Evidence map›Paper›PMID 36018232›Full record

ArticleBioinformatics (Oxford, England)2022

FastMix: a versatile data integration pipeline for cell type-specific biomarker inference.

Yun Zhang, Hao Sun, Aishwarya Mandava, Brian D Aevermann, Tobias R Kollmann, Richard H Scheuermann, Xing Qiu, Yu Qian

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Yun ZhangDepartment of Informatics, J. Craig Venter Institute, La Jolla, CA 92037, USA.ORCID 0000-0003-2707-5881
Hao SunDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY 14642, USA.
Aishwarya MandavaDepartment of Informatics, J. Craig Venter Institute, La Jolla, CA 92037, USA.
Brian D AevermannDepartment of Informatics, J. Craig Venter Institute, La Jolla, CA 92037, USA.
Tobias R KollmannSystems Vaccinology, Telethon Kids Institute, Perth Children's Hospital, University of Western Australia, Nedlands, WA 6009, Australia.
Richard H ScheuermannDepartment of Informatics, J. Craig Venter Institute, La Jolla, CA 92037, USA.
Xing QiuDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY 14642, USA.ORCID 0000-0002-2330-3544
Yu QianDepartment of Informatics, J. Craig Venter Institute, La Jolla, CA 92037, USA.

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
Transformative Computational Infrastructures for Cell-Based Biomarker DiagnosticsU01TR001801 · NCATS · J. CRAIG VENTER INSTITUTE, INC. · PI QIAN, YU, SCHEUERMANN, RICHARD H · 2016 to 2020
$4.0M
Reproducible Analytics for Secondary Analyses of ImmPort Vaccination-Related Cytometry DataUH2AI132342 · NIAID · J. CRAIG VENTER INSTITUTE, INC. · PI QIAN, YU · 2018 to 2019
$536k
National Center for Advancing Translational Sciences [NCATS U01TR001801National Institute of Allergy and Infectious Diseases [NIAID UH2AI132342NCATS NIH HHS U01 TR001801NCATS NIH HHS UL1 TR002001NIAID NIH HHS HHSN272201200005CNIAID NIH HHS UH2 AI132342University of Rochester [NCATS CTSA UL1TR002001
6 · The paper itself

Abstract

motivationFlow cytometry (FCM) and transcription profiling are the two widely used assays in translational immunology research. However, there is no data integration pipeline for analyzing these two types of assays together with experiment variables for biomarker inference. Current FCM data analysis mainly relies on subjective manual gating analysis, which is difficult to be directly integrated with other automated computational methods. Existing deconvolutional analysis of bulk transcriptomics relies on predefined marker genes in the transcriptomics data, which are unavailable for novel cell types and does not utilize the FCM data that provide canonical phenotypic definitions of the cell types.

resultsWe developed a novel analytics pipeline-FastMix-for computational immunology, which integrates flow cytometry, bulk transcriptomics and clinical covariates for identifying cell type-specific gene expression signatures and biomarker genes. FastMix addresses the 'large p, small n' problem in the gene expression and flow cytometry integration analysis via a linear mixed effects model (LMER) for both cross-sectional and longitudinal studies. Its novel moment-based estimator not only reduces bias in parameter estimation but also is more efficient than iterative optimization. The FastMix pipeline also includes a cutting-edge flow cytometry data analysis method-DAFi-for identifying cell populations of interest and their characteristics. Simulation studies showed that FastMix produced smaller type I/II errors than competing methods. Validation using real data of two vaccine studies showed that FastMix identified a consistent set of signature genes as in independent single-cell RNA-seq analysis, producing additional interesting findings. AVAILABILITY AND IMPLEMENTATION: Source code of FastMix is publicly available at https://github.com/terrysun0302/FastMix. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

SoftwareTranscriptomeBiomarkersCross-Sectional StudiesData AnalysisBiomarkers

Identifiers

PMID36018232
PMCPMC9801972

What Socratic holds

Textmetadata
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 Socratic graph.