On generalized competition index of a primitive tournament

AbstractFor positive integers k and m and a digraph D, the k-step m-competition graph Cmk(D) of D has the same set of vertices as D and an edge between vertices x and y if and only if there exist m distinct vertices v1,v2,…,vm in D such that there exist directed walks of length k from x to vi and from y to vi for 1≤i≤m. The m-competition index of a primitive digraph D is the smallest positive integer k such that Cmk(D) is a complete graph. In this paper, we study the m-competition indices of primitive tournaments and provide an upper bound for the m-competition index of a primitive tournament

Additional file 1: of Understanding the relationship between egg- and antigen-based diagnostics of Schistosoma mansoni infection pre- and post-treatment in Uganda

Detailed model description. Document explaining and justifying all model assumptions. Posterior distributions from the analysis are also shown, as well as the fit to the data. (PDF 2476 kb

Parasitological impact of 2-year preventive chemotherapy on schistosomiasis and soil-transmitted helminthiasis in Uganda-2

<p><b>Copyright information:</b></p><p>Taken from "Parasitological impact of 2-year preventive chemotherapy on schistosomiasis and soil-transmitted helminthiasis in Uganda"</p><p>http://www.biomedcentral.com/1741-7015/5/27</p><p>BMC Medicine 2007;5():27-27.</p><p>Published online 3 Sep 2007</p><p>PMCID:PMC2014753.</p><p></p>om eight districts for follow-up monitoring

Parasitological impact of 2-year preventive chemotherapy on schistosomiasis and soil-transmitted helminthiasis in Uganda-0

<p><b>Copyright information:</b></p><p>Taken from "Parasitological impact of 2-year preventive chemotherapy on schistosomiasis and soil-transmitted helminthiasis in Uganda"</p><p>http://www.biomedcentral.com/1741-7015/5/27</p><p>BMC Medicine 2007;5():27-27.</p><p>Published online 3 Sep 2007</p><p>PMCID:PMC2014753.</p><p></p>om eight districts for follow-up monitoring

Pfam domain families that are highly populated with allergenic protein sequences.

<p>Protein domain families considered for this analysis are highlighted in the box based on the families presented in the article co-authored by Fitzsimmons and Dunne [<a href="http://www.ploscompbiol.org/article/info:doi/10.1371/journal.pcbi.1004546#pcbi.1004546.ref021" target="_blank">21</a>].</p

Categorization of 10 protein domain families into groups.

<p>Categorization of 10 protein domain families into groups.</p

Distribution of allergenic molecules retrieved from Allergome database across Pfam domain families.

<p>Number of Pfam domain families with no allergenic members have also been represented. The Y-axis is scaled logarithmically (base 10), however true values are represented.</p

Venn diagram showing the distribution of Ab isotype responses to SmBv1L within IgG1, IgG4 and IgE responders in a population of 222 individuals endemically infected with <i>S</i>. <i>mansoni</i>.

<p>Venn diagram showing the distribution of Ab isotype responses to SmBv1L within IgG1, IgG4 and IgE responders in a population of 222 individuals endemically infected with <i>S</i>. <i>mansoni</i>.</p

List of the protein domain families/superfamilies that are populated predominantly with allergenic molecules.

<p>Total number of allergenic molecules (retrieved form Allergome database) in these families/superfamily and their ‘close homologs’ in eukaryotic metazoan parasites are shown.</p

Magnitudes of specific IgE, IgG4 and IgG1 responses to <i>S</i>. <i>mansoni</i> Bet v 1-like protein, SmBv1L, in a population of 222 individuals infected with <i>S</i>. <i>mansoni</i>, dotted lines indicate threshold of magnitude for a response.

<p>Data were normalized for expression on a log scale by the addition of constants so as to include zero values.</p