Evidence map›Paper›PMID 29079728›Full record

ArticleNature communications2017

PLATO software provides analytic framework for investigating complexity beyond genome-wide association studies.

Molly A Hall, John Wallace, Anastasia Lucas, Dokyoon Kim, Anna O Basile, Shefali S Verma, Cathy A McCarty, Murray H Brilliant, Peggy L Peissig, Terrie E Kitchner and 5 more

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
–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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Influence of tissue context on gene prioritization for predicted transcriptome-wide association studies.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2019
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  20. Leveraging putative enhancer-promoter interactions to investigate two-way epistasis in Type 2 Diabetes GWAS.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2018
    Article
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

15 authors.

Molly A HallInstitute for Biomedical Informatics, Departments of Genetics and Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
John WallaceBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Anastasia LucasBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Dokyoon KimBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Anna O BasileDepartment of Biochemistry and Molecular Biology, Center for Systems Genomics, Eberly College of Science, The Pennsylvania State University, University Park, PA, 16802, USA.
Shefali S VermaBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Cathy A McCartyEssentia Institute of Rural Health, Duluth, MN, 55805, USA.
Murray H BrilliantMarshfield Clinic Research Institute, Marshfield, WI, 54449, USA.
Peggy L PeissigMarshfield Clinic Research Institute, Marshfield, WI, 54449, USA.
Terrie E KitchnerMarshfield Clinic Research Institute, Marshfield, WI, 54449, USA.
Anurag VermaBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Sarah A PendergrassBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Scott M DudekBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA.
Jason H MooreInstitute for Biomedical Informatics, Departments of Genetics and Biostatistics and Epidemiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Marylyn D RitchieBiomedical and Translational Informatics Institute, Geisinger Health System, Danville, PA, 17821, USA. mdritchie@geisinger.edu.ORCID http://orcid.org/0000-0002-1208-1720

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI A. Clementina Mesaros · 2006 to 2026
$35.3M
Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
PHARMACOGENOMICS OF ARRHYTHMIA THERAPYU01HL065962 · NHLBI · VANDERBILT UNIVERSITY · PI RODEN, DAN M · 2001 to 2009
$24.8M
Pharmacogenomics of Arrhythmia TherapyU19HL065962 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RODEN, DAN M · 2010 to 2014
$17.4M
eMERGE Coordinating Center - Administrative SupplementU01HG006385 · NHGRI · VANDERBILT UNIVERSITY · PI HARRIS, PAUL A. · 2011 to 2014
$5.4M
Bioinformatics Strategies for Genome-Wide Association StudiesR01LM010098 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H., WILLIAMS, SCOTT MATTHEW · 2009 to 2023
$5.1M
IRIS: Incorporating Research Into SightU01HG006389 · NHGRI · ESSENTIA INSTITUTE OF RURAL HEALTH · PI MCCARTY, CATHERINE ANNE · 2011 to 2014
$4.1M
Machine Learning Prediction of Cancer SusceptibilityR01LM009012 · NLM · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H. · 2006 to 2014
$3.3M
Biomedical Computing and Informatics Strategies for Infectious Disease ResearchR01AI116794 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI MOORE, JASON H. · 2016 to 2020
$2.9M
Analysis Tool for Heritable and Envirnonmental Network AssociationsR01LM010040 · NLM · VANDERBILT UNIVERSITY · PI RITCHIE, MARYLYN D · 2009 to 2010
$1.9M
Penn State Biomedical Big Data to Knowledge (B2D2K) Training ProgramT32LM012415 · NLM · PENNSYLVANIA STATE UNIVERSITY, THE · PI BROACH, JAMES R., HONAVAR, VASANT G. · 2016 to 2020
$1.2M
Novel methods to identify and replicate complex interactions in common diseaseF31HG008588 · NHGRI · PENNSYLVANIA STATE UNIVERSITY, THE · PI HALL, MOLLY ANN · 2015 to 2015
$9k
NCATS NIH HHS UL1 TR000427NHGRI NIH HHS F31 HG008588NHGRI NIH HHS U01 HG006385NHGRI NIH HHS U01 HG006389NHLBI NIH HHS U01 HL065962NHLBI NIH HHS U19 HL065962NIAID NIH HHS R01 AI116794NIEHS NIH HHS P30 ES013508NLM NIH HHS R01 LM009012NLM NIH HHS R01 LM010040NLM NIH HHS R01 LM010098NLM NIH HHS T32 LM012415
6 · The paper itself

Abstract

Genome-wide, imputed, sequence, and structural data are now available for exceedingly large sample sizes. The needs for data management, handling population structure and related samples, and performing associations have largely been met. However, the infrastructure to support analyses involving complexity beyond genome-wide association studies is not standardized or centralized. We provide the PLatform for the Analysis, Translation, and Organization of large-scale data (PLATO), a software tool equipped to handle multi-omic data for hundreds of thousands of samples to explore complexity using genetic interactions, environment-wide association studies and gene-environment interactions, phenome-wide association studies, as well as copy number and rare variant analyses. Using the data from the Marshfield Personalized Medicine Research Project, a site in the electronic Medical Records and Genomics Network, we apply each feature of PLATO to type 2 diabetes and demonstrate how PLATO can be used to uncover the complex etiology of common traits.

Indexed as

Computational BiologyGenome, HumanGenome-Wide Association StudyAlcohol DrinkingAllelesDatabases, GeneticDiabetes Mellitus, Type 2DietEpistasis, GeneticGene DeletionGene DosageGene-Environment InteractionGenomicsGenotypeGlutamate DecarboxylaseHumansGlutamate Decarboxylaseglutamate decarboxylase 1glutamate decarboxylase 2

Identifiers

PMID29079728
PMCPMC5660079

What OpenQuestion 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 OpenQuestion graph.