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In terms of the delta, we obtained the same values for both datasets in all algorithm tests, with the exception of A l g Sign.
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To confirm that the cercomomad ITS sequences evolve significantly faster than any region of 18S rDNA sequence we constructed complementary alignments for both datasets in SE-AL using all available sequences derived from cultured representatives of the three cercomonad groups studied.
All findings on SSFP MRA were confirmed on CE-MRA datasets in all patients.
The method was also particularly robust in scenarios with a high proportion of patients who switched, and successfully gave a parameter estimate for all simulated datasets in all of the scenarios presented here.
We are delighted to announce the launch of GigaScience, an online open-access journal that focuses on research using or producing large datasets in all areas of biological and biomedical sciences.
Also, the models for Methods 5 and 7 converged for all the 1000 simulated datasets in all the scenarios (Tables 5 and 6, Additional file 3: Figures S1-S2).
The predictive ability is summarized with AUCmedian, and calculated as a pseudomedian over the left-out datasets in all the folds.
In both datasets, almost all genotypes were supported by bootstrap (BS) and PP values of >70 and >0.9, respectively.
Recombinant genomes were removed from the dataset in all subsequent analyses.
Analyses were also performed on the non-imputed dataset; in all presented analyses point estimates were similar as using the nonimputed dataset, with somewhat wider confidence intervals.
In conclusion, our method proves best on a difficult colon cancer dataset in all categories tested, raising accuracy beyond 90% as the only method in three test cases.
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