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However, considerable heterogeneity exists within both types of regions.
Both types of regions were found in A673 and SK-N-MC cell lines (Fig. 1B), indicating that neither type of region was cell specific.
Eleven exons were derived from LTR element internal sequences and 3 exons contained both types of regions.
§ T-test for paired samples (unique vs. repetitive) on proteins having both types of regions [ABD-A, LAB, PB, BCD, ZEN, Ccp84Ac, CG13617, CG14290 and LAP (product of CG2520)].
The T-test for paired samples (unique versus repetitive) on proteins having both types of regions showed significant differences between unique and repetitive sequences (P = 0.001), the mean of repetitive sequences being more than twice that for unique sequences (51.01% versus 23.19%, respectively).
We also calculated the proportion of amino acid differences and indels in repetitive and non-repetitive (unique) sequence in the three groups, and tested for differences between these two types of regions using a T-test for paired samples [ 82] on those proteins having both types of regions.
Similar(53)
Consequently, the calculations assume that the distribution of log2ratio is Gaussian for both types of region and no attempt is made to account for possible autocorrelation between data points mapping to nearby genomic locations.
Both types of functional regions are the non-coding regions from the published results of the ENCODE project [ 22, 23].
Frequency analysis of the surface pressure fluctuations shows broadband spectra at many locations under both types of separation regions.
Both types of amorphous regions can be considered as interphase components with similar characteristics to the liquid-like and crystalline components, respectively.
In this paper we aim to more fully characterize the structural embedding of both types of hub regions in brain networks and to determine whether our results can be extended beyond the brain of a single species.
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