Sentence examples for errors or absence from inspiring English sources

Exact(2)

The dissimilarities between sequences were in 89% (16 of 18 patients) date errors, or absence of coding for chemotherapy sessions (LED 21 51) or radiotherapy sessions (LED 1 3) at the start or the end of a state.

The dissimilarities between sequences were in 90% of cases related to dating errors or absence of coding for chemotherapy or radiotherapy sequences occurring at the start or at the end of a state.

Similar(58)

Estimation errors (or even absence of the statistics at hand), which will lead to a drop in the quality of recommendations.

Although the new HIS provides physicians with a function for prescription entry, inappropriate prescriptions can still be made due to system operation errors or the absence of updated patient information which is required for the consideration of contraindications.

Errors followed by reversals or absence of mutations could result in a descendant with the same phenotype as their ancestor.

While this also allows for the accumulation of error messages when several things go wrong, the presence or absence of errors is not visible at the type level and can only be determined upon inspecting the molecule's set of markers.

It can be deduced that Eq. (10) refers to the total probability of error or average probability of error in deciding the presence or absence of the primary signal.

Its implementation does not have to concern itself with the possibility of failure during parsing, and it is therefore not necessary to query the molecule for the presence or absence of errors.

The characteristics of the system dynamics are strongly determined by the presence or absence of errors (mutations in evolutionary terminology) in agents' decisions.

Furthermore, the subjects included in the analysis understood the task and were able to perform the task correctly, as indicated by their small number or absence of errors on the catch trials.

This could arise from either gestational loss due to LCAD deficiency as seen in the mouse model, a failure to recognize LCAD deficiency because the phenotype differs so greatly from other inborn errors of fatty acid metabolism, or absence of disease resulting from LCAD deficiency in humans [ 33, 34].

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