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Dive into the research topics where Ezequiel L. Nicolazzi is active.

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Featured researches published by Ezequiel L. Nicolazzi.


Animal Genetics | 2012

Molecular tools and analytical approaches for the characterization of farm animal genetic diversity

Johannes A. Lenstra; Linn F. Groeneveld; Herwin Eding; Juha Kantanen; John L. Williams; Pierre Taberlet; Ezequiel L. Nicolazzi; Johann Sölkner; Henner Simianer; E. Ciani; José Fernando Garcia; Michael William Bruford; Paolo Ajmone-Marsan; Steffen Weigend

Genetic studies of livestock populations focus on questions of domestication, within- and among-breed diversity, breed history and adaptive variation. In this review, we describe the use of different molecular markers and methods for data analysis used to address these questions. There is a clear trend towards the use of single nucleotide polymorphisms and whole-genome sequence information, the application of Bayesian or Approximate Bayesian analysis and the use of adaptive next to neutral diversity to support decisions on conservation.


PLOS ONE | 2013

Genome Wide Analysis of Fertility and Production Traits in Italian Holstein Cattle

Giulietta Minozzi; Ezequiel L. Nicolazzi; Alessandra Stella; Stefano Biffani; Riccardo Negrini; Barbara Lazzari; Paolo Ajmone-Marsan; John L. Williams

A genome wide scan was performed on a total of 2093 Italian Holstein proven bulls genotyped with 50K single nucleotide polymorphisms (SNPs), with the objective of identifying loci associated with fertility related traits and to test their effects on milk production traits. The analysis was carried out using estimated breeding values for the aggregate fertility index and for each trait contributing to the index: angularity, calving interval, non-return rate at 56 days, days to first service, and 305 day first parity lactation. In addition, two production traits not included in the aggregate fertility index were analysed: fat yield and protein yield. Analyses were carried out using all SNPs treated separately, further the most significant marker on BTA14 associated to milk quality located in the DGAT1 region was treated as fixed effect. Genome wide association analysis identified 61 significant SNPs and 75 significant marker-trait associations. Eight additional SNP associations were detected when SNP located near DGAT1 was included as a fixed effect. As there were no obvious common SNPs between the traits analyzed independently in this study, a network analysis was carried out to identify unforeseen relationships that may link production and fertility traits.


BMC Genomics | 2014

SNPchiMp: a database to disentangle the SNPchip jungle in bovine livestock

Ezequiel L. Nicolazzi; Matteo Picciolini; Francesco Strozzi; Robert D. Schnabel; Cindy Lawley; Ali Pirani; Fiona Brew; Alessandra Stella

BackgroundCurrently, six commercial whole-genome SNP chips are available for cattle genotyping, produced by two different genotyping platforms. Technical issues need to be addressed to combine data that originates from the different platforms, or different versions of the same array generated by the manufacturer. For example: i) genome coordinates for SNPs may refer to different genome assemblies; ii) reference genome sequences are updated over time changing the positions, or even removing sequences which contain SNPs; iii) not all commercial SNP ID’s are searchable within public databases; iv) SNPs can be coded using different formats and referencing different strands (e.g. A/B or A/C/T/G alleles, referencing forward/reverse, top/bottom or plus/minus strand); v) Due to new information being discovered, higher density chips do not necessarily include all the SNPs present in the lower density chips; and, vi) SNP IDs may not be consistent across chips and platforms. Most researchers and breed associations manage SNP data in real-time and thus require tools to standardise data in a user-friendly manner.DescriptionHere we present SNPchiMp, a MySQL database linked to an open access web-based interface. Features of this interface include, but are not limited to, the following functions: 1) referencing the SNP mapping information to the latest genome assembly, 2) extraction of information contained in dbSNP for SNPs present in all commercially available bovine chips, and 3) identification of SNPs in common between two or more bovine chips (e.g. for SNP imputation from lower to higher density). In addition, SNPchiMp can retrieve this information on subsets of SNPs, accessing such data either via physical position on a supported assembly, or by a list of SNP IDs, rs or ss identifiers.ConclusionsThis tool combines many different sources of information, that otherwise are time consuming to obtain and difficult to integrate. The SNPchiMp not only provides the information in a user-friendly format, but also enables researchers to perform a large number of operations with a few clicks of the mouse. This significantly reduces the time needed to execute the large number of operations required to manage SNP data.


