Evidence map›Paper›PMID 38233793›Full record

ArticleBMC bioinformatics2024

Temporal classification of short time series data.

Benedikt Venn, Thomas Leifeld, Ping Zhang, Timo Mühlhaus

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Benedikt VennComputational Systems Biology, RPTU Kaiserslautern, 67663, Kaiserslautern, Germany.
Thomas LeifeldInstitute of Automatic Control, RPTU Kaiserslautern, 67663, Kaiserslautern, Germany.
Ping ZhangInstitute of Automatic Control, RPTU Kaiserslautern, 67663, Kaiserslautern, Germany.
Timo MühlhausComputational Systems Biology, RPTU Kaiserslautern, 67663, Kaiserslautern, Germany. timo.muehlhaus@rptu.de.

Funding

Deutsche Forschungsgemeinschaft TR175 270050988 Projekt D02
6 · The paper itself

Abstract

motivationWithin the frame of their genetic capacity, organisms are able to modify their molecular state to cope with changing environmental conditions or induced genetic disposition. As high throughput methods are becoming increasingly affordable, time series analysis techniques are applied frequently to study the complex dynamic interplay between genes, proteins, and metabolites at the physiological and molecular level. Common analysis approaches fail to simultaneously include (i) information about the replicate variance and (ii) the limited number of responses/shapes that a biological system is typically able to take.

resultsWe present a novel approach to model and classify short time series signals, conceptually based on a classical time series analysis, where the dependency of the consecutive time points is exploited. Constrained spline regression with automated model selection separates between noise and signal under the assumption that highly frequent changes are less likely to occur, simultaneously preserving information about the detected variance. This enables a more precise representation of the measured information and improves temporal classification in order to identify biologically interpretable correlations among the data. AVAILABILITY AND IMPLEMENTATION: An open source F# implementation of the presented method and documentation of its usage is freely available in the TempClass repository, https://github.com/CSBiology/TempClass  [58].

Indexed as

Research DesignTime FactorsOmics analyisProfile classificationSmoothing splineTime series analysis

Identifiers

PMID38233793
PMCPMC10792935

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.