Evidence map›Paper›PMID 27809787›Full record

ArticleBMC genomics2016

Use of SNP genotypes to identify carriers of harmful recessive mutations in cattle populations.

Filippo Biscarini, Hermann Schwarzenbacher, Hubert Pausch, Ezequiel L Nicolazzi, Yuri Pirola, Stefano Biffani

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. 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
1.8field-weighted citation impact, top 13% 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.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 16 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

6 authors at 3 institutions in 2 countries.

Filippo BiscariniDepartment of Bioinformatics and Biostatistics, PTP Science Park, Via Einstein - Loc. Cascina Codazza, Lodi, 26900, Italy. filippo.biscarini@ptp.it.
Hermann SchwarzenbacherZuchtData, Dresdner Straße 89/19, Wien, A-1200, Austria.
Hubert PauschTechnische Universität München, Liesel-Beckmann-Straße 1, Freising-Weihenstephan, D-85354, Germany.
Ezequiel L NicolazziDepartment of Bioinformatics and Biostatistics, PTP Science Park, Via Einstein - Loc. Cascina Codazza, Lodi, 26900, Italy.
Yuri PirolaDISCo, Università degli Studi di Milano-Bicocca, Viale Sarca 336, Milano, Italy.
Stefano BiffaniDepartment of Bioinformatics and Biostatistics, PTP Science Park, Via Einstein - Loc. Cascina Codazza, Lodi, 26900, Italy.
Parco Tecnologico Padano · ITTechnical University of Munich · DEUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSNP (single nucleotide polymorphisms) genotype data are increasingly available in cattle populations and, among other things, can be used to predict carriers of specific mutations. It is therefore convenient to have a practical statistical method for the accurate classification of individuals into carriers and non-carriers. In this paper, we compared - through cross-validation- five classification models (Lasso-penalized logistic regression -Lasso, Support Vector Machines with either linear or radial kernel -SVML and SVMR, k-nearest neighbors -KNN, and multi-allelic gene prediction -MAG), for the identification of carriers of the TUBD1 recessive mutation on BTA19 (Bos taurus autosome 19), known to be associated with high calf mortality. A population of 3116 Fleckvieh and 392 Brown Swiss animals genotyped with the 54K SNP-chip was available for the analysis.

resultsIn general, the use of SNP genotypes proved to be very effective for the identification of mutation carriers. The best predictive models were Lasso, SVML and MAG, with an average error rate, respectively, of 0.2 %, 0.4 % and 0.6 % in Fleckvieh, and 1.2 %, 0.9 % and 1.7 % in Brown Swiss. For the three models, the false positive rate was, respectively, 0.1 %, 0.1 % and 0.2 % in Fleckvieh, and 3.0 %, 2.4 % and 1.6 % in Brown Swiss; the false negative rate was 4.4 %, 7.6 %1.0 % in Fleckvieh, and 0.0 %, 0.1% and 0.8 % in Brown Swiss. MAG appeared to be more robust to sample size reduction: with 25 % of the data, the average error rate was 0.7 % and 2.2 % in Fleckvieh and Brown Swiss, compared to 2.1 % and 5.5 % with Lasso, and 2.6 % and 12.0 % with SVML.

conclusionsThe use of SNP genotypes is a very effective and efficient technique for the identification of mutation carriers in cattle populations. Very few misclassifications were observed, overall and both in the carriers and non-carriers classes. This indicates that this is a very reliable approach for potential applications in cattle breeding.

Indexed as

Genes, RecessiveGenotypeHeterozygoteMutationPolymorphism, Single NucleotideAlgorithmsAnimalsCattleFemaleGenetic Carrier ScreeningMaleReproducibility of ResultsSupport Vector MachineCarrier identificationCattleHaplotypesKNNLasso-penalised logistic regressionMAGRecessive mutationsSNP genotypessupport vector machines

Identifiers

PMID27809787
PMCPMC5093950
OpenAlexW2546594703

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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.