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Both clusters are in the intron of orthologous genes in the two species.
First, while the three QTL are presented as if they were the only traits in each cluster, in fact, both clusters are in genomic regions already known to be crowded with QTL.
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Given that both clusters are paramagnetic in IDS and diamagnetic in DTN, as well as the fact that the spectra of both clusters in IDS are broad, X may also be a large cluster with a structure similar to that of the P-cluster.
Both clusters are present in E. tasmaniensis and E. billingiae, but show variations in gene content (Additional file 4).
Our results for cluster 19.12 are summarized in Figure 1 and tabular results for both clusters are given in Additional file 1, including predicted domain content and genome positions of the putative chimpanzee genes.
Both NAT and SOHO clusters are in HA pairs and fully redundant, however, 15-45 secofds of intermittent connectivity to off-campus sites is possible.
Both clusters are also enriched in genes related to lipid biosynthetic process and for cluster 1, secondary metabolic and carbohydrate catabolic processes.
Logically, for the newly formed cluster, it assigns a value of "1" with another cluster only when all the units in both clusters are connected.
In the sense of this distance measure, two clusters are close when all subjects in both clusters are close.
Nevertheless, it is interesting to note that X has several spectral properties that are analogous to those of the P-cluster: (i) both clusters are paramagnetic with an integer spin in IDS; (ii) the spectra of both clusters in IDS are very broad, characteristic of large FeS clusters; and (iii) both clusters are diamagnetic in DTN.
Both clusters were identified in Korea in 2014, whereas members of the most evolved cluster were detected later in 2014 in Japan, Germany, the Netherlands, and the United Kingdom.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com