Evidence map›Paper›PMID 29104899›Full record

ArticleIEEE life sciences letters2016

Regularization Techniques to Overcome Overparameterization of Complex Biochemical Reaction Networks.

Daniel P Howsmon, Juergen Hahn

Abstract read
In one paragraph

Article in IEEE life sciences letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

2 authors.

Daniel P HowsmonBiomedical Engineering Department at Rensselaer Polytechnic Institute, Troy, NY 12180 USA (hahnj@rpi.edu).
Juergen HahnChemical and Biological Engineering Department at Rensselaer Polytechnic Institute, Troy, NY 12180 USA (howsmd@rpi.edu).

Funding

Modeling and Analysis of the Role of Microbiota Metabolites in T-Cell DifferentiationR01AI110642 · NIAID · TEXAS ENGINEERING EXPERIMENT STATION · PI ALANIZ, ROBERT CHRISTOPHER, HAHN, JUERGEN · 2015 to 2019
$2.0M
NIAID NIH HHS R01 AI110642
6 · The paper itself

Abstract

Models of biochemical reaction networks commonly contain a large number of parameters while at the same time there is only a limited amount of (noisy) data available for their estimation. As such, the values of many parameters are not well known as nominal parameter values have to be determined from the open scientific literature and a significant number of the values may have been derived in different cell types or organisms than that which is modeled. There clearly is a need to estimate at least some of the parameter values from experimental data, however, the small amount of available data and the large number of parameters commonly found in these types of models, require the use of regularization techniques to avoid over fitting. A tutorial of regularization techniques, including parameter set selection, precedes a case study of estimating parameters in a signal transduction network. Cross validation rather than fitting results are presented to further emphasize the need for models that generalize well to new data instead of simply fitting the current data.

Indexed as

computational systems biologynonlinear dynamical systemsparameter estimation

Identifiers

PMID29104899
PMCPMC5665387

What OpenQuestion holds

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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.