Evidence map›Paper›PMID 25504647›Full record

ArticleBioinformatics (Oxford, England)2015

State of the art prediction of HIV-1 protease cleavage sites.

Thorsteinn Rögnvaldsson, Liwen You, Daniel Garwicz

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Bioinformatics (Oxford, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 18% of its field
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

14 citing papers in PubMed, 62 citations in OpenAlex.

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  5. An Approach to Identifying and Quantifying Bias in Biomedical Data.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Thorsteinn RögnvaldssonCAISR, School of Information Science, Computer and Electrical Engineering, Halmstad University, Halmstad, Sweden and Division of Clinical Chemistry and Pharmacology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Liwen YouCAISR, School of Information Science, Computer and Electrical Engineering, Halmstad University, Halmstad, Sweden and Division of Clinical Chemistry and Pharmacology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Daniel GarwiczCAISR, School of Information Science, Computer and Electrical Engineering, Halmstad University, Halmstad, Sweden and Division of Clinical Chemistry and Pharmacology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Halmstad University · SEUppsala University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationUnderstanding the substrate specificity of human immunodeficiency virus (HIV)-1 protease is important when designing effective HIV-1 protease inhibitors. Furthermore, characterizing and predicting the cleavage profile of HIV-1 protease is essential to generate and test hypotheses of how HIV-1 affects proteins of the human host. Currently available tools for predicting cleavage by HIV-1 protease can be improved.

resultsThe linear support vector machine with orthogonal encoding is shown to be the best predictor for HIV-1 protease cleavage. It is considerably better than current publicly available predictor services. It is also found that schemes using physicochemical properties do not improve over the standard orthogonal encoding scheme. Some issues with the currently available data are discussed. AVAILABILITY AND IMPLEMENTATION: The datasets used, which are the most important part, are available at the UCI Machine Learning Repository. The tools used are all standard and easily available. CONTACT: thorsteinn.rognvaldsson@hh.se.

Indexed as

AlgorithmsArtificial IntelligenceHIV ProteaseHumansOligopeptidesSupport Vector MachineHIV ProteaseOligopeptides

Identifiers

PMID25504647
OpenAlexW2112431023

What OpenQuestion holds

Textmetadata
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.