Evidence map›Paper›PMID 36882691›Full record

ArticleBMC bioinformatics2023

Propensity scores as a novel method to guide sample allocation and minimize batch effects during the design of high throughput experiments.

Patrick M Carry, Tim Vigers, Lauren A Vanderlinden, Carson Keeter, Fran Dong, Teresa Buckner, Elizabeth Litkowski, Ivana Yang, Jill M Norris, Katerina Kechris

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 7 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

10 authors at 2 institutions in 1 country.

Patrick M CarryColorado Program for Musculoskeletal Research, Department of Orthopedics, University of Colorado Anschutz Medical Campus, 12631 E. 17Th Ave, Room 4602, Mail Stop B202, Aurora, CO, 80045, USA. patrick.carry@cuanschutz.edu.
Tim VigersDepartment of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, USA.
Lauren A VanderlindenDepartment of Epidemiology, Colorado School of Public Health, Aurora, CO, USA.
Carson KeeterColorado Program for Musculoskeletal Research, Department of Orthopedics, University of Colorado Anschutz Medical Campus, 12631 E. 17Th Ave, Room 4602, Mail Stop B202, Aurora, CO, 80045, USA.
Fran DongBarbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Teresa BucknerDepartment of Epidemiology, Colorado School of Public Health, Aurora, CO, USA.
Elizabeth LitkowskiDepartment of Epidemiology, Colorado School of Public Health, Aurora, CO, USA.
Ivana YangDepartment of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Jill M Norris *Department of Epidemiology, Colorado School of Public Health, Aurora, CO, USA.
Katerina Kechris *Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, CO, USA.
Colorado School of Public Health · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Islet Autoimmunity Reversion as a Model of T1D ResiliencyR21AI142483 · NIAID · UNIVERSITY OF COLORADO DENVER · PI NORRIS, JILL M · 2019 to 2020
$428k
NIH HHS 5R21AI142483-02
6 · The paper itself

Abstract

backgroundWe developed a novel approach to minimize batch effects when assigning samples to batches. Our algorithm selects a batch allocation, among all possible ways of assigning samples to batches, that minimizes differences in average propensity score between batches. This strategy was compared to randomization and stratified randomization in a case-control study (30 per group) with a covariate (case vs control, represented as β1, set to be null) and two biologically relevant confounding variables (age, represented as β2, and hemoglobin A1c (HbA1c), represented as β3). Gene expression values were obtained from a publicly available dataset of expression data obtained from pancreas islet cells. Batch effects were simulated as twice the median biological variation across the gene expression dataset and were added to the publicly available dataset to simulate a batch effect condition. Bias was calculated as the absolute difference between observed betas under the batch allocation strategies and the true beta (no batch effects). Bias was also evaluated after adjustment for batch effects using ComBat as well as a linear regression model. In order to understand performance of our optimal allocation strategy under the alternative hypothesis, we also evaluated bias at a single gene associated with both age and HbA1c levels in the 'true' dataset (CAPN13 gene).

resultsPre-batch correction, under the null hypothesis (β1), maximum absolute bias and root mean square (RMS) of maximum absolute bias, were minimized using the optimal allocation strategy. Under the alternative hypothesis (β2 and β3 for the CAPN13 gene), maximum absolute bias and RMS of maximum absolute bias were also consistently lower using the optimal allocation strategy. ComBat and the regression batch adjustment methods performed well as the bias estimates moved towards the true values in all conditions under both the null and alternative hypotheses. Although the differences between methods were less pronounced following batch correction, estimates of bias (average and RMS) were consistently lower using the optimal allocation strategy under both the null and alternative hypotheses.

conclusionsOur algorithm provides an extremely flexible and effective method for assigning samples to batches by exploiting knowledge of covariates prior to sample allocation.

Indexed as

AlgorithmsHealth StatusPropensity ScoreCase-Control StudiesGlycated HemoglobinHumansGlycated HemoglobinBatch effect adjustmentBatch effectsComBatPropensity scores

Identifiers

PMID36882691
PMCPMC9990331
OpenAlexW4323360876

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.