Exact(9)
"People always press me: 'Isn't there one marker we can use?' No.
Due to the addition of this marker, we can conclude that the previously suggested QTL is probably a false-positive.
Using the mutation status of each gene and the estimated response rates given a marker we can estimate the response rate of each patient in an approximate manner.
By use of a centering marker, we can ensure that the analyzed sections are those of tadpoles cut across the midline.
In this context, since we did not detect additional worsening in any systemic or regional tissue oxygen marker, we can assume that the reduction in sO2ER and mO2ER, in this model, is a salutary effect of HS.
Since observed heterozygosity and PIC rates are near the maximum theoretical values for a bi-allelic marker, we can conclude that the validation panel is highly informative for this type of markers.
Similar(51)
It is incremental: as we collect more semantics markers, we can verify more control flows.
What are the markers we can see for long-term problems?" The study received a $12-million 12-millionunding earlier this year from a Las Vegas dinner and auction.
In this case, using 25 markers we can achieve 79.4% classification accuracy, which improves to 97.4% using 50 markers.
It seems that, by adding more markers, we can get higher resolution without disturbing the framework of DFR typing.
With these markers, we can roughly distinguish mTECs and cTECs in immunofluorescence and flow cytometry assays.
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