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To obtain these diagrams we divide the LASCO images of a given sequence in angular slices, transform them into rectangular slices (their width chosen proportional to the time distance to the next image) and place them side by side.
Let be a given sequence in such that (7.12).
Recall (see [52, 53]) that if is a given sequence in, is defined recurrently by and for.
Let ((X, d)) be a metric space and ({x_{n}}) a given sequence in X. Suppose that lim_{n to+infty} d(x_{n}, x_{n+1}) = 0.
Let { λ n } be a given sequence in ( 0, 1 ) such that ∑ n = 1 ∞ λ n = 1, let { v n } be a bounded sequence in X, and let v 0 be an arbitrary point in X.
These techniques are still commonly encountered in studies whose primary focus is not tephrochronology, but where such an identification still serves the purpose of anchoring a given sequence in time (e.g. pedological and palynological investigations, e.g. [63 66]).
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This gives almost constant access to any coordinate in a given sequence i.e. chromosome.
Unlike genomes where most sequences should be approximately equally represented, coverage of any given sequence in a transcriptome can vary over several orders of magnitude due to expression differences [ 4].
An artificial gene is the DNA strand of a given sequence, synthesized in vitro.
Mass spectrometry is highly sensitive and can detect small amounts of a nucleic acid of a given sequence even in a complex mixture.
Since for a given sequence context in SMRT sequencing, the kinetic signatures of 5mC, 5hmC, 5fC, and 5caC are different, there is the potential for direct identification of the various modifications on native DNA samples.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com