BMC Genomics | 2015

SNPchiMp v.3: integrating and standardizing single nucleotide polymorphism data for livestock species

Ezequiel L. Nicolazzi; Andrea Caprera; Nelson Nazzicari; Paolo Cozzi; Francesco Strozzi; Cindy Lawley; Ali Pirani; Chandrasen Soans; Fiona Brew; Hossein Jorjani; Gary Evans; Barry Simpson; Gwenola Tosser-Klopp; Rudiger Brauning; John L. Williams; Alessandra Stella

BackgroundIn recent years, the use of genomic information in livestock species for genetic improvement, association studies and many other fields has become routine. In order to accommodate different market requirements in terms of genotyping cost, manufacturers of single nucleotide polymorphism (SNP) arrays, private companies and international consortia have developed a large number of arrays with different content and different SNP density. The number of currently available SNP arrays differs among species: ranging from one for goats to more than ten for cattle, and the number of arrays available is increasing rapidly. However, there is limited or no effort to standardize and integrate array- specific (e.g. SNP IDs, allele coding) and species-specific (i.e. past and current assemblies) SNP information.ResultsHere we present SNPchiMp v.3, a solution to these issues for the six major livestock species (cow, pig, horse, sheep, goat and chicken). Original data was collected directly from SNP array producers and specific international genome consortia, and stored in a MySQL database. The database was then linked to an open-access web tool and to public databases. SNPchiMp v.3 ensures fast access to the database (retrieving within/across SNP array data) and the possibility of annotating SNP array data in a user-friendly fashion.ConclusionsThis platform allows easy integration and standardization, and it is aimed at both industry and research. It also enables users to easily link the information available from the array producer with data in public databases, without the need of additional bioinformatics tools or pipelines. In recognition of the open-access use of Ensembl resources, SNPchiMp v.3 was officially credited as an Ensembl E!mpowered tool. Availability at http://bioinformatics.tecnoparco.org/SNPchimp.


Journal of Dairy Science | 2010

Using eigenvalues as variance priors in the prediction of genomic breeding values by principal component analysis

Nicolò Pietro Paolo Macciotta; Giustino Gaspa; Roberto Steri; Ezequiel L. Nicolazzi; Corrado Dimauro; Camillo Pieramati; A. Cappio-Borlino

Genome-wide selection aims to predict genetic merit of individuals by estimating the effect of chromosome segments on phenotypes using dense single nucleotide polymorphism (SNP) marker maps. In the present paper, principal component analysis was used to reduce the number of predictors in the estimation of genomic breeding values for a simulated population. Principal component extraction was carried out either using all markers available or separately for each chromosome. Priors of predictor variance were based on their contribution to the total SNP correlation structure. The principal component approach yielded the same accuracy of predicted genomic breeding values obtained with the regression using SNP genotypes directly, with a reduction in the number of predictors of about 96% and computation time of 99%. Although these accuracies are lower than those currently achieved with Bayesian methods, at least for simulated data, the improved calculation speed together with the possibility of extracting principal components directly on individual chromosomes may represent an interesting option for predicting genomic breeding values in real data with a large number of SNP. The use of phenotypes as dependent variable instead of conventional breeding values resulted in more reliable estimates, thus supporting the current strategies adopted in research programs of genomic selection in livestock.


Frontiers in Genetics | 2015

Prospects and challenges for the conservation of farm animal genomic resources, 2015-2025

Michael William Bruford; Catarina Ginja; Irene Hoffmann; Stéphane Joost; Pablo Orozco-terWengel; Florian J. Alberto; Andreia Amaral; Mario Barbato; Filippo Biscarini; Licia Colli; Mafalda Costa; Ino Curik; Solange Duruz; Maja Ferenčaković; Daniel Fischer; Robert Fitak; Linn F. Groeneveld; Stephen J. G. Hall; Olivier Hanotte; Faiz-ul Hassan; Philippe Helsen; Laura Iacolina; Juha Kantanen; Kevin Leempoel; Johannes A. Lenstra; Paolo Ajmone-Marsan; Charles Masembe; Hendrik-Jan Megens; Mara Miele; Markus Neuditschko

