Evidence map›Paper›PMID 32456608›Full record

ArticleBMC bioinformatics2020

Discovery of significant porcine SNPs for swine breed identification by a hybrid of information gain, genetic algorithm, and frequency feature selection technique.

Kitsuchart Pasupa, Wanthanee Rathasamuth, Sissades Tongsima

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2020. 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
1.2field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

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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

3 authors at 2 institutions in 1 country.

Kitsuchart PasupaFaculty of Information Technology, King Mongkut's Institute of Technology Ladkrabang, Bangkok, 10520, Thailand. kitsuchart@it.kmitl.ac.th.
Wanthanee RathasamuthFaculty of Information Technology, King Mongkut's Institute of Technology Ladkrabang, Bangkok, 10520, Thailand.
Sissades TongsimaNational Biobank of Thailand, National Science and Technology Development Agency, Khong Luang, 12120, Thailand.
King Mongkut's Institute of Technology Ladkrabang · THNational Science and Technology Development Agency · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe number of porcine Single Nucleotide Polymorphisms (SNPs) used in genetic association studies is very large, suitable for statistical testing. However, in breed classification problem, one needs to have a much smaller porcine-classifying SNPs (PCSNPs) set that could accurately classify pigs into different breeds. This study attempted to find such PCSNPs by using several combinations of feature selection and classification methods. We experimented with different combinations of feature selection methods including information gain, conventional as well as modified genetic algorithms, and our developed frequency feature selection method in combination with a common classification method, Support Vector Machine, to evaluate the method's performance. Experiments were conducted on a comprehensive data set containing SNPs from native pigs from America, Europe, Africa, and Asia including Chinese breeds, Vietnamese breeds, and hybrid breeds from Thailand.

resultsThe best combination of feature selection methods-information gain, modified genetic algorithm, and frequency feature selection hybrid-was able to reduce the number of possible PCSNPs to only 1.62% (164 PCSNPs) of the total number of SNPs (10,210 SNPs) while maintaining a high classification accuracy (95.12%). Moreover, the near-identical performance of this PCSNPs set to those of bigger data sets as well as even the entire data set. Moreover, most PCSNPs were well-matched to a set of 94 genes in the PANTHER pathway, conforming to a suggestion by the Porcine Genomic Sequencing Initiative.

conclusionsThe best hybrid method truly provided a sufficiently small number of porcine SNPs that accurately classified swine breeds.

Indexed as

BreedingPolymorphism, Single NucleotideAfricaAlgorithmsAnimalsAsiaEuropeSupport Vector MachineSwineUnited StatesFeature selectionGenetic algorithmInformation gainSingle nucleotide polymorphismsSupport vector machine

Identifiers

PMID32456608
PMCPMC7251909
OpenAlexW3030011650

What OpenQuestion holds

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LicenceCC BY
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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.