Evidence map›Paper›PMID 25502381›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2015

GENN: a GEneral Neural Network for learning tabulated data with examples from protein structure prediction.

Eshel Faraggi, Andrzej Kloczkowski

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2015. 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

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

6 citing papers in PubMed.

  1. AlphaFold2, SPINE-X, and Seder on Four Hard CASP Targets.Methods in molecular biology (Clifton, N.J.) · 2025
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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

2 authors.

Eshel FaraggiDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana, 46202, USA, efaraggi@gmail.com.
Andrzej Kloczkowski

Funding

Coarse-Grained Models of ProteinsR01GM072014 · NIGMS · IOWA STATE UNIVERSITY · PI JERNIGAN, ROBERT L · 2004 to 2012
$2.3M
Modeling Ribosomal Control, Function and AssemblyR01GM073095 · NIGMS · IOWA STATE UNIVERSITY · PI JERNIGAN, ROBERT L · 2006 to 2009
$1.0M
NIGMS NIH HHS R01 GM072014NIGMS NIH HHS R01GM072014NIGMS NIH HHS R01 GM073095NIGMS NIH HHS R01GM073095
6 · The paper itself

Abstract

We present a GEneral Neural Network (GENN) for learning trends from existing data and making predictions of unknown information. The main novelty of GENN is in its generality, simplicity of use, and its specific handling of windowed input/output. Its main strength is its efficient handling of the input data, enabling learning from large datasets. GENN is built on a two-layered neural network and has the option to use separate inputs-output pairs or window-based data using data structures to efficiently represent input-output pairs. The program was tested on predicting the accessible surface area of globular proteins, scoring proteins according to similarity to native, predicting protein disorder, and has performed remarkably well. In this paper we describe the program and its use. Specifically, we give as an example the construction of a similarity to native protein scoring function that was constructed using GENN. The source code and Linux executables for GENN are available from Research and Information Systems at http://mamiris.com and from the Battelle Center for Mathematical Medicine at http://mathmed.org. Bugs and problems with the GENN program should be reported to EF.

Indexed as

Neural Networks, ComputerComputational BiologyModels, MolecularProtein ConformationProteinsSoftwareProteins

Identifiers

PMID25502381
PMCPMC6930076

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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.