Exact(4)
The data was then condensed into contingency tables and evaluated using summary statistics and odds ratios.
We then applied the ndLP and rLP techniques using the glpk solver (see Methods) to these tables and evaluated the total running time.
BZ, MG, and DS conducted the analyses, constructed summary of findings tables, and evaluated the quality of evidence using the GRADE approach.
Qualitative data in the 2 groups were expressed as frequencies, organized into contingency tables, and evaluated with the [chi]2 test (Pearson [chi]2 test or Fisher exact test) to investigate potential differences.
Similar(56)
We compared the consensus genotypes from the DOP-1, MDA-2, MDA-3, and MALBAC deep-sequenced data with the corresponding golden controls (Table 2 and Additional file 13: Table S7), and evaluated the consensus genotypes detection efficiency (CGDE) and concordant ratio (Methods).
Accordingly, we identified a set of 30 predominantly late-stage MSS Caucasian CRC cases from the TCGA WES cohort (Additional file 1: Table S1), and evaluated for significant sCNAs (ENVE P ≤ 0.05; Additional file 1: Table S3) followed by GISTIC analysis to identify recurrent chromosomal arm-level alterations (q ≤ 0.25; Additional file 1: Table S6).
We report the number and total size of the configuration messages to be sent (Table 5) and evaluated how long the processing of the samples takes on the node (Table 5).
To discern a role for environmental phages in the B. anthracis lifecycle, we infected ΔSterne with several phages from Table 1 and evaluated phenotypes of the resulting lysogens.
We collected longitudinal CSF and plasma samples from 104 ALS and control subjects (Table 1) and evaluated the absolute cystatin C concentrations by ELISA and the total sample protein concentrations by BCA protein assay.
To examine if antibody responses differ according to disease stage, we studied a cohort of 21 patients diagnosed with stage I, II, III and IV melanoma (Table 1) and evaluated the reactivity of antibody cultures (n = 1,800) from these patients to the metastatic melanoma cell line A-375 utilizing the cell-based ELISA.
The 18 chemicals were combined according to a specified mixing ratio (Table 2) and evaluated experimentally.
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