Livestock conservation practice is changing rapidly in light of policy developments, climate change and diversifying market demands. The last decade has seen a step change in technology and analytical approaches available to define, manage and conserve Farm Animal Genomic Resources (FAnGR). However, these rapid changes pose challenges for FAnGR conservation in terms of technological continuity, analytical capacity and integrative methodologies needed to fully exploit new, multidimensional data. The final conference of the ESF Genomic Resources program aimed to address these interdisciplinary problems in an attempt to contribute to the agenda for research and policy development directions during the coming decade. By 2020, according to the Convention on Biodiversitys Aichi Target 13, signatories should ensure that “…the genetic diversity of …farmed and domesticated animals and of wild relatives …is maintained, and strategies have been developed and implemented for minimizing genetic erosion and safeguarding their genetic diversity.” However, the real extent of genetic erosion is very difficult to measure using current data. Therefore, this challenging target demands better coverage, understanding and utilization of genomic and environmental data, the development of optimized ways to integrate these data with social and other sciences and policy analysis to enable more flexible, evidence-based models to underpin FAnGR conservation. At the conference, we attempted to identify the most important problems for effective livestock genomic resource conservation during the next decade. Twenty priority questions were identified that could be broadly categorized into challenges related to methodology, analytical approaches, data management and conservation. It should be acknowledged here that while the focus of our meeting was predominantly around genetics, genomics and animal science, many of the practical challenges facing conservation of genomic resources are societal in origin and are predicated on the value (e.g., socio-economic and cultural) of these resources to farmers, rural communities and society as a whole. The overall conclusion is that despite the fact that the livestock sector has been relatively well-organized in the application of genetic methodologies to date, there is still a large gap between the current state-of-the-art in the use of tools to characterize genomic resources and its application to many non-commercial and local breeds, hampering the consistent utilization of genetic and genomic data as indicators of genetic erosion and diversity. The livestock genomic sector therefore needs to make a concerted effort in the coming decade to enable to the democratization of the powerful tools that are now at its disposal, and to ensure that they are applied in the context of breed conservation as well as development.


Journal of Dairy Science | 2013

Short communication: imputing genotypes using PedImpute fast algorithm combining pedigree and population information.

Ezequiel L. Nicolazzi; S. Biffani; G. Jansen

Routine genomic evaluations frequently include a preliminary imputation step, requiring high accuracy and reduced computing time. A new algorithm, PedImpute (http://dekoppel.eu/pedimpute/), was developed and compared with findhap (http://aipl.arsusda.gov/software/findhap/) and BEAGLE (http://faculty.washington.edu/browning/beagle/beagle.html), using 19,904 Holstein genotypes from a 4-country international collaboration (United States, Canada, UK, and Italy). Different scenarios were evaluated on a sample subset that included only single nucleotide polymorphism from the Bovine low-density (LD) Illumina BeadChip (Illumina Inc., San Diego, CA). Comparative criteria were computing time, percentage of missing alleles, percentage of wrongly imputed alleles, and the allelic squared correlation. Imputation accuracy on ungenotyped animals was also analyzed. The algorithm PedImpute was slightly more accurate and faster than findhap and BEAGLE when sire, dam, and maternal grandsire were genotyped at high density. On the other hand, BEAGLE performed better than both PedImpute and findhap for animals with at least one close relative not genotyped or genotyped at low density. However, computing time and resources using BEAGLE were incompatible with routine genomic evaluations in Italy. Error rate and allelic squared correlation attained by PedImpute ranged from 0.2 to 1.1% and from 96.6 to 99.3%, respectively. When complete genomic information on sire, dam, and maternal grandsire are available, as expected to be the case in the close future in (at least) dairy cattle, and considering accuracies obtained and computation time required, PedImpute represents a valuable choice in routine evaluations among the algorithms tested.


