Evidence map›Paper›PMID 31512748›Full record

ArticleAnimal genetics2019

Targeted genotyping by sequencing: a new way to genome profile the cat.

M Longeri, A Chiodi, M Brilli, A Piazza, L A Lyons, G Sofronidis, M C Cozzi, C Bazzocchi

Abstract read
In one paragraph

Article in Animal genetics, 2019. 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. Article
  3. Article
  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

8 authors.

M LongeriDepartment of Veterinary Medicine, University of Milan, Milano, 20133, Italy.ORCID https://orcid.org/0000-0001-7863-1855
A ChiodiDepartment of Earth and Environmental Sciences, University of Pavia, Pavia, 27100, Italy.
M BrilliDepartment of Biosciences, University of Milan, Milano, 20133, Italy.
A PiazzaPaediatric Clinical Research Centre "Romeo ed Enrica Invernizzi", University of Milan, Milano, 20157, Italy.
L A LyonsDepartment of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO, 65211, USA.
G SofronidisOrivet Genetic Pet Care, Suite 102/163-169 Inkerman Street, St. Kilda, Vic., 3182, Australia.
M C CozziDepartment of Veterinary Medicine, University of Milan, Milano, 20133, Italy.
C BazzocchiDepartment of Veterinary Medicine, University of Milan, Milano, 20133, Italy.

Funding

University of Milan Linea 2 University of Milan_CBA22_2018AB
6 · The paper itself

Abstract

Targeted GBS is a recent approach for obtaining an effective characterization for hundreds to thousands of markers. The high throughput of next-generation sequencing technologies, moreover, allows sample multiplexing. The aims of this study were to (i) define a panel of single nucleotide polymorphisms (SNPs) in the cat, (ii) use GBS for profiling 16 cats, and (iii) evaluate the performance with respect to the inference using standard approaches at different coverage thresholds, thereby providing useful information for designing similar experiments. Probes for sequencing 230 variants were designed based on the Felis_catus_8.0. 8.0 genome. The regions comprised anonymous and non-anonymous SNPs. Sixteen cat samples were analysed, some of which had already been genotyped in a large group of loci and one having been whole-genome sequenced in the 99_Lives Cat Genome Sequencing Project. The accuracy of the method was assessed by comparing the GBS results with the genotypes already available. Overall, GBS achieved good performance, with 92-96% correct assignments, depending on the coverage threshold used to define the set of trustable genotypes. Analyses confirmed that (i) the reliability of the inference of each genotype depends on the coverage at that locus and (ii) the fraction of target loci whose genotype can be inferred correctly is a function of the total coverage. GBS proves to be a valid alternative to other methods. Data suggested a depth of less than 11× is required for greater than 95% accuracy. However, sequencing depth must be adapted to the total size of the targets to ensure proper genotype inference.

Indexed as

AnimalsCatsGenomeGenotyping TechniquesMicrosatellite RepeatsPolymorphism, Single NucleotideDNA profilingFelis catusgenotyping-by-sequencingsingle nucleotide polymorphisms

Identifiers

PMID31512748
PMCPMC6899796

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.