Evidence map›Paper›PMID 21121054›Full record

ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2011

Visual integration of results from a large DNA biobank (BioVU) using synthesis-view.

Sarah Pendergrass, Scott M Dudek, Dan M Roden, Dana C Crawford, Marylyn D Ritchie

Abstract read
In one paragraph

Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. A framework for understanding selection bias in real-world healthcare data.Journal of the Royal Statistical Society. Series A, (Statistics in Society) · 2024
    Article
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  7. KIDNEY DISEASE GENETICS AND THE IMPORTANCE OF DIVERSITY IN PRECISION MEDICINE.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2016
    Article
  8. Article
  9. Secondary use of clinical data: the Vanderbilt approach.Journal of biomedical informatics · 2014
    Article
  10. Article
  11. Article
  12. Article
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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

5 authors.

Sarah PendergrassCenter for Human Genetics Research, Department of Molecular Physiology and Biophysics, Vanderbilt University, 507D Light Hall, Nashville, TN 37205, USA. sarah.a.pendergrass@vanderbilt.edu
Scott M Dudek
Dan M Roden
Dana C Crawford
Marylyn D Ritchie

Funding

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
Epidemiologic Architecture for Genes Linked to Environment (EAGLE)U01HG004798 · NHGRI · VANDERBILT UNIVERSITY · PI CRAWFORD, DANA C · 2008 to 2013
$8.8M
Analysis Tool for Heritable and Envirnonmental Network AssociationsR01LM010040 · NLM · VANDERBILT UNIVERSITY · PI RITCHIE, MARYLYN D · 2009 to 2010
$1.9M
NHGRI NIH HHS HG004798NHGRI NIH HHS U01 HG004798NHLBI NIH HHS HL065962NHLBI NIH HHS U01 HL065962NHLBI NIH HHS U19 HL065962NLM NIH HHS LM010040NLM NIH HHS R01 LM010040
6 · The paper itself

Abstract

In this paper, we describe using Synthesis-View, a new method of presenting complex genetic data, to revisit results of a study from the BioVU Vanderbilt DNA databank. BioVU is a biorepository of DNA samples coupled with de-identified electronic medical records (EMR). In the Ritchie et al. study ~10,000 BioVU samples were genotyped for 21 SNPs that were previously associated with 5 diseases: atrial fibrillation, Crohn Disease, multiple sclerosis, rheumatoid arthritis, and type 2 diabetes. In the proof-of-concept study, the 21 tests of association replicated previous findings where sample size provided adequate power. The majority of the BioVU results were originally presented in tabular form. Herein we have revisited the results of this study using Synthesis-View. The Synthesis-View software tool visually synthesizes the results of complex, multi-layered studies that aim to characterize associations between small numbers of single-nucleotide polymorphisms (SNPs) and diseases and/or phenotypes, such as the results of replication and meta-analysis studies. Using Synthesis-View with the data of the Ritchie et al. study and presenting these data in this integrated visual format demonstrates new ways to investigate and interpret these kinds of data. Synthesis-View is freely available for non-commercial research institutions, for full details see https://chgr.mc.vanderbilt.edu/synthesisview.

Indexed as

SoftwareAlgorithmsComputational BiologyComputer GraphicsDatabases, Nucleic AcidDiseaseGenetic Association StudiesGenome-Wide Association StudyHumansPolymorphism, Single Nucleotide

Identifiers

PMID21121054
PMCPMC3065108

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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 OpenQuestion graph.