Evidence map›Paper›PMID 32396573›Full record

ArticlePLoS computational biology2020

StanDep: Capturing transcriptomic variability improves context-specific metabolic models.

Chintan J Joshi, Song-Min Schinn, Anne Richelle, Isaac Shamie, Eyleen J O'Rourke, Nathan E Lewis

Erratum issuedAbstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Chintan J JoshiDepartment of Pediatrics, University of California, San Diego, School of Medicine, La Jolla, CA, United States of America.
Song-Min SchinnDepartment of Pediatrics, University of California, San Diego, School of Medicine, La Jolla, CA, United States of America.ORCID 0000-0002-5727-4016
Anne RichelleDepartment of Pediatrics, University of California, San Diego, School of Medicine, La Jolla, CA, United States of America.
Isaac ShamieNovo Nordisk Foundation Center for Biosustainability at the University of California, San Diego, School of Medicine, La Jolla, CA, United States of America.
Eyleen J O'RourkeDepartment of Biology, University of Virginia, Charlottesville, VA, United States of America.ORCID 0000-0003-0503-4181
Nathan E LewisDepartment of Pediatrics, University of California, San Diego, School of Medicine, La Jolla, CA, United States of America.ORCID 0000-0001-7700-3654

Funding

Unraveling the mammalian secretory pathway through systems biology and algorithm developmentR35GM119850 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LEWIS, NATHAN ENOCH · 2016 to 2025
$4.3M
NIGMS NIH HHS R35 GM119850
6 · The paper itself

Abstract

Diverse algorithms can integrate transcriptomics with genome-scale metabolic models (GEMs) to build context-specific metabolic models. These algorithms require identification of a list of high confidence (core) reactions from transcriptomics, but parameters related to identification of core reactions, such as thresholding of expression profiles, can significantly change model content. Importantly, current thresholding approaches are burdened with setting singular arbitrary thresholds for all genes; thus, resulting in removal of enzymes needed in small amounts and even many housekeeping genes. Here, we describe StanDep, a novel heuristic method for using transcriptomics to identify core reactions prior to building context-specific metabolic models. StanDep clusters gene expression data based on their expression pattern across different contexts and determines thresholds for each cluster using data-dependent statistics, specifically standard deviation and mean. To demonstrate the use of StanDep, we built hundreds of models for the NCI-60 cancer cell lines. These models successfully increased the inclusion of housekeeping reactions, which are often lost in models built using standard thresholding approaches. Further, StanDep also provided a transcriptomic explanation for inclusion of lowly expressed reactions that were otherwise only supported by model extraction methods. Our study also provides novel insights into how cells may deal with context-specific and ubiquitous functions. StanDep, as a MATLAB toolbox, is available at https://github.com/LewisLabUCSD/StanDep.

Indexed as

AlgorithmsComputational BiologyGene Expression ProfilingGenomeHumansMetabolic Networks and PathwaysMetabolomicsModels, BiologicalModels, TheoreticalTranscriptome

Identifiers

PMID32396573
PMCPMC7244210

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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.