baylor College of Medicine, Houston.ORCID 0000-0003-0310-5812
Seon Young KimDepartment of Pediatrics, Baylor College of Medicine, Houston.ORCID 0009-0003-7542-545X
Lucian LiDepartment of Pediatrics, Baylor College of Medicine, Houston.ORCID 0000-0002-9462-6527
Jill A RosenfeldDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-5664-7987
Linyan MengDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-7474-9178
Lindsay C BurrageDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0002-5108-8861
Michael F WanglerDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-5245-5910
Shinya YamamotoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0003-2172-8036
Undiagnosed Diseases Network
Michael SantanaBaylor Genetics, Houston7.ORCID 0009-0002-3209-1229
Victor PerezBaylor Genetics, Houston7.ORCID 0009-0006-6660-7907
Priyank ShuklaBaylor Genetics, Houston7.ORCID 0009-0001-9308-1465
Christine M EngDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0009-0008-8627-8228
Brendan LeeDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-8573-4211
Bo YuanDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-7278-5116
Fan XiaDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0002-4974-9851
Hugo J BellenDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0001-5992-5989
Pengfei LiuDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston.ORCID 0000-0002-4177-709X
Zhandong LiuDepartment of Pediatrics, Baylor College of Medicine, Houston.ORCID 0000-0002-7608-0831

Funding

Coordinating Center for the Undiagnosed Diseases NetworkU01HG007530 · NHGRI · HARVARD MEDICAL SCHOOL · PI KOHANE, ISAAC S. · 2014 to 2022
$30.2M
Pilot of New Technologies to Increase the Genomic Diagnosis of Undiagnosed Disease Network (UDN) PatientsU01HG007709 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI BACINO, CARLOS A., LEE, BRENDAN · 2014 to 2022
$14.3M
Vanderbilt Center for Undiagnosed Diseases (VCUD) - BiorepositoryU01HG007674 · NHGRI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI COGAN, JOY D, HAMID, RIZWAN · 2014 to 2022
$13.7M
An integrated and diverse genomic medicine program for undiagnosed diseasesU01HG007672 · NHGRI · DUKE UNIVERSITY · PI SHASHI, VANDANA · 2014 to 2022
$13.4M
Clinical Sequencing Core Facility for the Undiagnosed Diseases Network (UDN)U01HG007942 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI ENG, CHRISTINE · 2014 to 2021
$10.2M
UCLA clinical site for the investigation of undiagnosed disordersU01HG007703 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MARTINEZ-AGOSTO, JULIAN, NELSON, STANLEY F. · 2014 to 2022
$10.1M
Preclinical and Clincial OutcomesP50HD103555 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI MIRJANA MALETIC-SAVATIC · 2020 to 2026
$9.9M
Stanford Center for Undiagnosed DiseasesU01HG007708 · NHGRI · STANFORD UNIVERSITY · PI ASHLEY, EUAN A, BERNSTEIN, JONATHAN ADAM · 2014 to 2018
$8.0M
Zebrafish CoreU54NS093793 · NINDS · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J · 2015 to 2022
$7.5M
What comes next? Engaging stakeholders in governance of participant data and relationships during the sunset of large genomic medicine research initiativesU01HG010218 · NHGRI · STANFORD UNIVERSITY · PI ASHLEY, EUAN A, BERNSTEIN, JONATHAN ADAM · 2018 to 2022
$6.3M
Genomic medicine and gene function implementation for an underserved populationR01HG011795 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI BELLEN, HUGO J, WANGLER, MICHAEL FRANCIS · 2021 to 2025
$4.8M
Clinical Genome Wide Sequencing Core for the Undiagnosed Disease NetworkU01HG007943 · NHGRI · MEDICAL COLLEGE OF WISCONSIN · PI WORTHEY, ELIZABETH A · 2014 to 2017
$4.1M
NHGRI NIH HHS R01 HG011795NHGRI NIH HHS R35 HG011311NHGRI NIH HHS U01 HG007530NHGRI NIH HHS U01 HG007672NHGRI NIH HHS U01 HG007674NHGRI NIH HHS U01 HG007703NHGRI NIH HHS U01 HG007708NHGRI NIH HHS U01 HG007709NHGRI NIH HHS U01 HG007942NHGRI NIH HHS U01 HG007943NHGRI NIH HHS U01 HG010218NICHD NIH HHS P50 HD103555NINDS NIH HHS U54 NS093793
6 · The paper itself

Abstract

backgroundDiagnosing genetic disorders requires extensive manual curation and interpretation of candidate variants, a labor-intensive task even for trained geneticists. Although artificial intelligence (AI) shows promise in aiding these diagnoses, existing AI tools have only achieved moderate success for primary diagnosis.

methodsAI-MARRVEL (AIM) uses a random-forest machine-learning classifier trained on over 3.5 million variants from thousands of diagnosed cases. AIM additionally incorporates expert-engineered features into training to recapitulate the intricate decision-making processes in molecular diagnosis. The online version of AIM is available at https://ai.marrvel.org. To evaluate AIM, we benchmarked it with diagnosed patients from three independent cohorts.

resultsAIM improved the rate of accurate genetic diagnosis, doubling the number of solved cases as compared with benchmarked methods, across three distinct real-world cohorts. To better identify diagnosable cases from the unsolved pools accumulated over time, we designed a confidence metric on which AIM achieved a precision rate of 98% and identified 57% of diagnosable cases out of a collection of 871 cases. Furthermore, AIM's performance improved after being fine-tuned for targeted settings including recessive disorders and trio analysis. Finally, AIM demonstrated potential for novel disease gene discovery by correctly predicting two newly reported disease genes from the Undiagnosed Diseases Network.

conclusionsAIM achieved superior accuracy compared with existing methods for genetic diagnosis. We anticipate that this tool may aid in primary diagnosis, reanalysis of unsolved cases, and the discovery of novel disease genes. (Funded by the NIH Common Fund and others.).

Identifiers

PMID38962029
PMCPMC11221788

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.