Evidence map›Paper›PMID 30866799›Full record

ArticleGenetics, selection, evolution : GSE2019

Machine learning applied to transcriptomic data to identify genes associated with feed efficiency in pigs.

Miriam Piles, Carlos Fernandez-Lozano, María Velasco-Galilea, Olga González-Rodríguez, Juan Pablo Sánchez, David Torrallardona, Maria Ballester, Raquel Quintanilla

Open access · goldAbstract read
In one paragraph

Article in Genetics, selection, evolution : GSE, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 43 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

8 authors at 2 institutions in 1 country.

Miriam PilesAnimal Breeding and Genetics Program, Institute of Agriculture and Food Research and Technology (IRTA), Torre Marimon s/n, 08140, Caldes de Montbui, Barcelona, Spain. miriam.piles@irta.es.ORCID http://orcid.org/0000-0001-8265-9930
Carlos Fernandez-LozanoComputer Science Department, University of A Coruña, Campus Elviña s/n, 15071, A Coruña, Spain.
María Velasco-GalileaAnimal Breeding and Genetics Program, Institute of Agriculture and Food Research and Technology (IRTA), Torre Marimon s/n, 08140, Caldes de Montbui, Barcelona, Spain.
Olga González-RodríguezAnimal Breeding and Genetics Program, Institute of Agriculture and Food Research and Technology (IRTA), Torre Marimon s/n, 08140, Caldes de Montbui, Barcelona, Spain.
Juan Pablo SánchezAnimal Breeding and Genetics Program, Institute of Agriculture and Food Research and Technology (IRTA), Torre Marimon s/n, 08140, Caldes de Montbui, Barcelona, Spain.
David TorrallardonaAnimal Nutrition Program, Institute of Agriculture and Food Research and Technology (IRTA), Mas de Bover, 43120, Constantí, Spain.
Maria BallesterAnimal Breeding and Genetics Program, Institute of Agriculture and Food Research and Technology (IRTA), Torre Marimon s/n, 08140, Caldes de Montbui, Barcelona, Spain.
Raquel QuintanillaAnimal Breeding and Genetics Program, Institute of Agriculture and Food Research and Technology (IRTA), Torre Marimon s/n, 08140, Caldes de Montbui, Barcelona, Spain.
Institute of Agrifood Research and Technology · ESUniversidade da Coruña · ES

Funding

European Union Seventh Framework Programme (FP7/2007-2013) 311794Spanish Ministry of Economy and Competitiveness FJCI-2015-26071
6 · The paper itself

Abstract

backgroundTo date, the molecular mechanisms that underlie residual feed intake (RFI) in pigs are unknown. Results from different genome-wide association studies and gene expression analyses are not always consistent. The aim of this research was to use machine learning to identify genes associated with feed efficiency (FE) using transcriptomic (RNA-Seq) data from pigs that are phenotypically extreme for RFI.

methodsRFI was computed by considering within-sex regression on mean metabolic body weight, average daily gain, and average backfat gain. RNA-Seq analyses were performed on liver and duodenum tissue from 32 high and 33 low RFI pigs collected at 153 d of age. Machine-learning algorithms were used to predict RFI class based on gene expression levels in liver and duodenum after adjusting for batch effects. Genes were ranked according to their contribution to the classification using the permutation accuracy importance score in an unbiased random forest (RF) algorithm based on conditional inference. Support vector machine, RF, elastic net (ENET) and nearest shrunken centroid algorithms were tested using different subsets of the top rank genes. Nested resampling for hyperparameter tuning was implemented with tenfold cross-validation in the outer and inner loops.

resultsThe best classification was obtained with ENET using the expression of 200 genes in liver [area under the receiver operating characteristic curve (AUROC): 0.85; accuracy: 0.78] and 100 genes in duodenum (AUROC: 0.76; accuracy: 0.69). Canonical pathways and candidate genes that were previously reported as associated with FE in several species were identified. The most remarkable pathways and genes identified were NRF2-mediated oxidative stress response and aldosterone signalling in epithelial cells, the DNAJC6, DNAJC1, MAPK8, PRKD3 genes in duodenum, and melatonin degradation II, PPARα/RXRα activation, and GPCR-mediated nutrient sensing in enteroendocrine cells and SMOX, IL4I1, PRKAR2B, CLOCK and CCK genes in liver.

conclusionsML algorithms and RNA-Seq expression data were found to provide good performance for classifying pigs into high or low RFI groups. Classification was better with gene expression data from liver than from duodenum. Genes associated with FE in liver and duodenum tissue that can be used as predictive biomarkers for this trait were identified.

Indexed as

Machine LearningTranscriptomeAnimal FeedAnimal Nutritional Physiological PhenomenaAnimalsBreedingGene Expression ProfilingSwine

Identifiers

PMID30866799
PMCPMC6417084
OpenAlexW2922048844

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.