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Variants retained in the final B73 × CG dataset were required to have Phred ≥30, MQ ≥30, homozygous, opposite states in the parentals, ≥2× coverage in 20 F2 samples, heterozygosity ≥0.2 and ≤0.8 in F2, and mean r correlation ≥0.3 five variants upstream or downstream (Additional file 10).
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Obviously, a training dataset is required to determine the optimal DSEs.
It is important to note that the reference dataset is required to establish the hypothesis hierarchy and that it becomes part of the final network.
However, a σ or k value (to determine local σ i ), specific to the dataset, is required to be set optimally [42, 43].
Therefore, in our case, two passes on the dataset are required to detect the port scan attacks using the original version of CUSUM.
Compatible maps as well as an accurate, representative and comparable field dataset are required to obtain comparable and reliable estimates of map accuracy, but such datasets are usually not available.
This has benefited global public health and national health systems mainly through transparency and predictability of what scientific dataset is required to support the approval of a new pharmaceutical, hence advancing the innovation of drug development.
Each dataset was required to have at least three samples for both case and control groups.
Thus an extended dataset is required to better resolve the phylogeny.
Each constructed dataset was required to be of the same size as the original data based on estimated parameters and empirical predictors.
Such a dataset is required to develop a system level model which will facilitate better understating of the molecular aspects of embryo development in vitro.
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