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PINK1 loss-of-function mutations are estimated to account for 1 7% of early onset PD (Tan et al. 2006).
In general, somatic BRCA1 and BRCA2 mutations are estimated to occur in 7% of all EOC [60]– [60].
Clinically significant BRCA mutations are estimated to occur in 1 in 300 to 500 persons in the general population [ 11].
The parameters for insertions, deletions and mutations are estimated by expectation-maximization (Baum-Welch algorithm) with no recombination (a conservative approach for detecting the effects of recombination).
Thus, BRCA2 mutations are estimated to confer a breast cancer risk which is similar to the population risk but 10 12 times greater.
Germline TP53 mutations are estimated to occur in no more than 0.25% of patients with breast tumors, regardless of family history [ 23- 25].
Similar(50)
In 1997, the lifetime risk of breast cancer in women with BRCA mutations was estimated in the range of 85percentt.
As a result, a woman with one of those mutations is estimated to have a 60%to70%0% chance of developing breast cancer at some point in her life.
Therefore, the lower limit of detection of minor resistance mutations was estimated to be 0.5 3.0% in the previous studies [12], [18], [19], [30], [31].
The fractions of sites in the coding regions for synonymous, nonsynonymous, and nonsense mutations were estimated to be 28.5%, 68.1%, and 3.4%, respectively.
In women with early-onset breast carcinoma unselected for family history, the prevalence of BRCA1 mutations is estimated to be between four and nine percent [16] [23].
More suggestions(15)
mutations are summarized
mutations are known
mutations are seen
mutations are observed
mutations are highlighted
mutations are sequenced
mutations are underlined
mutations are introduced
mutations are kept
mutations are summarised
mutations are replicated
mutations are identified
mutations are termed
mutations are mapped
mutations are assumed
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