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In the last decade, multi gene methylation in breast primary tumors has been well-documented [ 6], but only small sets of genes have been shown to be methylated both in the primary tumor and in breast cancer metastasis.
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Only small sets of genes involved in proteolysis, peptidase activity and carbohydrates metabolism were still upregulated by pollen nutrition.
In general, only small sets of overlapping genes are shared between each pair of E-MAPs (e.g. of the 552 genes in the RNA E-MAP, only 125 are also present in the Chromosome E-MAP) yet the correlation between them is high (≥ 0.5, see Table 2) allowing inferences based on shared genes to be exploited by our method.
So the subsequent GSF have to investigate only small set of sequences, which likely to contain the true protein class.
Finally, we plotted the distribution of tags' reuse occurrences per number of tags (see Fig. 7), as well as the distribution of tags reuse occurrences per number of users (see Fig. 8). Figure 7 demonstrates a long-tail scheme, namely there are many tags which have been reused few times but only a small set of tags which have been reused many times.
Starting from the initially iodinated derivatives, a great variety of different compounds labeled with almost the whole set of available isotopes used in nuclear medicine tracer techniques have been described, but only a small set yet entered clinical trials.
Among dense arrays, m-sequences have perfect autocorrelation, but only small families, called maximal connected sets have good cross-correlation [4].
Since only small sample sets are available, small data analysis techniques are applied, and uncertainty levels are expected to be high.
A portion of the bivalent promoter set (either K4/K9 or K4/K27) from any single BTSC type was shared with fNSCs but there was only a small set of bivalent promoters that were shared among all BTSCs and fNSCs.
Multistage GWAS in addition to smaller association, linkage and candidate gene studies have led to the publication of thousands of variants, but only a relatively small set are likely to be truly related to breast cancer risk.
Among the tested BVMOs, only a small set of five BVMOs were shown to be active on ≥10 tested compounds, leaving only five potent BVMOs.
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CEO of Professional Science Editing for Scientists @ prosciediting.com