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dc.contributor.authorANDRADE, A. C.pt_BR
dc.contributor.authorSILVA JUNIOR, O. B. dapt_BR
dc.contributor.authorCARNEIRO, F.pt_BR
dc.contributor.authorMARRACCINI, P.pt_BR
dc.contributor.authorGRATTAPAGLIA, D.pt_BR
dc.date.accessioned2017-03-06T11:11:11Zpt_BR
dc.date.available2017-03-06T11:11:11Zpt_BR
dc.date.created2017-03-06pt_BR
dc.date.issued2017pt_BR
dc.identifier.citationIn: PLANT & ANIMAL GENOME, 25., 2017, San Diego. Final program & exhibite guide... San Diego: USDA, 2017.pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1066344pt_BR
dc.descriptionGenome-wide SNP genotyping platforms aiming at high-throughput and high-precision genotyping constitute an essential tool to advance breeding by genomic prediction and gene discovery by GWAS. Recent advances in coffee genomics with the sequencing of the Coffea canephora reference genome, has provided the coffee scientific community the necessary resource to develop a SNPs toolbox for genome-wide genotyping. C. canephora, an allogamous diploid species, and one of the parents of the allotetraploid C. arabica, has been an important source of genetic variability for breeding programs of both cultivated species. Highly heterozygous genomes such as C. canephora require a much higher sequence depth to reach acceptable marker call rates and genotype accuracy, when using sequence-based genotyping methods such that their cost effectiveness may not be realized. Here we describe the development and validation of a 26K Axiom SNP array (Affymetrix) whose genome- wide distributed SNP content was discovered from pooled whole-genome resequencing of C. canephora accessions covering most of its known genetic diversity. Besides facilitating low cost, high marker density, polymorphism and speed of data generation, the platform displays high genotype call accuracy and reproducibility. Genotyping validation resulted in 24,073 SNPs (94.6%) successfully converted out of the 25,456 SNPs on the array. 20,982 markers(87.1%) were scored as providing high-resolution genotypic data in a set of 800 individuals of a breeding population in which 19,586 (81.4%) were polymorphic and 1,396 (5.8%) were monomorphic. The remaining set of 3,091 (12.8%) successfully converted markers were of lower accuracy in the studied sample and may require additional cluster analysis to proper biological interpretation, i.e. targeting CNVs. This large validated SNP collection provides a powerful tool for molecular breeding and population genetics investigation within coffee species. Some preliminary results of a GWAS using this genotyping platform will be presented.pt_BR
dc.language.isoengeng
dc.rightsopenAccesseng
dc.subjectCoffee canephorapt_BR
dc.subjectCoffee Berry Borerpt_BR
dc.titleTowards GWAS and Genomic Prediction in Coffee: Development and Validation of a 26K SNP Chip for Coffea Canephora.pt_BR
dc.typeResumo em anais e proceedingspt_BR
dc.date.updated2017-03-29T11:11:11Zpt_BR
riaa.ainfo.id1066344pt_BR
riaa.ainfo.lastupdate2017-03-29pt_BR
dc.contributor.institutionALAN CARVALHO ANDRADE, SAPC; ORZENIL BONFIM DA SILVA JUNIOR, Cenargen; UFLA; CIRAD; DARIO GRATTAPAGLIA, Cenargen.pt_BR
Aparece en las colecciones:Resumo em anais de congresso (SAPC)

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