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This suggests that transcriptome alterations may not be fundamentally based on protein expression levels or insert complexity, but instead could be due to the attributes of the specific recombinant protein being expressed, mutations/disruptions from the insertion of T-DNA, or some combination of both.
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Prior to sequencing, library insert size and complexity were evaluated as described in Rise et al. [ 20].
Interestingly, we and others ([ 22, 27]; our unpublished results) have observed that there is a strong selection against low complexity inserts within core secondary elements of secondary structures of P. falciparum proteins.
A subset of the families or members within each family might show certain peculiarities: the eukaryotic versions of the CDC123 family are often characterized by large, variable, low complexity inserts within the catalytic module predicted to be structurally disordered.
Preliminary assessment of library quality indicated that the larval library had fewer clones without inserts and higher complexity than the other two libraries, so the majority of ESTs were sequenced from this library.
This led to the identification of several homologs with probably the same function, generally with amino acid compositional biases and the occurrence of low complexity inserts in the Plasmodium genes.
Using the pNubG-x vector, prey from a mouse adult brain library (average insert size 1.3 kb, complexity 3×10) was expressed as a fusion to a mutated N-terminal half of ubiquitin (NubG).
Despite a lower library complexity, large insert MP libraries (20 or 25 kb) provided very high physical genome coverage and were found to efficiently span repeat elements in the genome.
Finally, implant performance is potentially confounded by the technical difficulty of inserting the implant, the knowledge and abilities of the surgeon inserting them, and the complexity of the cases.
With the same complexity, the inserted delay in Kuo's two-tap adaptive filter can be moved back to construct the proposed approach, which would achieve a better performance.
As this combination of datasets is currently not available for human we generated a modified reference sequence from the human reference genome hg19 (limited to chromosomes 1 and 2 to reduce computation time without reducing complexity) by inserting a representative set of TE sequences at random locations, excluding already annotated TEs and regions of Ns.
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