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Rotational twin martensite variants were discovered to be related with an angle rotation of 15° in the [1 1 1] direction.
However, copy number variants were discovered to be present and widespread in the genome shortly thereafter[10], [11].
A total number of 16 rare non-synonymous variants were discovered, 13 of which are exclusive in cases and 3 exclusive in controls.
Thirteen variants were detected in the control group compared with eleven variants in the affected breast cancer cohort; of these, 9 unnamed, novel variants were discovered in sum.
Among the variants detected, 9 novel variants were discovered and 2 were found to be associated with the susceptibility of breast cancer.
Novel variants were discovered and characterized in terms of size, minor allele frequency, type of polymorphism (gains, losses or both), and mechanism of formation.
Similar(26)
The more harmful genetic variants are discovered, the more compelling the logic may seem of fixing the bugs in the genomic programming directly instead of treating the symptoms in each generation, a procedure called germ-line gene therapy.
However, as BChE variants are discovered and developed, a generic purification protocol that is insensitive to amino acid substitutions is necessary.
As more variants are discovered, it is natural to ask: what is the total number of susceptibility variants that underlie these complex diseases?
We also propose that the first full-length "known" subunit splice variant should be named "v1", allowing for subsequent addition and standard nomenclature if additional variants are discovered in the future.
(Since we assume 3 significant markers per causal variant, when all the causal variants are discovered with large enough sample size, the top 1000 SNPs will in the average contain the top 333 causal SNPs).
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