The phenotypic evaluation data showed a wide continuous distribution, with heritability values ranging from 0.58 to 0.84. Thirteen single nucleotide polymorphisms (SNPs) were identified, significantly associated with leaf scald resistance. Among these, eight were stable across multiple environments and ...
Seattle SNPs The Single Nucleotide Polymorphism database Glossary Atopy The propensity of an individual to develop allergic diseases, such as asthma, atopic dermatitis, food allergy or hay fever. It is defined operationally by elevations in serum levels of IgE reactive with allergens or by skin-...
Young AE, Bannasch DL: SNPs in the promoter regions of the canine RMRP and SHOX genes are not associated with canine chondrodysplasia. Anim Biotech 2008, 19:1-5.Young A E, Bannaseh D L. SNPS in the promoter regions of the canine RMRP and SHOX genes are not associated with canine ...
Furthermore, we found 4,311,814 SNPs with a minor allele frequency (MAF) larger than 0.05 (Figure S1; Table S3). In summary, more than 6 megabyte (MB) high-density and high-quality genotype data were obtained from 250 soybean accessions with a density of 1 SNP every 15 bases. ...
1 3Vol.:(0123456789) 3 252 Clinical and Experimental Medicine (2023) 23:3251–3264 Single-nucleotide polymorphisms (SNPs) in the ACE and ACE2 genes have been described, and their associa- tion with the risk of various diseases, included COVID-19 has been indicated [6]. In addition to ...
A total of 210 pQTL variants (16 non-redundant variants at LD r2 < 0.1 representing nine proteins; Supplementary Data 13) exactly matched SNPs associated with CHD from prior GWAS. Table 1 displays the sentinel pQTL variants that coincided with CHD-related GWAS SNPs and the corresponding ...
SNPs located in the coding regions of the spike and RNA polymerase proteins have been associated with the efficiency of the vaccines (COVID-19 Host Genetics Initiative, 2020). Intrahost single nucleotide variants (iSNVs) have also been reported in sequences of SARS-CoV-2, showing the ...
with candidate genes and non-synonymous SNPs within these genes highlighted in green. Coloured lines correspond to pairwise species comparisons (weighted mean; 10-kb window and 1-kb increments), and dots correspond to globalFSTvalues among the three species on a SNP basis. In all comparisons, ...
We also compared the new and known genes identified in our study. For all identified genes, we performed an enrichment analysis; for the genes identified using protein-coding SNPs, a functional analysis of protein-coding variants was performed; for the genes identified using non-coding SNPs, SMR...
The present invention is in the field of human disease diagnosis and therapy. The present invention specifically provides previously unknown single nucleotide polymorphisms (SNPs) in genes that have been identified as being involved in pathologies associated with human disease. The diseases/pathologies tha...