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Prior to data analysis, the sequence reads from this dataset were sorted by MID-tag into the original four libraries.
For rank analysis, peaks from the final dataset were sorted by peak rank (calculated by Cisgenome package and dependent on read count as a measure of interaction strength) and divided into 10 bins.
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Each virus was assigned a unique identification number, allowing us to link geographic location, genetic sequence and temporal data in later analyses, and the dataset was sorted in ascending order by this unique ID.
Datasets were sorted into groups by type of imaging, which were then subdivided by target of evaluation (per-patient or per-segment).
Thus oligomers were sorted by zero-order Markov model rank, as this dataset is further restricted by oligomers per megabase whereas the second-order Markov model dataset is not.
Thereafter, data files were sorted by their identification variables and the four cross-sectional datasets of 1993, 1998, 2003 and 2008 09 were merged into a single data file.
The manually clustered websites were sorted by the date each website was identified, and then both datasets were divided into training and testing populations of 80%and20%0%, respectively.
Next, genes were sorted by corresponding property value, and 209 gene sliding windows were examined across each dataset.
(C) Inflammatory cells were sorted by FACS.
Samples were sorted by overall mutational burden.
Then, these cells were sorted by FACS.
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CEO of Professional Science Editing for Scientists @ prosciediting.com