Evidence map›Paper›PMID 32522875›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk.

Ronald Yurko, Max G'Sell, Kathryn Roeder, Bernie Devlin

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.9field-weighted citation impact, top 9% of its field
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

7 citing papers in PubMed, 17 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Ronald YurkoDepartment of Statistics & Data Science, Carnegie Mellon University, Pittsburgh, PA 15213.ORCID 0000-0001-9677-6599
Max G'SellDepartment of Statistics & Data Science, Carnegie Mellon University, Pittsburgh, PA 15213.
Kathryn RoederDepartment of Statistics & Data Science, Carnegie Mellon University, Pittsburgh, PA 15213; roeder@andrew.cmu.edu.ORCID 0000-0002-8869-6254
Bernie DevlinDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213.ORCID 0000-0003-2524-4290
Carnegie Mellon University · USUniversity of Pittsburgh · US

Funding

Genetics Association in Schizophrenia and Other DisordersR37MH057881 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DEVLIN, BERNIE · 2013 to 2022
$5.4M
NIMH NIH HHS R37 MH057881
6 · The paper itself

Abstract

To correct for a large number of hypothesis tests, most researchers rely on simple multiple testing corrections. Yet, new methodologies of selective inference could potentially improve power while retaining statistical guarantees, especially those that enable exploration of test statistics using auxiliary information (covariates) to weight hypothesis tests for association. We explore one such method, adaptive

Indexed as

AlgorithmsBipolar DisorderGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHumansMultifactorial InheritancePolymorphism, Single NucleotideQuantitative Trait LociSchizophreniaeQTLfalse discovery rateGWASmultiple hypothesis testingneuropsychiatric disorders

Identifiers

PMID32522875
PMCPMC7334489
OpenAlexW3033717297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.