Evidence map›Paper›PMID 32628677›Full record

ArticlePloS one2020

A Geometric Clustering Tool (AGCT) to robustly unravel the inner cluster structures of time-series gene expressions.

Richard Nock, Natalia Polouliakh, Frank Nielsen, Keigo Oka, Carlin R Connell, Cedric Heimhofer, Kazuhiro Shibanai, Samik Ghosh, Ken-Ichi Aisaki, Satoshi Kitajima and 3 more

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

13 authors.

Richard NockNICTA/Data61 & the Australian National University, Alexandria, Australia.
Natalia PolouliakhSony Computer Science Laboratories Inc., Tokyo, Japan.ORCID 0000-0001-8266-2697
Frank NielsenSony Computer Science Laboratories Inc., Tokyo, Japan.
Keigo OkaThe University of Tokyo, Tokyo, Japan.
Carlin R ConnellDepartment of Computer Science, Queensland University of Technology, Brisbane, Australia.
Cedric HeimhoferDepartment of Computer Science, ETH Zurich, Zurich, Switzerland.
Kazuhiro ShibanaiDepartment of Computer Science, School of Computing, Tokyo Institute of Technology, Tokyo, Japan.
Samik GhoshSystems Biology Institute, Tokyo, Japan.
Ken-Ichi AisakiNational Institute of Health Science, Kawasaki, Japan.
Satoshi KitajimaNational Institute of Health Science, Kawasaki, Japan.
Jun KannoJapan Bioassay Research Center, Japan Organization of Occupational Health and Safety, Hadano, Japan.
Taketo AkamaSony Computer Science Laboratories Inc., Tokyo, Japan.
Hiroaki KitanoSony Computer Science Laboratories Inc., Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systems biology aims at holistically understanding the complexity of biological systems. In particular, nowadays with the broad availability of gene expression measurements, systems biology challenges the deciphering of the genetic cell machinery from them. In order to help researchers, reverse engineer the genetic cell machinery from these noisy datasets, interactive exploratory clustering methods, pipelines and gene clustering tools have to be specifically developed. Prior methods/tools for time series data, however, do not have the following four major ingredients in analytic and methodological view point: (i) principled time-series feature extraction methods, (ii) variety of manifold learning methods for capturing high-level view of the dataset, (iii) high-end automatic structure extraction, and (iv) friendliness to the biological user community. With a view to meet the requirements, we present AGCT (A Geometric Clustering Tool), a software package used to unravel the complex architecture of large-scale, non-necessarily synchronized time-series gene expression data. AGCT capture signals on exhaustive wavelet expansions of the data, which are then embedded on a low-dimensional non-linear map using manifold learning algorithms, where geometric proximity captures potential interactions. Post-processing techniques, including hard and soft information geometric clustering algorithms, facilitate the summarizing of the complete map as a smaller number of principal factors which can then be formally identified using embedded statistical inference techniques. Three-dimension interactive visualization and scenario recording over the processing helps to reproduce data analysis results without additional time. Analysis of the whole-cell Yeast Metabolic Cycle (YMC) moreover, Yeast Cell Cycle (YCC) datasets demonstrate AGCT's ability to accurately dissect all stages of metabolism and the cell cycle progression, independently of the time course and the number of patterns related to the signal. Analysis of Pentachlorophenol iduced dataset demonstrat how AGCT dissects data to identify two networks: Interferon signaling and NRF2-signaling networks.

Indexed as

Gene ExpressionSoftwareWavelet AnalysisAlgorithmsAnimalsCell CycleComputational BiologyDatasets as TopicGene Expression RegulationLiverMarkov ChainsMicePentachlorophenolRandom AllocationSaccharomyces cerevisiaeSystems BiologyPentachlorophenol

Identifiers

PMID32628677
PMCPMC7337352

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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.