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The success of the method was evaluated using both out-of-bag (OOB) error and a small, fully-independent validation interpretation dataset.
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Routine clinical application of whole exome sequencing remains challenging due to difficulties in variant interpretation, large dataset management, and workflow integration.
The data mining and functional interpretation of datasets to access biologically interpretable results pose many analytical challenges, which have been recently reviewed by Kumar and Mann (2009).
The gene description, GO annotations were retrieved for each of the DEGs and were used for downstream interpretation of datasets.
Interpretation of the dataset is deferred to future papers.
Our interpretation of the dataset highlights the influence of the social factors and power dynamics on academic conferences.
Hence, it appears that our interpretation of the dataset is likely, and that other upwellings developed to the west of our featured upwelling.
As such, the proper interpretation of our dataset indicates that current chemotherapy and surgical therapies provided are equivalent at all facilities regardless of teaching status or volume.
However, interpretation of this dataset might not be applicable to complex disease genes since 97% of the disease genes were monogenic.
This, in no way, compromises the interpretation of our dataset.
In agreement with this interpretation, the resistant dataset is also enriched in strains with a "Small size" morphology.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com