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The different classes of children in our analysis define presentations of common infectious symptoms and are likely to represent those with different infectious exposure.
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Our analysis defined each influenza season as October 1 through May 31 of the subsequent year.
To cope with this, we instead used an adjusted dN/dS in our analysis, defined as dN/ dS+0.02).
A critical distinction is that our analysis defined H3K27me3-enriched regions before comparing the computed H3K27me3 signals between WT and Rest −/− ESCs.
The third transcription pattern of the long trajectory 1-5-7-8-10-12, as idefinesed by our analysis, defines the necessary "fine tuning" process towards cancerous phenotype.
Our analysis defined the highly conserved hydrophobic Trp333 within site 2 to be critical for Fz binding while it required several adjacent residues to induce full signaling.
Our analysis defined two genomic regions on Chr8 and Chr9 (Uns-7) containing loci responsible for high-level resistance, tc_ rph1 and tc_ rph2.
Our analysis defined the terminal bias as a dramatic rise in the number of statistically over-represented (z ≥ 3) C-terminal tripeptides (SOCTs) in the last 15 to 20 tripeptide positions of each "C-terminome".
Our analysis defines a catalog of human piRNA cluster candidates and sheds new light into the relationship between piRNAs and protein-coding genes, lncRNA genes, as well as mobile elements.
Our synteny analysis defined a multi-level gene organization in the bacterial chromosome.
Our phylogenetic analysis defines these three genes as a subgroup that has expanded during the evolution of vertebrates.
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CEO of Professional Science Editing for Scientists @ prosciediting.com