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For samples recruited through EMBRACE, a pathogenic mutation was defined as an established disease-causing mutation under the classification scheme used by Breast Cancer Information Core.
A mutation was defined as a difference between the amino acid sequence of the studied virus and the wild type (HXB2) virus.
A somatic mutation was defined as a site that was consistently called homozygous in all BN cells (with a minimum of six read-coverage BN cells), but had mutant in less than three BC cells.
A pathogenic mutation was defined to be a variant that was predicted to result in a stop codon, a frameshift mutation, a large insertion or deletion, or a missense mutation previously reported in the scientific literature to be pathogenic.
IGHV mutation was defined by the presence of < 98% homology at sequencing and ZAP70 was defined as being positive if expressed in more than 20% of cells by flow cytometry.
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A dominant mutation is defined here as one mutated residue containing the largest sequence count compared with other residues at a particular aligned position.
Unlike the undefined and leaky panD2 mutation, the panD S25A mutation is defined and tight.
Mutation is defined as a sudden change that occurs in the genes of the offspring when compared to that of parent genes during the evolution process.
The genetic operators, crossover and mutation, are defined based on information gained about the feasible region and the behaviour of the objective function through the use of a data analysis procedure.
Another kind of DNA mutation is defined as "copy number variation".
A back mutation is defined as a mutation which increases the fitness of a genotype as in [ 8].
More suggestions(15)
transfer was defined
mutation was described
mutation was detected
mutation was repeated
mutation was confirmed
mutation was labeled
mutation was genotyped
mutation was created
mutation was backcrossed
mutation was introduced
mutation was expected
mutation was termed
mutation was found
mutation was named
mutation was identified
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