Evidence map›Paper›PMID 30225593›Full record

ArticleBulletin of mathematical biology2019

Data-Driven Method for Efficient Characterization of Rare Event Probabilities in Biochemical Systems.

Min K Roh

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2019. 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

1 author.

Min K RohInstitute for Disease Modeling, 3150 139th Ave SE, Bellevue, WA, 98005, USA. mroh@idmod.org.ORCID 0000-0003-1976-1929

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As mathematical models and computational tools become more sophisticated and powerful to accurately depict system dynamics, numerical methods that were previously considered computationally impractical started being utilized for large-scale simulations. Methods that characterize a rare event in biochemical systems are part of such phenomenon, as many of them are computationally expensive and require high-performance computing. In this paper, we introduce an enhanced version of the doubly weighted stochastic simulation algorithm (dwSSA) (Daigle et al. in J Chem Phys 134:044110, 2011), called dwSSA[Formula: see text], that significantly improves the speed of convergence to the rare event of interest when the conventional multilevel cross-entropy method in dwSSA is either unable to converge or converges very slowly. This achievement is enabled by a novel polynomial leaping method that uses past data to detect slow convergence and attempts to push the system toward the rare event. We demonstrate the performance of dwSSA[Formula: see text] on two systems-a susceptible-infectious-recovered-susceptible disease dynamics model and a yeast polarization model-and compare its computational efficiency to that of dwSSA.

Indexed as

AlgorithmsModels, BiologicalBiochemical PhenomenaCell CycleCommunicable DiseasesComputer SimulationDecision TreesHumansKineticsMathematical ConceptsProbabilitySaccharomyces cerevisiaeStochastic ProcessesdwSSAGillespie algorithmImportance samplingRare event probability estimationSSAStochastic simulation

Identifiers

PMID30225593
PMCPMC6677716

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.