Evidence map›Paper›PMID 28344638›Full record

ArticleAlgorithms for molecular biology : AMB2017

The feasibility of genome-scale biological network inference using Graphics Processing Units.

Raghuram Thiagarajan, Amir Alavi, Jagdeep T Podichetty, Jason N Bazil, Daniel A Beard

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2017. 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. Review
  2. Article
  3. How to deal with parameters for whole-cell modelling.Journal of the Royal Society, Interface · 2017
    Review
  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

5 authors.

Raghuram ThiagarajanPratt & Miller Engineering, WK Smith Drive, New Hudson, MI USA.
Amir AlaviDepartment of Molecular and Integrative Physiology, University of Michigan, North Campus Research Complex, Ann Arbor, MI USA.
Jagdeep T PodichettyDepartment of Molecular and Integrative Physiology, University of Michigan, North Campus Research Complex, Ann Arbor, MI USA.
Jason N BazilDepartment of Molecular and Integrative Physiology, University of Michigan, North Campus Research Complex, Ann Arbor, MI USA.
Daniel A BeardDepartment of Molecular and Integrative Physiology, University of Michigan, North Campus Research Complex, Ann Arbor, MI USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systems research spanning fields from biology to finance involves the identification of models to represent the underpinnings of complex systems. Formal approaches for data-driven identification of network interactions include statistical inference-based approaches and methods to identify dynamical systems models that are capable of fitting multivariate data. Availability of large data sets and so-called 'big data' applications in biology present great opportunities as well as major challenges for systems identification/reverse engineering applications. For example, both inverse identification and forward simulations of genome-scale gene regulatory network models pose compute-intensive problems. This issue is addressed here by combining the processing power of Graphics Processing Units (GPUs) and a parallel reverse engineering algorithm for inference of regulatory networks. It is shown that, given an appropriate data set, information on genome-scale networks (systems of 1000 or more state variables) can be inferred using a reverse-engineering algorithm in a matter of days on a small-scale modern GPU cluster.

Indexed as

Genetic regulatory networksGPUNetwork inferenceReverse engineering

Identifiers

PMID28344638
PMCPMC5360040

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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.