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However, our genomic analysis reveals no homologs of comQXPA genes in the P. polymyxa genomes, which may explain the low transformation frequency of CR1 compared to B. subtilis (our unpublished data).
The Ae. tauschii genome has the largest number of pseudogenes among all examined genomes, which may be attributable to historical bursts of TE activity.
Their success is a first step toward a new way to edit genomes, which may not only aid our understanding of how life works, but also may prove useful when genome changes are needed to cure disease.
The Bcc have large, metabolically diverse, and plastic genomes which may explain their ability to live in such diverse environments.
Here we demonstrate the utility of TASR for discriminating real from artifactual variant calls in tumour genomes, which may facilitate large-scale validation efforts.
This result suggested that, although most genome sequences and gene contents are conserved among pseudomonads, many inversion incidents occurred in Psg genomes, which may represent the genetic diversification within the Psg population.
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The genomic island contained a terminal transposase (the only transposase gene found throughout the genome), which may facilitate HGT of the genomic island containing tetracycline resistance genes enhancing the virulence of C. suis R19 (Donati et al. 2011).
In addition to providing Prillinger and her family with crucial information about their personal health, the results could reveal undiscovered information related to the condition encoded in the human genome, which may enable the expansion of current tests.
Lentiviral delivery is currently among the most efficient methods but it integrates transgenes into the genome, which may affect the behavior of the iPSC if integration occurs into an important locus.
The event R450-5 may have multiple copies of insert in its genome, which may explain the lack of negative segregates in its T1 population.
For example, the Genome Control method [20] assumes that the degree of population differentiation is the same throughout the human genome, which may not the case.
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