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Next, these templates were analyzed in three different scales using wavelet transform to separate vessels according to their diameter sizes.
The morphology and microstructure of the Si NWs grown over AAO templates were analyzed by FESEM Philipss, FEG-XL30S, 20 kV, Philips Electronic Instruments Co., Chicago, IL, USA) and by high-resolution transmission electron microscopy (HRTEM, JEOL JEM-3000F, JEOL, Tokyo, Japan).
There was very little variation in HRM scores obtained when the same DNA templates were analyzed repeatedly over the course of a year (intra-class correlation coefficient: 94% [95% CI: 89%, 98%]) [21].
The templates were analyzed at 1 1 and 1 10 concentrations, and reactions were duplicated.
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These templates are analyzed using two classifiers.
The generated pool of DNA templates is analyzed in a cell-free expression screen and the most efficient template is selected for further preparative scale protein production.
In the next stage, these templates are analyzed in three different scales using wavelet transform to separate vessels according to their diameter sizes.
The sequences of the ESTs (with vector sequence trimmed off, as recombinant plasmids were used as template) were analyzed for their homology against the publicly available non redundant genes/ESTs/Transcripts in the NCBI database using the BLASTN and BLASTX algorithms [85], [86], [87], [88].
The three types of template were analyzed separately by combined bisulfite restriction analysis (COBRA).
For a given cluster, the multiple sequence alignment pertaining to the respective cluster and two-protein alignment between the query and modeling template were analyzed.
The HA powder obtained from co-precipitation during the synthesis (not attached to porous template) was analyzed by XRD and Raman spectroscopy, and its morphology/crystalline structure was determined by TEM. Figure 2a shows the XRD spectrum of the HA powder sample obtained with the method discussed above.
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