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Advances in molecular and genomic testing for patients with suspected infectious diarrhoea are on the horizon.
Genomic testing for KRAS and NRAS mutations in clinical biopsies of various cancers is routinely performed to predict futility of anti-epidermal growth factor receptor (anti-EGFR) therapies.
So in the next two years alone we'll deliver cutting-edge genomic testing for personalised cancer care, a 10% reduction in hepatitis C deaths, and advanced proton beam therapy.
Would Routine Genomic Testing For Cancer And Heart Risk Make Economic Sense?
Information-seeking and sharing behavior following genomic testing for diabetes risk.
As part of a study to understand the impact of delivery method of genomic testing for type 2 diabetes risk on comprehension and health-related behaviors, we assessed participants' information-seeking and sharing behaviors after receiving their results in-person with a genetic counselor or online through the testing company's website.
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WGS/WES should be considered a first-line genomic test for children with suspected genetic diseases.
The authors advocate the use of WGS or WES as a first-line genomic test for genetic disease in children.
Rather, WGS or WES should be considered a first-line genomic test for etiologic diagnosis of children with suspected genetic diseases.
The application of existing genomic tests for detecting deletions using coverage data were outside the scope of this paper as they typically require integration of information from the entire genome23,35.
Current guidelines state that CMA is the first-line genomic test for children with intellectual disability, developmental delay, autism spectrum disorder, and congenital anomalies.15,49,50,51,52,53,54,56,57,58 Since 2011, WGS and WES have gained relatively broad use for etiologic diagnosis of genetic diseases, but guidelines do not yet exist for their use.
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