Evidence map›Paper›PMID 30026811›Full record

ArticleBioData mining2018

Feature selection for gene prediction in metagenomic fragments.

Amani Al-Ajlan, Achraf El Allali

Abstract read
In one paragraph

Article in BioData mining, 2018. 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. Article
  2. Bioinformatics advances · 2023
    Article
  3. Machine learning applications in RNA modification sites prediction.Computational and structural biotechnology journal · 2021
    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

2 authors.

Amani Al-AjlanCollege of Computer and Information Sciences, Computer Science Department, King Saud University, Riyadh, Saudi Arabia.ORCID 0000-0002-6807-1425
Achraf El AllaliCollege of Computer and Information Sciences, Computer Science Department, King Saud University, Riyadh, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComputational approaches, specifically machine-learning techniques, play an important role in many metagenomic analysis algorithms, such as gene prediction. Due to the large feature space, current de novo gene prediction algorithms use different combinations of classification algorithms to distinguish between coding and non-coding sequences.

resultsIn this study, we apply a filter method to select relevant features from a large set of known features instead of combining them using linear classifiers or ignoring their individual coding potential. We use minimum redundancy maximum relevance (mRMR) to select the most relevant features. Support vector machines (SVM) are trained using these features, and the classification score is transformed into the posterior probability of the coding class. A greedy algorithm uses the probability of overlapped candidate genes to select the final genes. Instead of using one model for all sequences, we train an ensemble of SVM models on mutually exclusive datasets based on GC content and use the appropriated model to classify candidate genes based on their read's GC content.

conclusionOur proposed algorithm achieves an improvement over some existing algorithms. mRMR produces promising results in gene prediction. It improves classification performance and feature interpretation. Our research serves as a basis for future studies on feature selection for gene prediction.

Indexed as

Feature selectionGene predictionMetagenomicsmRMRORFProkaryotes

Identifiers

PMID30026811
PMCPMC6047368

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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.