Development and Validation of a 20K Single Nucleotide Polymorphism (SNP) Whole Genome Genotyping Array for Apple (Malus × domestica Borkh)

Publication Overview
TitleDevelopment and Validation of a 20K Single Nucleotide Polymorphism (SNP) Whole Genome Genotyping Array for Apple (Malus × domestica Borkh)
AuthorsBianco L, Cestaro A, Sargent DJ, Banchi E, Derdak S, Di Guardo M, Salvi S, Jansen J, Viola R, Gut I, Laurens F, Chagné D, Velasco R, van de Weg E, Troggio M
TypeJournal Article
Journal NamePloS one
Volume9
Issue10
Year2014
Page(s)e110377
CitationBianco L, Cestaro A, Sargent DJ, Banchi E, Derdak S, Di Guardo M, Salvi S, Jansen J, Viola R, Gut I, Laurens F, Chagné D, Velasco R, van de Weg E, Troggio M. Development and Validation of a 20K Single Nucleotide Polymorphism (SNP) Whole Genome Genotyping Array for Apple (Malus × domestica Borkh). PloS one. 2014; 9(10):e110377.

Abstract

High-density SNP arrays for genome-wide assessment of allelic variation have made high resolution genetic characterization of crop germplasm feasible. A medium density array for apple, the IRSC 8K SNP array, has been successfully developed and used for screens of bi-parental populations. However, the number of robust and well-distributed markers contained on this array was not sufficient to perform genome-wide association analyses in wider germplasm sets, or Pedigree-Based Analysis at high precision, because of rapid decay of linkage disequilibrium. We describe the development of an Illumina Infinium array targeting 20K SNPs. The SNPs were predicted from re-sequencing data derived from the genomes of 13 Malus × domestica apple cultivars and one accession belonging to a crab apple species (M. micromalus). A pipeline for SNP selection was devised that avoided the pitfalls associated with the inclusion of paralogous sequence variants, supported the construction of robust multi-allelic SNP haploblocks and selected up to 11 entries within narrow genomic regions of ±5 kb, termed focal points (FPs). Broad genome coverage was attained by placing FPs at 1 cM intervals on a consensus genetic map, complementing them with FPs to enrich the ends of each of the chromosomes, and by bridging physical intervals greater than 400 Kbps. The selection also included ∼3.7K validated SNPs from the IRSC 8K array. The array has already been used in other studies where ∼15.8K SNP markers were mapped with an average of ∼6.8K SNPs per full-sib family. The newly developed array with its high density of polymorphic validated SNPs is expected to be of great utility for Pedigree-Based Analysis and Genomic Selection. It will also be a valuable tool to help dissect the genetic mechanisms controlling important fruit quality traits, and to aid the identification of marker-trait associations suitable for the application of Marker Assisted Selection in apple breeding programs.

