Evidence map›Paper›PMID 35178743›Full record

ArticleStatistics in medicine2022

Assessing reproducibility of high-throughput experiments in the case of missing data.

Roopali Singh, Feipeng Zhang, Qunhua Li

Abstract read
In one paragraph

Article in Statistics in medicine, 2022. 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
–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

5 citing papers in PubMed.

  1. ER-Localized DeadenylaseExploration (Beijing, China) · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. AP2XII-1 and AP2XI-2 Suppress Schizogony Gene Expression inInternational journal of molecular sciences · 2024
    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

3 authors.

Roopali SinghDepartment of Statistics, Pennsylvania State University, University Park, Pennsylvania, USA.ORCID 0000-0001-6539-6622
Feipeng ZhangSchool of Economics and Finance, Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-8110-5837
Qunhua LiDepartment of Statistics, Pennsylvania State University, University Park, Pennsylvania, USA.ORCID 0000-0003-0675-7648

Funding

VISION: ValIdated Systematic IntegratiON of epigenomic dataR24DK106766 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI BLOBEL, GERD A, BODINE, DAVID M. · 2016 to 2020
$6.2M
Statistical methods for improving reproducibility and utility of sequencing dataR01GM109453 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI LI, QUNHUA · 2013 to 2022
$2.3M
Methods to maximize the utility of common fund functional genomic data in multi-ethnic genetic studiesR03OD032630 · OD · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI LIU, DAJIANG · 2021 to 2021
$335k
NIDDK NIH HHS R24 DK106766NIGMS NIH HHS R01 GM109453NIH HHS R01GM109453NIH HHS R03 OD032630
6 · The paper itself

Abstract

High-throughput experiments are an essential part of modern biological and biomedical research. The outcomes of high-throughput biological experiments often have a lot of missing observations due to signals below detection levels. For example, most single-cell RNA-seq (scRNA-seq) protocols experience high levels of dropout due to the small amount of starting material, leading to a majority of reported expression levels being zero. Though missing data contain information about reproducibility, they are often excluded in the reproducibility assessment, potentially generating misleading assessments. In this article, we develop a regression model to assess how the reproducibility of high-throughput experiments is affected by the choices of operational factors (eg, platform or sequencing depth) when a large number of measurements are missing. Using a latent variable approach, we extend correspondence curve regression, a recently proposed method for assessing the effects of operational factors to reproducibility, to incorporate missing values. Using simulations, we show that our method is more accurate in detecting differences in reproducibility than existing measures of reproducibility. We illustrate the usefulness of our method using a single-cell RNA-seq dataset collected on HCT116 cells. We compare the reproducibility of different library preparation platforms and study the effect of sequencing depth on reproducibility, thereby determining the cost-effective sequencing depth that is required to achieve sufficient reproducibility.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisHigh-Throughput Nucleotide SequencingHumansReproducibility of ResultsSequence Analysis, RNAcorrespondence curvehigh throughput experimentsmissing datareproducibilitysequencing depthsingle cell RNA-seq

Identifiers

PMID35178743
PMCPMC9039958

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Registered trials

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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.