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In one of the largest analyses of diet and various types of arthritis, researchers looked at data on more than 800 patients from 15 studies.
Ours is the largest analyses to date to examine the association of variation in any CRP SNP or haplotype with CHD (we examine association with one SNP rs1130864); our analysis includes 18,637 participants with 4,610 CHD cases.
Only one of the largest analyses of HapMap LCL samples was included here [ 27], and drug response, methylation, miRNA and non-human eQTL studies were excluded.
It is one of the largest analyses of the phenomenon of inpatient hypoglycemia, encompassing >4,300 admissions of 2,582 individual patients.
The current studies are the largest analyses to date that have examined the risk of HZ in patients with RA treated with tofacitinib, a JAK inhibitor for RA.
Indeed, Karapetis and colleagues reached the conclusion that additional biomarker approaches are needed to identify KRAS-wildtype patients who will receive benefit from cetuximab in one of the largest analyses to date of the association of KRAS status with clinical outcome to cetuximab in CRC [ 7].
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We included P. fasciculata, P. involucrata, P. sikkimensis and P. alpicola in the larger analyses to obtain a root age estimate for Primula sect.
Sequence data from 74 species were included in the large analyses (see Table 3 for all species names and accession numbers).
The sample sizes (24 and 22 respectively) used for the mating-type distribution analyses are relatively small compared to the larger analyses within this paper, therefore, firm conclusions cannot be drawn.
This study represents one of the larger analyses undertaken to date comparing the EQ-5D and SF-6D and suggests that the EQ-5D may be the more appropriate technique for measurement of utility values in severe chronic pain.
Considering the ~50% observed frequency of missense mutations and assuming that 25% of them are deleterious, we have calculated that on average, 1774 TILL er lines are sufficient to obtain 20 mutations per ~1 kb gene fragment, while the larger analyses carried out until now are providing additional truncation mutations for ~90% of the genes.
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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