Evidence map›Paper›PMID 30104743›Full record

ArticleScientific reports2018

PMLPR: A novel method for predicting subcellular localization based on recommender systems.

Elnaz Mirzaei Mehrabad, Reza Hassanzadeh, Changiz Eslahchi

Open access · goldAbstract read
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Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Elnaz Mirzaei MehrabadDepartment of Computer Science, Faculty of Mathematical Sciences, Shahid Beheshti University, Tehran, Iran.
Reza HassanzadehDepartment of Engineering Sciences, Faculty of Advanced Technologies, University of Mohaghegh Ardabili, Namin, Iran.
Changiz EslahchiDepartment of Computer Science, Faculty of Mathematical Sciences, Shahid Beheshti University, Tehran, Iran. ch-eslahchi@sbu.ac.ir.
Shahid Beheshti University · IRSabalan University of Advanced Technologies · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The importance of protein subcellular localization problem is due to the importance of protein's functions in different cell parts. Moreover, prediction of subcellular locations helps to identify the potential molecular targets for drugs and has an important role in genome annotation. Most of the existing prediction methods assign only one location for each protein. But, since some proteins move between different subcellular locations, they can have multiple locations. In recent years, some multiple location predictors have been introduced. However, their performances are not accurate enough and there is much room for improvement. In this paper, we introduced a method, PMLPR, to predict locations for a protein. PMLPR predicts a list of locations for each protein based on recommender systems and it can properly overcome the multiple location prediction problem. For evaluating the performance of PMLPR, we considered six datasets RAT, FLY, HUMAN, Du et al., DBMLoc and Höglund. The performance of this algorithm is compared with six state-of-the-art algorithms, YLoc, WOLF-PSORT, prediction channel, MDLoc, Du et al. and MultiLoc2-HighRes. The results indicate that our proposed method is significantly superior on RAT and Fly proteins, and decent on HUMAN proteins. Moreover, on the datasets introduced by Du et al., DBMLoc and Höglund, PMLPR has comparable results. For the case study, we applied the algorithms on 8 proteins which are important in cancer research. The results of comparison with other methods indicate the efficiency of PMLPR.

Indexed as

Models, BiologicalAlgorithmsAnimalsComputational BiologyDatabases, ProteinDatasets as TopicDrosophila melanogasterHumansProteinsProtein TransportRatsProteins

Identifiers

PMID30104743
PMCPMC6089892
OpenAlexW2886594612

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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.