Features
This publication contains information about 18,019 features:
Feature NameUniquenameType
RosBREEDSNP_SNP_AG_9090256_Lg16_01730_MAF20_66683_exon1RosBREEDSNP_SNP_AG_9090256_Lg16_01730_MAF20_66683_exon1genetic_marker
RosBREEDSNP_SNP_AG_9121744_Lg3_RosCOS449_MAF10_491206_exon2RosBREEDSNP_SNP_AG_9121744_Lg3_RosCOS449_MAF10_491206_exon2genetic_marker
RosBREEDSNP_SNP_AG_9183120_Lg13_01742_MAF30_1674693_exon1RosBREEDSNP_SNP_AG_9183120_Lg13_01742_MAF30_1674693_exon1genetic_marker
RosBREEDSNP_SNP_AG_9267886_Lg5_01896_MAF50_1638631_exon5RosBREEDSNP_SNP_AG_9267886_Lg5_01896_MAF50_1638631_exon5genetic_marker
RosBREEDSNP_SNP_AG_9507490_Lg5_01781_MAF30_381189_exon1RosBREEDSNP_SNP_AG_9507490_Lg5_01781_MAF30_381189_exon1genetic_marker
RosBREEDSNP_SNP_AG_9544220_Lg3_02195_MAF50_1685314_exon2RosBREEDSNP_SNP_AG_9544220_Lg3_02195_MAF50_1685314_exon2genetic_marker
RosBREEDSNP_SNP_AG_9958893_Lg13_01507_MAF50_MDP0000263189_exon1RosBREEDSNP_SNP_AG_9958893_Lg13_01507_MAF50_MDP0000263189_exon1genetic_marker
RosBREEDSNP_SNP_CA_1010332_Lg3_00506_MAF10_1687129_exon1RosBREEDSNP_SNP_CA_1010332_Lg3_00506_MAF10_1687129_exon1genetic_marker
RosBREEDSNP_SNP_CA_10537812_Lg3_00194_MAF30_436195_exon1RosBREEDSNP_SNP_CA_10537812_Lg3_00194_MAF30_436195_exon1genetic_marker
RosBREEDSNP_SNP_CA_10597805_Lg11_00254_MAF20_16913_exon1RosBREEDSNP_SNP_CA_10597805_Lg11_00254_MAF20_16913_exon1genetic_marker
RosBREEDSNP_SNP_CA_1101058_Lg3_00866_MAF40_1635871_exon1RosBREEDSNP_SNP_CA_1101058_Lg3_00866_MAF40_1635871_exon1genetic_marker
RosBREEDSNP_SNP_CA_11386591_Lg14_02214_MAF40_765376_exon1RosBREEDSNP_SNP_CA_11386591_Lg14_02214_MAF40_765376_exon1genetic_marker
RosBREEDSNP_SNP_CA_11414678_Lg2_00159_MAF40_MDP0000320576_exon6RosBREEDSNP_SNP_CA_11414678_Lg2_00159_MAF40_MDP0000320576_exon6genetic_marker
RosBREEDSNP_SNP_CA_11451663_Lg2_00159_MAF50_331702_exon1RosBREEDSNP_SNP_CA_11451663_Lg2_00159_MAF50_331702_exon1genetic_marker
RosBREEDSNP_SNP_CA_11724861_Lg5_RosCOS544_MAF50_1621410_exon1RosBREEDSNP_SNP_CA_11724861_Lg5_RosCOS544_MAF50_1621410_exon1genetic_marker
RosBREEDSNP_SNP_CA_11958448_Lg17_01800_MAF30_98616_exon1RosBREEDSNP_SNP_CA_11958448_Lg17_01800_MAF30_98616_exon1genetic_marker
RosBREEDSNP_SNP_CA_1195935_Lg12_RosCOS3293_MAF30_1655383_exon1RosBREEDSNP_SNP_CA_1195935_Lg12_RosCOS3293_MAF30_1655383_exon1genetic_marker
RosBREEDSNP_SNP_CA_12059188_Lg17_00682_MAF10_MDP0000137984_exon6RosBREEDSNP_SNP_CA_12059188_Lg17_00682_MAF10_MDP0000137984_exon6genetic_marker
RosBREEDSNP_SNP_CA_12352575_Lg11_00441_MAF30_1646884_exon1RosBREEDSNP_SNP_CA_12352575_Lg11_00441_MAF30_1646884_exon1genetic_marker
RosBREEDSNP_SNP_CA_12364910_Lg16_01244_MAF50_MDP0000316202_exon4RosBREEDSNP_SNP_CA_12364910_Lg16_01244_MAF50_MDP0000316202_exon4genetic_marker
RosBREEDSNP_SNP_CA_12886110_Lg9_00331_MAF10_505681_exon2RosBREEDSNP_SNP_CA_12886110_Lg9_00331_MAF10_505681_exon2genetic_marker
RosBREEDSNP_SNP_CA_12919113_Lg8_01132_MAF20_324326_exon1RosBREEDSNP_SNP_CA_12919113_Lg8_01132_MAF20_324326_exon1genetic_marker
RosBREEDSNP_SNP_CA_13680239_Lg5_00978_MAF50_MDP0000255099_exon2RosBREEDSNP_SNP_CA_13680239_Lg5_00978_MAF50_MDP0000255099_exon2genetic_marker
RosBREEDSNP_SNP_CA_13921344_Lg2_248148__248148_exon1RosBREEDSNP_SNP_CA_13921344_Lg2_248148__248148_exon1genetic_marker
RosBREEDSNP_SNP_CA_14512918_Lg2_00002_MAF20_577821_exon1RosBREEDSNP_SNP_CA_14512918_Lg2_00002_MAF20_577821_exon1genetic_marker

Pages