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Ewelina Weglarz-Tomczak

dblp:258/1321 · DBLP profile ↗
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1ranked-venue papers
1as first author
1since 2021 · last 2021
0000-0001-8080-2801ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 3 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › systems biology › metabolic network reconstruction
genome-scale metabolic reconstruction
0.512021
M2R: a Python add-on to cobrapy for modifying human genome-scale metabolic reconstruction using the gut microbiota models · Bioinform. 2021
Bioinformatics and computational biology › systems biology
metabolic modeling
0.512021
M2R: a Python add-on to cobrapy for modifying human genome-scale metabolic reconstruction using the gut microbiota models · Bioinform. 2021
Bioinformatics and computational biology › computational microbiology
microbiome analysis
0.112021
M2R: a Python add-on to cobrapy for modifying human genome-scale metabolic reconstruction using the gut microbiota models · Bioinform. 2021
YearPublicationVenuePosition
2021 M2R: a Python add-on to cobrapy for modifying human genome-scale metabolic reconstruction using the gut microbiota models
abstract
MOTIVATION: The gut microbiota is the human body's largest population of microorganisms that interact with human intestinal cells. They use ingested nutrients for fundamental biological processes and have important impacts on human physiology, immunity and metabolome in the gastrointestinal tract. RESULTS: Here, we present M2R, a Python add-on to cobrapy that allows incorporating information about the gut microbiota metabolism models to human genome-scale metabolic models (GEMs) like RECON3D. The idea behind the software is to modify the lower bounds of the exchange reactions in the model using aggregated in- and out-fluxes from selected microbes. M2R enables users to quickly and easily modify the pool of the metabolites that enter and leave the GEM, which is particularly important for those looking into an analysis of the metabolic interaction between the gut microbiota and human cells and its dysregulation. AVAILABILITY AND IMPLEMENTATION: M2R is freely available under an MIT License at https://github.com/e-weglarz-tomczak/m2r. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Ewelina Weglarz-Tomczak, Jakub M. Tomczak, Stanley Brul
Bioinform.1