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_TC_1213508_Lg5_01956_MAF20_MDP0000144375_exon2RosBREEDSNP_SNP_TC_1213508_Lg5_01956_MAF20_MDP0000144375_exon2genetic_marker
RosBREEDSNP_SNP_TC_12150935_Lg11_00240_MAF20_1637940_exon5RosBREEDSNP_SNP_TC_12150935_Lg11_00240_MAF20_1637940_exon5genetic_marker
RosBREEDSNP_SNP_TC_1215786_Lg12_RosCOS3293_MAF40_404415_exon1RosBREEDSNP_SNP_TC_1215786_Lg12_RosCOS3293_MAF40_404415_exon1genetic_marker
RosBREEDSNP_SNP_TC_1216653_Lg5_01956_MAF20_1658001_exon2RosBREEDSNP_SNP_TC_1216653_Lg5_01956_MAF20_1658001_exon2genetic_marker
RosBREEDSNP_SNP_TC_1218831_Lg5_01956_MAF30_1629562_exon8RosBREEDSNP_SNP_TC_1218831_Lg5_01956_MAF30_1629562_exon8genetic_marker
RosBREEDSNP_SNP_TC_1219423_Lg2_00348_MAF20_1649423_exon1RosBREEDSNP_SNP_TC_1219423_Lg2_00348_MAF20_1649423_exon1genetic_marker
RosBREEDSNP_SNP_TC_1229074_Lg2_01134_MAF10_1625597_exon3RosBREEDSNP_SNP_TC_1229074_Lg2_01134_MAF10_1625597_exon3genetic_marker
RosBREEDSNP_SNP_TC_12329007_Lg16_01244_MAF30_328549_exon1RosBREEDSNP_SNP_TC_12329007_Lg16_01244_MAF30_328549_exon1genetic_marker
RosBREEDSNP_SNP_TC_12334023_Lg16_01244_MAF50_1633206_exon1RosBREEDSNP_SNP_TC_12334023_Lg16_01244_MAF50_1633206_exon1genetic_marker
RosBREEDSNP_SNP_TC_12359661_Lg16_01244_MAF10_MDP0000311932_exon5RosBREEDSNP_SNP_TC_12359661_Lg16_01244_MAF10_MDP0000311932_exon5genetic_marker
RosBREEDSNP_SNP_TC_12362737_Lg16_01244_MAF40_MDP0000252150_exon5RosBREEDSNP_SNP_TC_12362737_Lg16_01244_MAF40_MDP0000252150_exon5genetic_marker
RosBREEDSNP_SNP_TC_12382050_Lg1_02334_MAF40_MDP0000219571_exon3RosBREEDSNP_SNP_TC_12382050_Lg1_02334_MAF40_MDP0000219571_exon3genetic_marker
RosBREEDSNP_SNP_TC_12433407_Lg10_00176_MAF20_1629673_exon1RosBREEDSNP_SNP_TC_12433407_Lg10_00176_MAF20_1629673_exon1genetic_marker
RosBREEDSNP_SNP_TC_12578927_Lg14_00170_MAF20_34257_exon1RosBREEDSNP_SNP_TC_12578927_Lg14_00170_MAF20_34257_exon1genetic_marker
RosBREEDSNP_SNP_TC_1282648_Lg10_RosCOS2296_MAF30_MDP0000226508_exon1RosBREEDSNP_SNP_TC_1282648_Lg10_RosCOS2296_MAF30_MDP0000226508_exon1genetic_marker
RosBREEDSNP_SNP_TC_12849756_Lg9_00331_MAF20_267702_exon1RosBREEDSNP_SNP_TC_12849756_Lg9_00331_MAF20_267702_exon1genetic_marker
RosBREEDSNP_SNP_TC_1312317_Lg9_02013_MAF30_484528_exon1RosBREEDSNP_SNP_TC_1312317_Lg9_02013_MAF30_484528_exon1genetic_marker
RosBREEDSNP_SNP_TC_1349777_Lg9_02013_MAF10_454625_exon1RosBREEDSNP_SNP_TC_1349777_Lg9_02013_MAF10_454625_exon1genetic_marker
RosBREEDSNP_SNP_TC_13528560_Lg4_RosCOS2954_MAF50_524827_exon1RosBREEDSNP_SNP_TC_13528560_Lg4_RosCOS2954_MAF50_524827_exon1genetic_marker
RosBREEDSNP_SNP_TC_13673501_Lg2_00214_MAF30_MDP0000235958_exon9RosBREEDSNP_SNP_TC_13673501_Lg2_00214_MAF30_MDP0000235958_exon9genetic_marker
RosBREEDSNP_SNP_TC_14081728_Lg4_01929_MAF30_MDP0000828295_exon1RosBREEDSNP_SNP_TC_14081728_Lg4_01929_MAF30_MDP0000828295_exon1genetic_marker
RosBREEDSNP_SNP_TC_14241533_Lg9_00958_MAF30_1654980_exon3RosBREEDSNP_SNP_TC_14241533_Lg9_00958_MAF30_1654980_exon3genetic_marker
RosBREEDSNP_SNP_TC_14329195_Lg5_02834_MAF10_MDP0000559762_exon1RosBREEDSNP_SNP_TC_14329195_Lg5_02834_MAF10_MDP0000559762_exon1genetic_marker
RosBREEDSNP_SNP_TC_14376292_Lg5_02834_MAF40_MDP0000184755_exon1RosBREEDSNP_SNP_TC_14376292_Lg5_02834_MAF40_MDP0000184755_exon1genetic_marker
RosBREEDSNP_SNP_TC_14450622_Lg3_01124_MAF30_1643213_exon2RosBREEDSNP_SNP_TC_14450622_Lg3_01124_MAF30_1643213_exon2genetic_marker

Pages