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Although resembling a breakdown of the broad-sense heritability, we describe each sequence of percentages formally as a diallel VarP because it uses out data to predict variance contributions in a perfectly balanced, complete, future diallel.
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This is an interesting paper about the role of sequence and percentage of eruption of first premolar in comparison to canine on development of crowding in the mandible.
An alternative measure of sequence variability, percentage of changes by species, was used to evaluate the most specific proportion of amino acid residues from alignments.
The number and type of aligned residues were used to classify the binding site local conservation, both in terms of sequence coverage (percentage of binding site residues in the original target that could be aligned to the pathogen sequence) and identity (percentage of identical residues among the aligned binding site residues).
As an indicator for the number of non-synonymous mutations (change of amino acid sequence) and synonymous mutations (no change of amino acid sequence), we determined the ratio of percentage nucleotide sequence identity to amino acid sequence identity.
aNumber of sequences (percentage of total) within which repetitive content was found.
For each slide, the mean and s.d. of copy number per cell of each tested DNA sequence, the percentage of cells with ⩽2, 3 and ⩾4 copies of each target and the ratio of MET/CEP7 and HGF/CEP7 were calculated.
Furthermore, in the literature, the bitrate control scheme generally fixes for the depth map sequence a percentage of 20% of the texture stream bitrate.
Here the range of nucleotide sequence identity percentages for each orthologous pair is between 16.54% and 100% (average identity, 53.27%).
For each subclass, a table describing consensus features (sequence, geometry, percentage of sequence identity, averaged RMSD and its standard deviation) can be obtained.
% of Finished Sequence Matched: the percentage of the span of finished sequence that is matched by contigs longer than 1 Kb.
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