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Both sequence sets contain one major cluster containing 86% and 52% of all sequences, respectively, and three smaller clusters of about 3 % and 5 in each set respectively.
In the NSI/SI dataset we obtained one major cluster containing 60% of all sequences, most of them of the NSI phenotype, and two smaller clusters each one containing 15% of all sequences, the first including solely NSI sequences, the second including equal percentage of sequences of both phenotypes.
Each library was assigned a major cluster containing genes specifically expressed in the particular tissue type or stress treatment of the library.
One major cluster containing six QTLs (qVA-1, qVA-2, qVA-3, qVA-4, qVA-5, and qVA-6) was detected between the narrow positions of 89.8 108.7 cM on LG6.
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The second major cluster contained all cancer spectra as well as one normal spectrum and another that is an obvious outlier within this group.
One difference is that the L. major cluster contains an U6 snRNA gene that is replaced by a tRNA-Gln gene in T. brucei.
However, only major clusters containing 50 or more genes are reported.
Five major clusters containing two or more closely linked NBS-LRR genes, which frequently showed low mutual sequence similarity, were identified from only a small sub-set (26) of mapped perennial ryegrass R genes.
From the zebrafish Zv3 and Zv4 assemblies, we found that 119 of the identified zebrafish OR genes are distributed in five major clusters containing between 14 and 31 genes each.
While only four STs contain both nasal carriage and clinical isolates, six of the major clusters contain both classes of isolates.
Hierarchical clustering analysis split the kidney biopsy samples into two major clusters, with one cluster containing four cancer tumor samples and one benign sample, and the other cluster containing five benign and two cancer tumor samples.
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Justyna Jupowicz-Kozak
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