Evidence map›Paper›PMID 31135886›Full record

ArticleBiostatistics (Oxford, England)2021

The functional false discovery rate with applications to genomics.

Xiongzhi Chen, David G Robinson, John D Storey

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

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

  1. Polygenic Risk and Nutrient Intake Interactions on Obesity Outcomes: A Systematic Review and Meta-Analysis of Observational Studies.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Pooled it
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  18. Identification of potential molecular mechanisms and candidate drugs for radiotherapy- and chemotherapy-induced mucositis.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
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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

3 authors.

Xiongzhi ChenLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
David G RobinsonLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.
John D StoreyLewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ 08544, USA.

Funding

Quantitavie and Computational Biology Graduate ProgramT32HG003284 · NHGRI · PRINCETON UNIVERSITY · PI Joshua Michael Akey, Stanislav Y. Shvartsman · 2004 to 2026
$9.9M
Models and Methods for Population GenomicsR01HG006448 · NHGRI · PRINCETON UNIVERSITY · PI STOREY, JOHN D · 2012 to 2025
$3.8M
Statistical Methods for High-Throughput Gene Expression ProfilingR01HG002913 · NHGRI · UNIVERSITY OF WASHINGTON · PI STOREY, JOHN D · 2004 to 2015
$3.1M
NHGRI NIH HHS R01 HG002913NHGRI NIH HHS R01 HG006448NHGRI NIH HHS T32 HG003284
6 · The paper itself

Abstract

The false discovery rate (FDR) measures the proportion of false discoveries among a set of hypothesis tests called significant. This quantity is typically estimated based on p-values or test statistics. In some scenarios, there is additional information available that may be used to more accurately estimate the FDR. We develop a new framework for formulating and estimating FDRs and q-values when an additional piece of information, which we call an "informative variable", is available. For a given test, the informative variable provides information about the prior probability a null hypothesis is true or the power of that particular test. The FDR is then treated as a function of this informative variable. We consider two applications in genomics. Our first application is a genetics of gene expression (eQTL) experiment in yeast where every genetic marker and gene expression trait pair are tested for associations. The informative variable in this case is the distance between each genetic marker and gene. Our second application is to detect differentially expressed genes in an RNA-seq study carried out in mice. The informative variable in this study is the per-gene read depth. The framework we develop is quite general, and it should be useful in a broad range of scientific applications.

Indexed as

Genetic MarkersGenomicsAnimalsGene Expression ProfilingMiceProbabilitySaccharomyces cerevisiaeGenetic MarkerseQTLFDRFunctional data analysisGenetics of gene expressionKernel density estimationLocal false discovery rateMultiple hypothesis testingq-valueRNA-seqSequencing depth

Identifiers

PMID31135886
PMCPMC7846131

What OpenQuestion holds

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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.