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Dor, E.

Publications and source records attributed to Dor, E..

2 recordsLinked to original sources

Selecting Covariates for Genome-Wide Association Studies

The choice of which covariates to include in a Genome-Wide Association Study (GWAS) is important since it affects the ability to detect true association signal of variants, to correct for confounders and avoid false positives, and the running time of the analysis. Commonly used covariates include age, sex, genotyping batches, genotyping array type, as well as an arbitrary number of Principal Components (PCs) used to adjust for population structure. Despite the importance of this issue, there is no consensus or clear guidelines for the right choice of covariates. Therefore, studies typically employ heuristics for their choice with no clear justification. Here, we explore the dependence of the GWAS analysis results on the choice of covariates for a wide range of quantitative and binary human phenotypes. We propose guidelines for covariates choice based on the phenotypes type (quantitative vs. disease), the heritability, and the disease prevalence, with the goal of maximizing the statistical power to detect true associations and fit accurate polygenic scores while avoiding spurious associations and minimizing computation time. We analyze 36 traits in the UK-Biobank dataset. We show that the genotype batch and assessment center can be safely removed as covariates, thus significantly reducing the GWAS computational burden for these traits.

genetics↗

Isolation and characterization of a highly specific monoclonal antibody targeting the botulinum neurotoxin type E exposed SNAP-25 neoepitope

Botulinum neurotoxin type E (BoNT/E), the fastest acting toxin of all BoNTs, cleaves the 25 kDa synaptosomal associated protein (SNAP-25) in motor neurons, leading to flaccid paralysis. Specific detection and quantification of BoNT/E-cleaved SNAP-25 neoepitope is essential for diagnosis of BoNT/E intoxication as well as for characterization of anti-BoNT/E antibody preparations. In order to isolate highly specific monoclonal antibodies suitable for in vitro immuno-detection of the exposed neoepitope, mice and rabbits were immunized with an eight amino acid peptide composed of the C-terminus of the cleaved SNAP-25. Immunized rabbits developed a specific and robust polyclonal antibody response, whereas immunized mice mostly demonstrated a weak antibody response that could not discriminate between the two forms of SNAP-25. An immune scFv phage-display library was constructed from the immunized rabbits and a panel of antibodies was isolated. Sequence alignment of the isolated clones revealed high similarity between both heavy and light chains, with exceptionally short HCDR3 sequences. A chimeric scFv-Fc antibody was further expressed and characterized, exhibiting a selective, ultra-high affinity (pM) towards the SNAP-25 neoepitope. Moreover, this antibody enabled sensitive detection of the cleaved SNAP-25 in BoNT/E treated SiMa cells with no cross reactivity with the intact SNAP-25. This novel antibody can be further used to develop an in vitro cell-based assay to diagnose BoNT/E intoxication and to characterize antitoxin preparations, thus eliminating the use of animals in the standard mouse bioassay.

biochemistry↗