Evidence map›Paper›PMID 33140829›Full record

ArticleGigaScience2020

Correcting for experiment-specific variability in expression compendia can remove underlying signals.

Alexandra J Lee, YoSon Park, Georgia Doing, Deborah A Hogan, Casey S Greene

Abstract read
In one paragraph

Article in GigaScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–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

15 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Evolutionary divergence ofRNA (New York, N.Y.) · 2022
    Article
  11. Article
  12. Ten quick tips for deep learning in biology.PLoS computational biology · 2022
    Article
  13. Using genome-wide expression compendia to study microorganisms.Computational and structural biotechnology journal · 2022
    Review
  14. Article
  15. 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

5 authors.

Alexandra J LeeGenomics and Computational Biology Graduate Program, University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA.
YoSon ParkDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA.
Georgia DoingDepartment of Microbiology and Immunology, Geisel School of Medicine, Dartmouth, 1 Rope Ferry Rd, Hanover, NH, 03755, USA.
Deborah A HoganDepartment of Microbiology and Immunology, Geisel School of Medicine, Dartmouth, 1 Rope Ferry Rd, Hanover, NH, 03755, USA.
Casey S GreeneDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA.

Funding

Molecular and Cellular Biology at DartmouthT32GM008704 · NIGMS · DARTMOUTH COLLEGE · PI COMPTON, DUANE A. · 1998 to 2018
$6.8M
Network-based algorithms for target identification and drug repositioning from genetic associationsR01HG010067 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI GREENE, CASEY S · 2018 to 2022
$3.2M
Characterization of high-grade serous ovarian cancer subtypes via single-cell profilingR01CA237170 · NCI · UNIVERSITY OF PENNSYLVANIA · PI DOHERTY, JENNIFER A., GREENE, CASEY S · 2019 to 2024
$3.0M
Characterizing Molecular Subtypes of Ovarian Cancer in African-American WomenR01CA200854 · NCI · UNIVERSITY OF UTAH · PI DOHERTY, JENNIFER A., SCHILDKRAUT, JOELLEN M. · 2016 to 2021
$2.8M
NCI NIH HHS R01 CA200854NCI NIH HHS R01 CA237170NHGRI NIH HHS R01 HG010067NIGMS NIH HHS T32 GM008704
6 · The paper itself

Abstract

motivationIn the past two decades, scientists in different laboratories have assayed gene expression from millions of samples. These experiments can be combined into compendia and analyzed collectively to extract novel biological patterns. Technical variability, or "batch effects," may result from combining samples collected and processed at different times and in different settings. Such variability may distort our ability to extract true underlying biological patterns. As more integrative analysis methods arise and data collections get bigger, we must determine how technical variability affects our ability to detect desired patterns when many experiments are combined.

objectiveWe sought to determine the extent to which an underlying signal was masked by technical variability by simulating compendia comprising data aggregated across multiple experiments.

methodWe developed a generative multi-layer neural network to simulate compendia of gene expression experiments from large-scale microbial and human datasets. We compared simulated compendia before and after introducing varying numbers of sources of undesired variability.

resultsThe signal from a baseline compendium was obscured when the number of added sources of variability was small. Applying statistical correction methods rescued the underlying signal in these cases. However, as the number of sources of variability increased, it became easier to detect the original signal even without correction. In fact, statistical correction reduced our power to detect the underlying signal.

conclusionWhen combining a modest number of experiments, it is best to correct for experiment-specific noise. However, when many experiments are combined, statistical correction reduces our ability to extract underlying patterns.

Indexed as

Neural Networks, ComputerHumans

Identifiers

PMID33140829
PMCPMC7607552

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.