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Thus, these genes are expected to be expressed when and where the Fe requirement is elevated.
The location of the threshold suggests that the introduced genes are expected to spread in space, at least locally.
Because housekeeping genes are expected to have much higher germline expression levels than narrowly expressed somatic genes, transcription-associated deletion bias is not supported.
Furthermore, the threshold for the gene frequencies over which the introduced genes are expected to become fixed upon discontinuing the release of transgenic individuals is surprisingly low.
Multiple genes are expected to contribute to this variation.
Such genes are expected to diverge from each other extremely rapidly.
As demonstrated for other two-component systems, multiple genes are expected to be under the control of BvrR/BvrS [1].
Additionally, given that the splicing machinery is not 100% efficient, all genes are expected to produce some aberrant mRNA isoformes [52].
The priority of selection assigned to the sensitivity in detecting expressional changes, since the magnitude of differences and the number of affected genes are expected to be limited.
Additional copy number variants and less common biallelic variants within LPA and other genes are expected to contribute to the remainder of the variance.
However, the precise molecular pathogenesis of this heterogeneous disease remains poorly characterized, and more T2D-related genes are expected to be uncovered.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com