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During the first step, the predicted miRNA binding sites along with the 50-nt surrounding sequences at both ends were collected.
During the first step, the predicted sRNA binding sites along with the 50-nt surrounding sequences at both ends were collected in order to reduce the BLAST time.
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Sequences from the TS, RHS and DGF gene families annotated in the chromosome ends were collected from TriTrypDB and individually analyzed to search for transcripts.
Roots were washed under tap water to remove surrounding peat and approximately 1 cm of the root ends was collected for analysis.
Subsequently, 50 base pairs from each end were collected on the Life Technologies SOLiD3 or SOLiD4 instrument.
For stereology in mouse, coronal vibratome sections from the most anterior part of the telencephalon until its end were collected.
Exudate flowing from the bottom end was collected into sterile tubes placed on ice for several minutes.
For Dm, Ce, Nv, Dr, and Hs, ± 250 bp from the 5' annotated end was collected for each ortholog.
The end products were collected, from which five were selected, believed to be representative of the product of the 'good', 'satisfactory'modest'st'weakeand and 'very weak' writers.
Unmapped paired end reads were collected and mapped upon the genomic scaffolds of unmapped sequences from WAB56 104 using BWA mem with the default condition.
Asthma morbidity end points were collected quarterly.
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CEO of Professional Science Editing for Scientists @ prosciediting.com