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Thus, through our alternative proficiency testing approach, we identified the bioinformatic detection of insertions/deletions as an area of particular concern for clinical laboratories performing next-generation sequencing testing.
We compared the phylogenetic informativeness of 959 UCE loci with a multi-locus data set of ten nuclear markers obtained via Sanger sequencing, testing the ability of these two types of data to resolve and date the evolutionary history of the second most species-rich subfamily of ants in the world, the Formicinae.
CIC and other toxicities need to be considered in drug selection, treatment sequencing, testing, and appropriate follow-up.
Myriad does not permit any biomedical researchers to perform full sequencing testing on those genes.
This newly identified mutation was not identified by standard Sanger sequencing testing due to its location deep within intron 1.
Such information may be of value to other health systems seeking to provide next-generation sequencing testing to their patient populations.
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Even for today's clinical sequencing tests, maintaining and communicating this information is difficult.
Since the family bought the sequencing tests themselves, they were not required to follow an Institutional Review Board IRBB).
The first column corresponds to the frontal sequences tested on the frontal classifier.
The first column corresponds to the frontal (F) sequences tested on the frontal classifier.
The HyperExon system outperformed leading splice recognition systems in the list of sequences tested.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com