3 research outputs found

    Selected region after second step of analysis for chromosome 4 (a), chromosome 8 (b), chromosome 16 (c), and chromosome 20 (d)

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    <p><b>Copyright information:</b></p><p>Taken from "Haplotype-sharing analysis for alcohol dependence based on quantitative traits and the Mantel statistic"</p><p></p><p>BMC Genetics 2005;6(Suppl 1):S75-S75.</p><p>Published online 30 Dec 2005</p><p>PMCID:PMC1866706.</p><p></p

    Phenotype Adjustments of the Study Group (392 Siblings)

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    <div><p>(A) Presence of asexual blood forms of P. falciparum in 31 weekly blood smears.</p><p>(B) Log of the 75th percentile of 31 parasite density values per individual.</p><p>(C) Median of 16 PCV assessments per individual.</p><p>(D) Malaria fever episodes were defined following WHO recommendations whereby multiple malaria attacks within 3 wk were considered recrudescences and counted as one episode (see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.0030048#s4" target="_blank">Materials and Methods</a>).</p><p><sup>#</sup>Gender did not significantly influence any of the phenotypes. For the phenotype of parasite density, the effects of antimalarial treatments were addressed by exclusion of density values following 3 wk after treatment (see <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.0030048#s4" target="_blank">Materials and Methods</a>). The phenotype of fever episodes was not corrected for the number of antimalarial treatments because of the direct causal relationship between disease episodes and treatments.</p><p><sup>§</sup>31 weekly regression models.</p><p><sup>*</sup>Anemia (PCV) was normally distributed, Shapiro-Wilk W test, <i>p</i> > 0.2.</p></div

    Quantitative-Trait, Multipoint Linkage Analysis of the Key Phenotypes of Uncomplicated Human Malaria

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    <p>(A and B) Parasitological phenotypes. (C and D) Clinical phenotypes. A 10k-Affymetrix SNP array was used for genotyping 377 individuals comprising 241 siblings of 68 families. Results obtained by NPL are presented in the upper panels (z scores [Z] on the left axis) and those of HE are presented in the lower panels (LOD scores [LOD] on the left axis). Empirical significance levels (<i>p</i>-values indicated by dotted lines) were estimated by 100,000-fold Monte-Carlo permutations.</p
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