Evidence map›Paper›PMID 30594246›Full record

ArticleBMC systems biology2018

Parameter estimation of qualitative biological regulatory networks on high performance computing hardware.

Muhammad Tariq Saeed, Jamil Ahmad, Jan Baumbach, Josch Pauling, Aamir Shafi, Rehan Zafar Paracha, Asad Hayat, Amjad Ali

Abstract read
In one paragraph

Article in BMC systems biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Verifiable biology.Journal of the Royal Society, Interface · 2023
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Joint learning of multiple gene networks from single-cell gene expression data.Computational and structural biotechnology journal · 2020
    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

8 authors.

Muhammad Tariq SaeedResearch Centre for Modeling and Simulation (RCMS), NUST, Islamabad, 44000, Pakistan.
Jamil AhmadResearch Centre for Modeling and Simulation (RCMS), NUST, Islamabad, 44000, Pakistan. dr.ahmad.jamil@gmail.com.
Jan BaumbachChair of Experimental Bioinformatics, TUM School of Life Sciences Weihenstephan, Maximus-von-Imhof-Forum 3, Freising, 85354, Germany.
Josch PaulingComputational Lipidomics group, Chair of Experimental Bioinformatics, TUM School of Life Sciences Weihenstephan, Maximus-von-Imhof-Forum 3, 85354, Freising, Germany.
Aamir ShafiDepartment of Computer Science, National University of Computer and Emerging Sciences, Lahore, Pakistan.
Rehan Zafar ParachaResearch Centre for Modeling and Simulation (RCMS), NUST, Islamabad, 44000, Pakistan.
Asad HayatResearch Centre for Modeling and Simulation (RCMS), NUST, Islamabad, 44000, Pakistan.
Amjad AliAtta-ur-Rahman School of Applied Bio sciences (ASAB), NUST, Islamabad, 44000, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiological Regulatory Networks (BRNs) are responsible for developmental and maintenance related functions in organisms. These functions are implemented by the dynamics of BRNs and are sensitive to regulations enforced by specific activators and inhibitors. The logical modeling formalism by René Thomas incorporates this sensitivity with a set of logical parameters modulated by available regulators, varying with time. With the increase in complexity of BRNs in terms of number of entities and their interactions, the task of parameters estimation becomes computationally expensive with existing sequential SMBioNET tool. We extend the existing sequential implementation of SMBioNET by using a data decomposition approach using a Java messaging library called MPJ Express. The approach divides the parameters space into different regions and each region is then explored in parallel on High Performance Computing (HPC) hardware.

resultsThe performance of the parallel approach is evaluated on BRNs of different sizes, and experimental results on multicore and cluster computers showed almost linear speed-up. This parallel code can be executed on a wide range of concurrent hardware including laptops equipped with multicore processors, and specialized distributed memory computer systems. To demonstrate the application of parallel implementation, we selected a case study of Hexosamine Biosynthetic Pathway (HBP) in cancer progression to identify potential therapeutic targets against cancer. A set of logical parameters were computed for HBP model that directs the biological system to a state of recovery. Furthermore, the parameters also suggest a potential therapeutic intervention that restores homeostasis. Additionally, the performance of parallel application was also evaluated on a network (comprising of 23 entities) of Fibroblast Growth Factor Signalling in Drosophila melanogaster.

conclusionsQualitative modeling framework is widely used for investigating dynamics of biological regulatory networks. However, computation of model parameters in qualitative modeling is computationally intensive. In this work, we presented results of our Java based parallel implementation that provides almost linear speed-up on both multicore and cluster platforms. The parallel implementation is available at https://psmbionet.github.io .

Indexed as

Computing MethodologiesAnimalsComputational BiologyDrosophila melanogasterFibroblast Growth FactorsModels, BiologicalN-AcetylglucosaminyltransferasesNeoplasmsSignal TransductionFibroblast Growth FactorsN-AcetylglucosaminyltransferasesBiological regulatory networksHexosamine biosynthetic pathway (HBP)Model checkingMPJ expressParallel SMBioNetParameter estimationQualitative modelingRené Thomas framework

Identifiers

PMID30594246
PMCPMC6311083

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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.