Evidence map›Paper›PMID 39764392›Full record

ArticleArXiv2024

GREGoR: Accelerating Genomics for Rare Diseases.

Moez Dawood, Ben Heavner, Marsha M Wheeler, Rachel A Ungar, Jonathan LoTempio, Laurens Wiel, Seth Berger, Jonathan A Bernstein, Jessica X Chong, Emmanuèle C Délot and 23 more

Abstract readPreprint
In one paragraph

Article in ArXiv, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors.

Moez DawoodHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Ben HeavnerDepartment of Biostatistics, University of Washington, Seattle, WA, USA.
Marsha M WheelerDepartment of Biostatistics, University of Washington, Seattle, WA, USA.
Rachel A UngarDepartment of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
Jonathan LoTempioInstitute for Clinical and Translational Science, University of California, Irvine, CA, USA.
Laurens WielDepartment of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
Seth BergerDivision of Genetics and Metabolism, Children's National Rare Disease Institute, Washington, DC, USA.
Jonathan A BernsteinDepartment of Pediatrics, School of Medicine, Stanford University, Stanford, CA, USA.
Jessica X ChongDepartment of Pediatrics, Dvision of Genetic Medicine, University of Washington, Seattle, WA, USA.
Emmanuèle C DélotInstitute for Clinical and Translational Science, University of California, Irvine, CA, USA.
Evan E EichlerBrotman Baty Institute for Precision Medicine, University of Washington, Seattle, WA, USA.
Richard A GibbsHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
James R LupskiHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Ali ShojaieDepartment of Biostatistics, University of Washington, Seattle, WA, USA.
Michael E TalkowskiCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Alex H WagnerSteve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.
Chia-Lin WeiDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Christopher WellingtonOffice of Genomic Data Science, National Human Genome Research Institute, Bethesda, MD, USA.
Matthew T WheelerDivision of Cardiovascular Medicine, School of Medicine, Stanford University, Stanford, CA, USA.
GREGoR Partner Members
Claudia M B CarvalhoPacific Northwest Research Institute, Seattle, WA, USA.
Casey A GiffordDepartment of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
Susanne MayDepartment of Biostatistics, University of Washington, Seattle, WA, USA.
Danny E MillerBrotman Baty Institute for Precision Medicine, University of Washington, Seattle, WA, USA.
Heidi L RehmCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Fritz J SedlazeckHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Eric VilainInstitute for Clinical and Translational Science, University of California, Irvine, CA, USA.
Anne O'Donnell-LuriaCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Jennifer E PoseyDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Lisa H ChadwickDivision of Genome Sciences, National Human Genome Research Institute, Bethesda, MD, USA.
Michael J BamshadDepartment of Pediatrics, Dvision of Genetic Medicine, University of Washington, Seattle, WA, USA.
Stephen B MontgomeryDepartment of Genetics, School of Medicine, Stanford University, Stanford, CA, USA.
Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium

Funding

Stanford Mendelian Genomics Research CenterU01HG011762 · NHGRI · STANFORD UNIVERSITY · PI Jonathan Adam Bernstein, Stephen Montgomery · 2021 to 2026
$16.7M
University of Washington Mendelian Genomics Research Center (UW-MGRC)U01HG011744 · NHGRI · UNIVERSITY OF WASHINGTON · PI MICHAEL Joseph BAMSHAD, Evan Eichler · 2021 to 2026
$15.8M
University of Washington (UW) Mendelian Genomics Data Coordinating CenterU24HG011746 · NHGRI · UNIVERSITY OF WASHINGTON · PI Susanne May, ALI SHOJAIE · 2021 to 2026
$14.8M
Broad Institute Mendelian Genomic Research CenterU01HG011755 · NHGRI · BROAD INSTITUTE, INC. · PI Anne O'Donnell-Luria, MICHAEL E TALKOWSKI · 2021 to 2026
$14.6M
Frequency of variants of unknown significance by ancestry groups in the All of Us Research Program cohortU01HG011758 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI RICHARD A GIBBS, JAMES R. LUPSKI · 2021 to 2026
$13.8M
Pediatric Mendelian Genomics Research CenterU01HG011745 · NHGRI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Eric J. Vilain · 2021 to 2026
$13.3M
Clinical Diagnostic Sequencing of Structural VariationR01HD081256 · NICHD · MASSACHUSETTS GENERAL HOSPITAL · PI TALKOWSKI, MICHAEL E · 2015 to 2025
$7.2M
Evaluating the Impact of Mutations in Distant-Acting Enhancers in Structural Birth DefectsR01HD114353 · NICHD · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI Len Alexander Pennacchio, Axel Visel · 2023 to 2026
$3.3M
Center for Undiagnosed Diseases at StanfordU01NS134358 · NINDS · STANFORD UNIVERSITY · PI Jonathan Adam Bernstein, HOLLY K TABOR · 2023 to 2026
$3.1M
NHGRI NIH HHS U01 HG011744NHGRI NIH HHS U01 HG011745NHGRI NIH HHS U01 HG011755NHGRI NIH HHS U01 HG011758NHGRI NIH HHS U01 HG011762NHGRI NIH HHS U24 HG011746NICHD NIH HHS R01 HD081256NICHD NIH HHS R01 HD114353NINDS NIH HHS U01 NS134358
6 · The paper itself

Abstract

Rare diseases are collectively common, affecting approximately one in twenty individuals worldwide. In recent years, rapid progress has been made in rare disease diagnostics due to advances in DNA sequencing, development of new computational and experimental approaches to prioritize genes and genetic variants, and increased global exchange of clinical and genetic data. However, more than half of individuals suspected to have a rare disease lack a genetic diagnosis. The Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium was initiated to study thousands of challenging rare disease cases and families and apply, standardize, and evaluate emerging genomics technologies and analytics to accelerate their adoption in clinical practice. Further, all data generated, currently representing ~7500 individuals from ~3000 families, is rapidly made available to researchers worldwide via the Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL) to catalyze global efforts to develop approaches for genetic diagnoses in rare diseases (https://gregorconsortium.org/data). The majority of these families have undergone prior clinical genetic testing but remained unsolved, with most being exome-negative. Here, we describe the collaborative research framework, datasets, and discoveries comprising GREGoR that will provide foundational resources and substrates for the future of rare disease genomics.

Identifiers

PMID39764392
PMCPMC11702807

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.