CIMMYT Ethiopia
HTMA MPS2 Cycle 2 genotyping for GEBV estimation
Cycle 2 formed by inter mating selected Cycle1 genotypes genotyped with 93 SNPs for GEBV estimation for grain yield
1 resource
Published 6 Feb 2017
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Agricultural data for Ethiopia, gathered from research institutes and government sources into one searchable catalogue.
1–7 of 7 datasets
CIMMYT Ethiopia
Cycle 2 formed by inter mating selected Cycle1 genotypes genotyped with 93 SNPs for GEBV estimation for grain yield
CIMMYT Ethiopia
Cycle 1 formed by inter mating selected S2 families genotypes genotyped with 84 SNPs for GEBV estimation for grain yield
CIMMYT Ethiopia
Cycle 2 formed by inter mating selected Cycle1 genotypes genotyped with 93 SNPs for GEBV estimation for grain yield
CIMMYT Ethiopia
Cycle1 formed by inter mating selected S2 families genotypes genotyped with 84 SNPs for GEBV estimation for grain yield
CIMMYT Ethiopia
Genetic profiling of wheat breeding lines from the CIMMYT bread wheat breeding program was carried out over several years.
CIMMYT Ethiopia
DArTAG panel 2 validation data on 1454 CIMMYT spring bread wheat elite lines included in the 53, 54 and 55IWBWSN and 38, 39 and 40 SAWSN. DArTAG panel 2 consists of 3897 selected SNPs.
CIMMYT Ethiopia
The historic crossing block (HCB) is a collection of all the parents of spring wheat pre-breeding crossing block that include landraces, synthetics, synthetic derivatives, elite lines, high biomass lines, lines with rust resistance, and some varieties. Every year, to incorporate novel alleles into elite back grounds several strategic crosses-source× sink, landrace × elite, synthetic × elite-are made based on the physiological breeding approach (Reynolds et al. 2017b). The HCB is comprised of three panels: germplasm used for the crosses for yield potential (CB-YP), drought (CB-D), and heat stress (CB-H). The number of lines in each panel increased from 128 to 311 in CB-YP, from 123 to 219 in CB-D, and from 80 to 195 in CB-H during 2012-2017. A total of 119,144 SNP markers were identified on the germplasm. After quality control (removing markers with missing data > 30%, and minor allele frequency < 5%), 13135, 11717, and 14441 polymorphic SNPs for CB-YP, CB-D, and CB-H, respectively were used for further analysis.