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However, once given access, it is straightforward to duplicate our analysis by following the steps enumerated in the methods section above.
Secondly, many analyses benefit from breaking down single error rates into two distinct classes of error allelic dropout and false alleles (Broquet and Petit, 2004)—which is not straightforward when both duplicates are error-prone.
Furthermore, separating redundant and non-redundant gene duplicates a priori is not straightforward.
Since networks can identify and blacklist duplicate IMEIs, this offers a relatively straightforward solution to the problem.
A straightforward explanation is that the sequence distance between duplicates (d) is determined by d = 2 vt, where v is the evolutionary rate of the protein sequence and t is the age of duplicates.
By generating all trees in canonical form, it is straightforward to test if two trees are isomorphic and prevent duplicate enumeration.
The method employed to distinguish authors by straightforward comparison of institution strings inevitably results in a large number of duplicates.
The most straightforward interpretation of the tree topology and the taxonomic distribution of genes is that NPAP1L duplicated in the lineage leading to primates, resulting in an NPAP1/UPF0607 gene.
While edge and node events are straightforward, node duplication/fusion events need more explanation because there are several different ways in which nodes can be duplicated or fused.
This is straightforward but broad analysis that aims to make some of the usual observations on the evolutionary properties of duplicated genes.
Too straightforward.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com