Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.

The SNPs that passed the genome-wide significance threshold (p , 5 6 10 28 ) in the EMMA mapping, using the 4Mil SNP panel, were then extracted and the nucleotide variant at

The objective of this study was to (i) fine map chro- mosomes that had QTL on our pig population: SSC1, SSC4, SSC7, SSC8, SSC17 and SSCX with increased marker coverage; and (ii) to

In this report, we describe a single nucleotide polymorphism (SNP) in the HvAACT1 coding region that was detected as T-1,198 (in genotypes with lower root growth on acidic soil)

The outbreak occurred on a farm located in an area endemic for fasciolosis, although the acute form of the disease is not common in cattle in this region.. It is likely that the

Because of the recent increases in the number of cases of acute Chagas disease in the Amazon region, it is important to consider this disease in the differential diagnosis of

Background: Recently, single nucleotide polymorphisms (SNPs) were identified in the promoter region of the perforin gene (PRF1) and it was found that the -398T mutant allele

Initiative for Chagas Disesae Surveillance and Preven- tion in the Amazon (AMCHA), officially launched under the auspices of the PAHO-WHO in 2004, public health researchers

A Mendelian Randomisation Study Where the Chosen Instrument Is in Linkage Disequilibrium with a Variant Associated With, or Causal For, the Disease Note that the direction of