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Both matK and the nuclear 26S rDNA have been informative in large-scale angiosperm phylogenetic studies (e. g., matK: [ 10, 22, 23]; 26S rDNA: [ 29- 32]), and consequently, sequence data from both genes are available for many angiosperm taxa.
Consequently, sequence {G x,x,u n ) + G y,y,v n )} is non-negative and decreasing, so G ( x, x, u n ) + G ( y, y, v n ) → g, for some g ≥ 0. We claim that g = 0. Indeed, if g > 0 then following similar arguments to those given in the proof of Theorem 3.1, we conclude that θ ( G ( x, x, u n - 1 ), G ( u n - 1, y, y ) ) → 1.
Consequently, sequence modifications can cause a change in the seed region and affect the target repertoire of particular miRNA.
Consequently, sequence alignments can provide hints at the optimal structure-based alignment, but are potentially far-off.
Consequently, sequence differences between its genome and that of the reference used to design the arrays may result in some probes failing to hybridise to their target sequence.
Consequently, sequence variation among the 36 clinical P. aeruginosa strains was markedly increased (dN = 3.5 × 10-3) for genes belonging to these regions of genomic plasticity (RGPs, [ 21]).
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Genes from positive colonies were consequently sequenced.
Next, using these genes, we analyzed the mRNA diversity and consequently sequenced and identified 11 769 human full-length cDNAs whose predicted open reading frames were different from other known full-length cDNAs.
Two of the nine genes, SEC63 and FOXO3, encompassed by the common region of deletion were underexpressed in IMPC cases (P ≤ 0.05 by Welch test, fold change ≥1.5, real-time quantitative RT-PCR) and were consequently sequenced.
In other words, our workflow detects motifs that represent the consensus of mutually exclusive subsets of pooled sequences, and the motifs consequently represent sequence subsets that could be very different.
One of these environmental sequences, namely DH148-5-EKD18 is highly divergent and was sharply separated from other sequences in some of the earliest environmental DNA surveys; consequently, this sequence was interpreted as a novel, early-branching, "higher-level to new-kingdom level" taxon [1], [4], [12] [13] that was subsequently affiliated with parabasalids [15].
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