scholarly journals Mapping Gene Associations in Human Mitochondria using Clinical Disease Phenotypes

2009 ◽  
Vol 5 (4) ◽  
pp. e1000374 ◽  
Author(s):  
Curt Scharfe ◽  
Henry Horng-Shing Lu ◽  
Jutta K. Neuenburg ◽  
Edward A. Allen ◽  
Guan-Cheng Li ◽  
...  
2021 ◽  
Vol 99 (Supplement_3) ◽  
pp. 235-235
Author(s):  
Jian Cheng ◽  
KyuSang Lim ◽  
Austin Putz ◽  
Anna Wolc ◽  
John Harding ◽  
...  

Abstract Disease resilience is the ability of an animal to maintain performance across environments with different disease challenge loads (CL) and can be quantified using random regression reaction norm models that describe phenotype as a function of CL. Objectives of this study were to: 1) develop measures of CL using growth rate and clinical disease phenotypes under a natural disease challenge; 2) evaluate genetic variation in disease resilience. Data used were late nursery and finisher growth rates and clinical disease phenotypes, including medical treatment and mortality rates, and subjective health scores, collected on 50 batches of 60/75 crossbred (LRxY) barrows under a polymicrobial natural disease challenge. All pigs were genotyped using a 650K SNP panel. Different CL were derived from estimates of contemporary group effects and used as environmental covariates in reaction norm analyses of average daily gain (ADG) and treatment rate (TRT). The CL were compared based on model loglikelihoods and estimates of genetic variance, using both linear and cubic spline reaction norm models. Linear reaction norm models fitted the data significantly better than the standard genetic model and the cubic spline models fitted the data significantly better than the linear reaction norm model for most traits. CL based on early finisher ADG provided the best fit for nursery ADG, while CL based on clinical disease phenotypes was best for finisher ADG and TRT. With increasing CL, estimates of heritability for ADG initially decreased and then increased, while estimates of heritability for TRT generally increased with CL. Genetic correlations were low between ADG or TRT at high versus low CL but high for close CLs. Results can be used to select more resilient pigs across different CL levels, or high-performance animals at a given CL level, or a combination of these. Funded by Genome Canada, Genome Alberta, USDA-NIFA, and PigGenCanada.


2009 ◽  
Vol 60 (2) ◽  
pp. 67-72 ◽  
Author(s):  
A.O. Akanji ◽  
J.U. Ohaeri ◽  
S.N. Al-Shammri ◽  
H.R. Fatania

2021 ◽  
Author(s):  
Matt Carland ◽  
Madhuchanda Bose ◽  
Biljana Novković ◽  
Haley Pedersen ◽  
Charles Manson ◽  
...  

The vast majority of human traits, including many disease phenotypes, are affected by alleles at numerous genomic loci. With a continually increasing set of variants with published clinical disease or biomarker associations, an easy-to-use tool for non-programmers to rapidly screen VCF files for risk alleles is needed. We have developed EZTraits as a tool to quickly evaluate genotype data (e.g. from microarrays), against a set of rules defined by the user. These rules can be defined directly in the scripting language Lua , for genotype calls using variant ID (RS number) or chromosomal position. Alternatively, EZTraits can parse simple and intuitive text including concepts like ' any ' or ' all '. Thus, EZTraits is designed to support rapid genetic analysis and hypothesis-testing by researchers, regardless of programming experience or technical background.


2016 ◽  
Vol 7 (1) ◽  
Author(s):  
Sirarat Sarntivijai ◽  
Drashtti Vasant ◽  
Simon Jupp ◽  
Gary Saunders ◽  
A. Patrícia Bento ◽  
...  

Until 2019, TBE was considered only to be an imported disease to the United Kingdom. In that year, evidence became available that the TBEV is likely circulating in the country1,2 and a first “probable case” of TBE originating in the UK was reported.3 In addition to TBEV, louping ill virus (LIV), a member of the TBEV-serocomplex, is also endemic in parts of the UK. Reports of clinical disease caused by LIV in livestock are mainly from Scotland, parts of North and South West England and Wales.4


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