The genetic architecture of resistance and susceptibility to virulent ovine footrot was studied in a cohort of 3,208 animals from 37 informative flocks of predominant Merino (93%), and Merino Types (Poll Merino, Dohne and South African Meat Merino). Footrot was scored as a binary trait where an animal was scored as affected (1) or unaffected (0, free from footrot), after 2 known challenges. For final analysis, animals from flocks with a prevalence in the range of 30-70% were selected. Animals were genotyped with either a 50K or 15K SNP panel on the Illumina Ovine bead array resulting in combined imputed SNP genotype for 51,713 markers for all animals. The animals were of mixed ages (lambs, yearlings, hoggets and adults), sexes, and breeds. Heritability of footrot was 0.39 ± 0.04 based on a genomic relationship matrix on the underlying scale. Corresponding proportional chromosome heritabilities were in the range of 0.00 ± 0.01 (OAR12) to 0.14 ± 0.04 (OAR23) and compared against expected based on chromosome length. Two markers on OAR23 accounted for a significant component of the additive genetic variance, whilst all residual SNP markers failed to reach statistical significance, despite being located on chromosomes with disproportionate effect on the genetic variance. The polygenic nature of genetic variation in resistance to footrot is discussed.

Hanwoo is highly prized for its marbling ability and is the most important cattle breed in Korea. In order to maintain the integrity of the breed and for product certification purposes it is important to develop tools to confirm the origin of the products. Breed composition estimates based on a large number of molecular markers (e.g. HD SNP arrays) are highly accurate but expensive for routine usage. The identification of a reliable panel with a small number of markers will reduce costs and can enable broader adoption of the technology by industry. In this work a heuristic optimization method was used to find the most reliable subset of markers, from the Illumina BovineHD array, to estimate breed proportion in Hanwoo. Accuracies of breed proportion estimates above 90% can be achieved using as little as 200 markers. The best balance between accuracy and number of SNP was obtained with 500 markers achieving 94% accuracy. Rapid and cost effective breed composition prediction in Hanwoo cattle based on a SNP panel with at least 200 markers will help to certify the products with an acceptable accuracy and ensure breed purity within the breeding program. The method described herein is directly applicable to other breeds.

Background: Smallholder dairy farming in much of the developing world is based on the use of crossbred cows that combine local adaptation traits of indigenous breeds with high milk yield potential of exotic dairy breeds. Pedigree recording is rare in such systems which means that it is impossible to make informed breeding decisions. High-density single nucleotide polymorphism (SNP) assays allow accurate estimation of breed composition and parentage assignment but are too expensive for routine application. Our aim was to determine the level of accuracy achieved with low-density SNP assays.

Methods: We constructed subsets of 100 to 1500 SNPs from the 735k-SNP Illumina panel by selecting: (a) on high minor allele frequencies (MAF) in a crossbred population; (b) on large differences in allele frequency between ancestral breeds; (c) at random; or (d) with a differential evolution algorithm. These panels were tested on a dataset of 1933 crossbred dairy cattle from Kenya/Uganda and on crossbred populations from Ethiopia (N = 545) and Tanzania (N = 462). Dairy breed proportions were estimated by using the ADMIXTURE program, a regression approach, and SNP-best linear unbiased prediction, and tested against estimates obtained by ADMIXTURE based on the 735k-SNP panel. Performance for parentage assignment was based on opposing homozygotes which were used to calculate the separation value (sv) between true and false assignments.

Results: Panels of SNPs based on the largest differences in allele frequency between European dairy breeds and a combined Nelore/N'Dama population gave the best predictions of dairy breed proportion ( r² = 0.962 to 0.994 for 100 to 1500 SNPs) with an average absolute bias of 0.026. Panels of SNPs based on the highest MAF in the crossbred population (Kenya/Uganda) gave the most accurate parentage assignments (sv = -1 to 15 for 100 to 1500 SNPs).

Conclusions: Due to the different required properties of SNPs, panels that did well for breed composition did poorly for parentage assignment and vice versa. A combined panel of 400 SNPs was not able to assign parentages correctly, thus we recommend the use of 200 SNPs either for breed proportion prediction or parentage assignment, independently.

To detect how much genetic variance is accounted for by different genomic regions one first step is to work at the chromosomal level. We used a half sib data structure for two growth traits in sheep as a potentially powerful design to partition the genetic variance across chromosomes. Records for post weaning weight (PW) and scan C site back fat (CF) were used from 5,239 merino sheep. The model of analysis accounted for population structure by fitting genetic group effects as well as the numerator relationship matrix (A) or the first five principal components (PC). Different approximations were compared fitting the genomic relationship matrix (0) based on 48,599 markers, or on single nucleotide polymorphisms of an individual chromosome. The correlation between chromosome length (L) and variance explained per chromosome (uJ) was 0.53 and 0.70 for PW and CF correspondingly, however significant differences in (uJ/L) were found between chromosomes, ranging from 0% to 17.5%. Some chromosomes explained more variance and covariance than expected, under the assumption that it is proportional to the chromosome size; suggesting that some chromosomes clearly harbor more QTL. Some chromosomes show a covariance of opposite sign indicating they could be used in selection to 'break' an unfavourable correlation (e.g. chromosome 8). These results represent a powerful source of information for genomic selection.