Frontiers in Genetics | 2015

Challenges and opportunities in genetic improvement of local livestock breeds

Filippo Biscarini; Ezequiel L. Nicolazzi; Alessandra Stella; Paul J. Boettcher; G. Gandini

Sufficient genetic variation in livestock populations is necessary both for adaptation to future changes in climate and consumer demand, and for continual genetic improvement of economically important traits. Unfortunately, the current trend is for reduced genetic variation, both within and across breeds. The latter occurs primarily through the loss of small, local breeds. Inferior production is a key driver for loss of small breeds, as they are replaced by high-output international transboundary breeds. Selection to improve productivity of small local breeds is therefore critical for their long term survival. The objective of this paper is to review the technology options available for the genetic improvement of small local breeds and discuss their feasibility. Most technologies have been developed for the high-input breeds and consequently are more favorably applied in that context. Nevertheless, their application in local breeds is not precluded and can yield significant benefits, especially when multiple technologies are applied in close collaboration with farmers and breeders. Breeding strategies that require cooperation and centralized decision-making, such as optimal contribution selection, may in fact be more easily implemented in small breeds.


Journal of Dairy Science | 2012

Prediction of genomic breeding values for dairy traits in Italian Brown and Simmental bulls using a principal component approach.

Maria Annunziata Pintus; Giustino Gaspa; Ezequiel L. Nicolazzi; Daniele Vicario; Attilio Rossoni; Paolo Ajmone-Marsan; A. Nardone; Corrado Dimauro; Nicolò Pietro Paolo Macciotta

The large number of markers available compared with phenotypes represents one of the main issues in genomic selection. In this work, principal component analysis was used to reduce the number of predictors for calculating genomic breeding values (GEBV). Bulls of 2 cattle breeds farmed in Italy (634 Brown and 469 Simmental) were genotyped with the 54K Illumina beadchip (Illumina Inc., San Diego, CA). After data editing, 37,254 and 40,179 single nucleotide polymorphisms (SNP) were retained for Brown and Simmental, respectively. Principal component analysis carried out on the SNP genotype matrix extracted 2,257 and 3,596 new variables in the 2 breeds, respectively. Bulls were sorted by birth year to create reference and prediction populations. The effect of principal components on deregressed proofs in reference animals was estimated with a BLUP model. Results were compared with those obtained by using SNP genotypes as predictors with either the BLUP or Bayes_A method. Traits considered were milk, fat, and protein yields, fat and protein percentages, and somatic cell score. The GEBV were obtained for prediction population by blending direct genomic prediction and pedigree indexes. No substantial differences were observed in squared correlations between GEBV and EBV in prediction animals between the 3 methods in the 2 breeds. The principal component analysis method allowed for a reduction of about 90% in the number of independent variables when predicting direct genomic values, with a substantial decrease in calculation time and without loss of accuracy.


Frontiers in Genetics | 2015

Revisiting demographic processes in cattle with genome-wide population genetic analysis

Pablo Orozco-terWengel; Mario Barbato; Ezequiel L. Nicolazzi; Filippo Biscarini; Marco Milanesi; Wyn Davies; Don Williams; Alessandra Stella; Paolo Ajmone-Marsan; Michael William Bruford

The domestication of the aurochs took place approximately 10,000 years ago giving rise to the two main types of domestic cattle known today, taurine (Bos taurus) domesticated somewhere on or near the Fertile Crescent, and indicine (Bos indicus) domesticated in the Indus Valley. However, although cattle have historically played a prominent role in human society the exact origin of many extant breeds is not well known. Here we used a combination of medium and high-density Illumina Bovine SNP arrays (i.e., ~54,000 and ~770,000 SNPs, respectively), genotyped for over 1300 animals representing 56 cattle breeds, to describe the relationships among major European cattle breeds and detect patterns of admixture among them. Our results suggest modern cross-breeding and ancient hybridisation events have both played an important role, including with animals of indicine origin. We use these data to identify signatures of selection reflecting both domestication (hypothesized to produce a common signature across breeds) and local adaptation (predicted to exhibit a signature of selection unique to a single breed or group of related breeds with a common history) to uncover additional demographic complexity of modern European cattle.

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Paolo Ajmone-Marsan

Catholic University of the Sacred Heart

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Licia Colli

Catholic University of the Sacred Heart

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Riccardo Negrini

Catholic University of the Sacred Heart

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Marco Milanesi

Catholic University of the Sacred Heart

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