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We evaluated all models with a corrected Akaike Information Criterion to determine which model represents the α-helices in the best way without overfitting the data.
Methods: We evaluated all adult patients in South Australia between 2004 and 2011 who survived hospitalisation requiring admission to a Public Hospital ICU.
We evaluated all 50 clinical and laboratory variables available on admission to critical care (day 1) (for a full list, see Additional file 1).
We evaluated all patients that presented to our ED as a diving accident from 1 November 2011 to 30 August 2015.
We evaluated all other brain regions outside primary and secondary a priori AOEs using a whole-brain Bonferroni correction.
We evaluated all associated CNV regions recurrent in MDD cases and exclusive with respect to controls (Table 1).
We evaluated all patients hospitalized in surgical, medical, oncology and haematology wards, as well as in the surgical and medical ICUs, excluding patients following lung transplantation.
We evaluated all substitution and indel variants detected by 454 and excluded repeat polymorphisms because of the possibility of false positive errors from PCR amplification [20].
To ensure that we evaluated all algorithms for their performance in detecting orthogroups across multiple species, we extended RBH and RSD into clustering algorithms (cRBH and cRSD, respectively).
In contrast, we evaluated all human miRNAs.
We evaluated all variables for nonnormality.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com