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Molecular diagnosis of specific target bacteria DNA sequences is then performed using a realtime loopmediated isothermal amplification (RTLAMP) with SYTO-9 as the signal reporter.
The ASD between the original and quantized LSF vector sequences is then calculated.
The binary integer programming problem for subcarrier and bit allocation for FGS encoded video sequences is then formulated as (1).
A difficulty with using Walsh codes in terms of their correlations (compared to PN sequences) is then presented, as well as a discussion on how to overcome it.
With reads of a length of ≈100 bp excluding primers, and primers of length 22 bp, the expected proportion of non-assigned sequences is then 2.7×10−3 and the expected proportion of primer mismatched sequences should be 1.6×10−2.
Each smaller subset of sequences is then re-aligned and the saturation reassessed.
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PCR target sequences were then confirmed by Mayo Clinic's Advanced Genomic Technology Center DNA Sequencing Core.
The remaining sequences were then pooled with WGS scaffolds together to extend and collapse redundant sequences.
The left sequences were then used to do the following Bayesian evolutionary analysis.
Sequences were then dereplicated and sorted using the -derep_fulllength and -sortbysize commands.
A total of 30,443 such distinct sequences were then used to assemble a mtDNA sequence1.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com