Evidence map›Paper›PMID 37279733›Full record

ArticleBioinformatics (Oxford, England)2023

JUMP: replicability analysis of high-throughput experiments with applications to spatial transcriptomic studies.

Pengfei Lyu, Yan Li, Xiaoquan Wen, Hongyuan Cao

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Pengfei LyuDepartment of Statistics, Florida State University, 600 W College AVE, Tallahassee, FL 32306, United States.
Yan LiSchool of Mathematics, Jilin University, 2699 Qianjin ST, Changchun, Jilin 130012, China.ORCID 0000-0002-1612-5719
Xiaoquan WenDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109, United States.ORCID 0000-0001-8990-2737
Hongyuan CaoDepartment of Statistics, Florida State University, 600 W College AVE, Tallahassee, FL 32306, United States.

Funding

Resolving Methodological Challenges in Genomics Research: Causality, Risk Prediction, and Reproducibility: Administrative SupplementR35GM138121 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Xiaoquan Wen · 2020 to 2026
$2.4M
NIGMS NIH HHS R35 GM138121
6 · The paper itself

Abstract

motivationReplicability is the cornerstone of scientific research. The current statistical method for high-dimensional replicability analysis either cannot control the false discovery rate (FDR) or is too conservative.

resultsWe propose a statistical method, JUMP, for the high-dimensional replicability analysis of two studies. The input is a high-dimensional paired sequence of p-values from two studies and the test statistic is the maximum of p-values of the pair. JUMP uses four states of the p-value pairs to indicate whether they are null or non-null. Conditional on the hidden states, JUMP computes the cumulative distribution function of the maximum of p-values for each state to conservatively approximate the probability of rejection under the composite null of replicability. JUMP estimates unknown parameters and uses a step-up procedure to control FDR. By incorporating different states of composite null, JUMP achieves a substantial power gain over existing methods while controlling the FDR. Analyzing two pairs of spatially resolved transcriptomic datasets, JUMP makes biological discoveries that otherwise cannot be obtained by using existing methods. AVAILABILITY AND IMPLEMENTATION: An R package JUMP implementing the JUMP method is available on CRAN (https://CRAN.R-project.org/package=JUMP).

Indexed as

Gene Expression ProfilingTranscriptome

Identifiers

PMID37279733
PMCPMC10279524

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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.