Your English writing platform
Discover LudwigSuggestions(5)
Exact(11)
The percentage of nucleotide mutations (total number of mutations divided by total number of bases sequenced), amino acid mutations (total number of amino acid changes divided by total number of amino acids sequenced), and the sequence diversity (percent of clones with at least one difference from consensus) were used as indicators of genetic diversity.
fMinimum mutation frequency is the number of different mutations divided by the total number of nucleotides sequenced.
gMaximum mutation frequency is the total number of mutations (including repeated mutations) divided by the total number of nucleotides sequenced.
Specifically, in this study, the frequency was calculated as the number of recovered lethal mutations divided by the total number of F1 animals screened.
Let p(x i,j = 1) denote the number of unobserved mutations divided by the number of unobserved positions remaining in the matrix.
Mutation frequency was estimated as the total number of confirmed mutations divided by the total number of base pairs screened [ amplicon size - 200 bp) × individuals screened)].
Similar(49)
The elements of alternating rows contain mutation scores based on synonymous and non-synonymous mutations, which we define M ij _* (the wild card, * = non-synonymous/synonymous mutations (NSY/SY)) for gene i in sample j as the number of mutated bases, weighted by the functional impact score of this mutation, divided by the total number of bases that have sufficient read depth.
Thus, the probability π j 1 that the index case in family j was a BRCA1 carrier was given by: These probabilities were computed in MENDEL as the ratio of the likelihood of observing the family with the BRCA1 mutation divided by the likelihood of observing all possibilities.
To calculate mutation frequencies, the accumulated number of unique mutations were divided by the theoretical maximum number of the corresponding type of mutation so as to correct for base composition [30].
To assess mutation rates, the number of putative mutations was divided by the number of assayed bases for each library.
In our model, gene duplicates tend to buffer deleterious mutations (the coefficient selection of a mutation is divided by the copy number).
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com