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A mutation in genetic algorithm is used to prevent the local convergence of the algorithm.
These novel syndromes, combined with the ever-expanding literature on rare, one-off CNVs associated with disease phenotypes, highlight the significant involvement of CNVs as a causative mutation in genetic diseases.
This is generally achieved by calculating the ratio ρ/θ, which determines the relative frequency of occurrence of recombination and mutation events, and the ratio r/m, which measures the relative impact of recombination and mutation in genetic diversification.
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In that sense, students are challenged to think about new traits as arising due to multiple, random genetic processes, such as recombination of genes through sexual reproduction, gene shuffling and random mutations in genetic sequences (Garvin-Doxas and Klymkowsky 2008).
He made fundamental contributions toward elucidating the role of mutations in genetic disorders, and therefore was aware of the pain the parents of the affected children bear, and the misery that affected children endure.
Whole-genome sequencing represents a promising approach to pinpoint chemically induced mutations in genetic model organisms, thereby short-cutting time-consuming genetic mapping efforts.
Since then, the potential role of miRNA mutations in genetic diseases has been extensively investigated.
Such a question is best answered by loss-of-function mutations in genetic studies.
Cancer is a multistage progression process that results from mutations in genetic sequences.
The detection of mutations in genetic material is a major challenge for both genetic diagnostics and molecular genetic studies.
F1000Research: Dataset 1. Dataset for mRNA splicing mutations in genetic disease, 10.5256/f1000research.5654.d38248 The Splicing Mutation Calculator (SMC) is available at http://splicemc.cytognomix.com.
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