Evidence map›Paper›PMID 27379044›Full record

ArticleFrontiers in microbiology2016

From DNA to FBA: How to Build Your Own Genome-Scale Metabolic Model.

Daniel A Cuevas, Janaka Edirisinghe, Chris S Henry, Ross Overbeek, Taylor G O'Connell, Robert A Edwards

Abstract read
In one paragraph

Article in Frontiers in microbiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
–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

25 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  9. Review
  10. Age of Antibiotic Resistance in MDR/XDR Clinical Pathogen ofPharmaceuticals (Basel, Switzerland) · 2023
    Review
  11. Article
  12. Enzyme-constrained metabolic model andComputational and structural biotechnology journal · 2023
    Article
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  15. Article
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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

6 authors.

Daniel A CuevasComputational Science Research Center, San Diego State University, San Diego CA, USA.
Janaka EdirisingheMathematics and Computer Science Division, Argonne National Laboratory, Argonne IL, USA.
Chris S HenryMathematics and Computer Science Division, Argonne National Laboratory, Argonne IL, USA.
Ross OverbeekFellowship for Interpretation of Genomes, Burr Ridge IL, USA.
Taylor G O'ConnellBiological and Medical Informatics Research Center, San Diego State University, San Diego CA, USA.
Robert A EdwardsComputational Science Research Center, San Diego State University, San DiegoCA, USA; Biological and Medical Informatics Research Center, San Diego State University, San DiegoCA, USA; Department of Computer Science, San Diego State University, San DiegoCA, USA; Department of Biology, San Diego State University, San DiegoCA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbiological studies are increasingly relying on in silico methods to perform exploration and rapid analysis of genomic data, and functional genomics studies are supplemented by the new perspectives that genome-scale metabolic models offer. A mathematical model consisting of a microbe's entire metabolic map can be rapidly determined from whole-genome sequencing and annotating the genomic material encoded in its DNA. Flux-balance analysis (FBA), a linear programming technique that uses metabolic models to predict the phenotypic responses imposed by environmental elements and factors, is the leading method to simulate and manipulate cellular growth in silico. However, the process of creating an accurate model to use in FBA consists of a series of steps involving a multitude of connections between bioinformatics databases, enzyme resources, and metabolic pathways. We present the methodology and procedure to obtain a metabolic model using PyFBA, an extensible Python-based open-source software package aimed to provide a platform where functional annotations are used to build metabolic models (http://linsalrob.github.io/PyFBA). Backed by the Model SEED biochemistry database, PyFBA contains methods to reconstruct a microbe's metabolic map, run FBA upon different media conditions, and gap-fill its metabolism. The extensibility of PyFBA facilitates novel techniques in creating accurate genome-scale metabolic models.

Indexed as

flux-balance analysisgenome annotationin silico modelingmetabolic modelingmetabolic reconstructionmodel SEED

Identifiers

PMID27379044
PMCPMC4911401

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.