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The deep split of the lineages investigated could suggest that the estimated constraint constitutes a representative average for birds.
The estimated constraint for 4-fold degenerate sites was 43.1% (±1.6%), 28.8% (±1.8%), and 24.2%±1.4.4%) in the chicken, turkey, and zebra finch lineages, respectively.
One way to handle this potential problem is to weight estimated constraint by the proportion of sequence removed in the neutral reference.
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Weighting the estimated constraints to take regions difficult to align in AR into account increases the estimates to 49.9% (±1.9%), 33.4% (±2.1%), and 28.0% (±1.6%), respectively.
For three-species alignments, we used the genome-wide divergence estimates obtained from concatenated sequences to directly estimate constraint as 1 − o/ e.
To widen the knowledge of selection at synonymous sites in vertebrates, we here estimate constraint at 4-fold degenerate sites of avian genes.
Estimating constraint from MSA has been widely applied to predict whether a sequence variant resulting in an amino acid substitution is likely to be deleterious.
If we use AR as a neutral reference to estimate constraint in the other sequence categories, 0-fold degenerate sites show an 86.7% (±0.6%) and 4-fold degenerate sites a 24.2% (±1.6%) constraint.
For example, the Genomic Evolutionary Rate Profiling (GERP) algorithm [ 31] is a widely used method for estimating constraint in genomic sequences as it can assign conservation scores to specific nucleotides, which is clearly of importance when annotating small-scale variation such as single-nucleotide variants (SNVs).
With the estimated PSM constraint for ST i (i =1,2,3,…,K) from DNPSM, we know the maximal allowed transmission power ( P i, j Max ).
Most studies that estimated evolutionary constraint on disordered regions have relied on interspecies comparisons using pairwise alignments of disordered regions across species.
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CEO of Professional Science Editing for Scientists @ prosciediting.com