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In a Hilbert space, S. Takahashi and W. Takahashi [17] introduced the iteration as follows: sequence generated by, (1.3).
The same as follows Sequence saturation analysis is used to measure the sequencing data of a sample.
We confirmed the sequences for all the barcodes within the Barcoder collection by sequence analysis as follows (sequence data can be accessed at http://chemogenomics.med.utoronto.ca/supplemental/barflex/).utoronto.ca/supplemental/barflex/
The P-categories were randomly distributed in the allotment of three sets of categories as follows: sequence A, 130, sequence B, 122, and sequence C, 109.
The criteria used to select sequence fragments for validation were as follows: sequence fragments were more than 500 bp in length, included a detectable ORF (Olson 2002) and were composed of at least 50 reads.
The detailed results of the analysis are presented as follows: Sequence overview: the full sequence is shown with the positive aminoacids (those with exposure and quality values above the selected thresholds) highlighted in red.
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Following sequence mapping, differentially expressed genes were determined using tuxedo suite of programs including cuffdiff2 (version 2.2.1 64,65 with the optional parameter –library-type fr-firststrand.
Following sequence verification, the fragments were cloned into the pCAMBIA1301 binary vector (CAMBIA; www.cambia.org.au).au
Following sequence verification, DNA was transformed into AB1899 or DH5α strain of Escherichia coli.
Following sequence data collection, sequences were extracted using V4 forward and reverse primers.
Following sequence analysis of SAGE libraries, data were assembled in a unique matrix.
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