Your English writing platform
Discover LudwigSuggestions(1)
Exact(9)
As a consequence, the kernel trick allows the formulation of non-linear variants of any algorithm that can be formalized in terms of dot products.
This patient had clinical features of CHM (Fig. 2A); real time PCR analysis failed to show copy number variants of any of the exons of the CHM gene, but protein analysis confirmed absence of REP-1 (data not shown).
Interspersed among these clonal complexes were minor groups, typically joined doublets and individually unlinked STs that were not single-locus variants of any other STs in the database.
This approach is particularly suited for the analysis of tumor samples where gene re-arrangements and structural deviations can lead to novel variants of any gene [ 14].
M indT heG ap is the first integrated method to detect and assemble insertion variants of any size and any type, using modest computing resources.
We did not find any splice variants of any of the dynactin transcripts of the arthropods, although different splice forms exist for all of the mammalian dynactin subunits.
Similar(51)
That is, for the most part, we discuss variants of a read-any/write-any replication scheme.
But a variant of any of these candidate genes increases a person's risk of schizophrenia only a tiny amount.
In contrast to experimental studies, subjects of which are usually matching the primary interests of only a small minority of readers, case reports are of principle interest to all practicing neuropathologists, as any variant of any disease may be encountered by any neuropathologist at any time.
None of the 6 STs was a single-locus variant of any ST in the MLST database (i.e., sharing 6/7 alleles), but all in the database except ST904 had double locus variants (i.e., sharing 5/7 alleles) that were B. pseudomallei isolates from northern Australia.
When ASPicDB transcripts were included in the comparisons, the number of human genes with an orthologous splicing transcript in mouse rose to 4098, 4067, and 2838 for each of the three criteria, while 1283 (10%) of the human genes still remained without any RefSeq transcript with an orthologous splicing variant of any type in mouse.
Write better and faster with AI suggestions while staying true to your unique style.
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