Sentence examples for correct variant from inspiring English sources
When air is used for absorption, the steady-state measurement yields kLa values that correlate to the correct variant of the standard dynamic method.
Further, in some biological contexts, even in the absence of machine errors, BFAST would improve correct variant detection (such as highly polymorphic locations of the human genome like at the HLA locus).
Thus we are only evaluating the methods on their ability to find a correct CAL during the genome-wide global alignment, and not their ability to finish this with correct variant detection.
Making the correct variant classification is critical to the appropriate use of genetic testing in the clinical management of the patient and their family.
Expression of the correct variant protein was verified by matrix-assisted laser desorption ionization time-of-flight mass spectrometry as described previously.
Bioinformatic attempts to correct variant allele underrepresentation bring allelic ratios closer to unity and result in a higher number of mapped reads [ 33], but may not increase reliability of allelic ratio estimates [ 32].
There is also a checklist to ensure those medically important or other known to be correct variants that exhibit one of the above characteristics are not moved inadvertently to the failed variation table.
Although another program, Segminator II [ 11], can handle all three datasets as well, we consider the comparison would not be meaningful as in deep coverage data, it reports variants in every single position with respect to the reference genome and the burden of choosing the correct variants is left to the user.
Blue marks indicate the values obtained for RMAs set by our corrected variant prediction and orange marks indicate automated predictions by dbNSFP.
In this paper, two new corrected variants of AIC are derived for the purpose of small sample linear regression model selection.
The median of the three experiments was calculated and, in order to correct for variant frequencies in the genome, divided by the percentage of rups group related variants in the genome.
