Evidence map›Paper›PMID 30217148›Full record

ArticleBMC bioinformatics2018

Using controls to limit false discovery in the era of big data.

Matthew M Parks, Benjamin J Raphael, Charles E Lawrence

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Article
  3. 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

3 authors.

Matthew M ParksDepartment of Physiology and Biophysics, Weill Cornell Medicine, 1300 York Ave, New York, NY, 10065, USA.
Benjamin J RaphaelDepartment of Computer Science, Princeton University, 35 Olden Street, Princeton, NJ, 08540, USA.
Charles E LawrenceCenter for Computational Molecular Biology, Brown University, 115 Waterman Street, Providence, RI, 02912, USA. charles_lawrence@brown.edu.ORCID http://orcid.org/0000-0003-4011-6692

Funding

Computational Approaches for Structural Variation Studies in GenomesR01HG005690 · NHGRI · BROWN UNIVERSITY · PI RAPHAEL, BENJAMIN · 2011 to 2015
$2.4M
Directorate for Mathematical and Physical Sciences CCF-1053753National Human Genome Research Institute R01HG5690NHGRI NIH HHS R01 HG005690
6 · The paper itself

Abstract

backgroundProcedures for controlling the false discovery rate (FDR) are widely applied as a solution to the multiple comparisons problem of high-dimensional statistics. Current FDR-controlling procedures require accurately calculated p-values and rely on extrapolation into the unknown and unobserved tails of the null distribution. Both of these intermediate steps are challenging and can compromise the reliability of the results.

resultsWe present a general method for controlling the FDR that capitalizes on the large amount of control data often found in big data studies to avoid these frequently problematic intermediate steps. The method utilizes control data to empirically construct the distribution of the test statistic under the null hypothesis and directly compares this distribution to the empirical distribution of the test data. By not relying on p-values, our control data-based empirical FDR procedure more closely follows the foundational principles of the scientific method: that inference is drawn by comparing test data to control data. The method is demonstrated through application to a problem in structural genomics.

conclusionsThe method described here provides a general statistical framework for controlling the FDR that is specifically tailored for the big data setting. By relying on empirically constructed distributions and control data, it forgoes potentially problematic modeling steps and extrapolation into the unknown tails of the null distribution. This procedure is broadly applicable insofar as controlled experiments or internal negative controls are available, as is increasingly common in the big data setting.

Indexed as

Models, StatisticalBayes TheoremDatabases, FactualDNA RepairGenome, HumanHumansBig dataFalse discovery rate (FDR)High dimensional inferenceHypothesis testing

Identifiers

PMID30217148
PMCPMC6137876

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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.