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Cluster 2 grouped 32 accessions and could be divided into two sub clusters: Subcluster 2 1 consisted of 15 accessions of garden pea accessions, spring field pea breeding and recombinant lines from a breeding program aiming at incorporating Aphanomyces euteiches resistance from garden pea resistance sources.
Type II genes were negatively modulated throughout the whole process and divided into four sub-clusters based on their expression level in three different processes.
The remaining cluster was roughly divided into four sub-clusters; two containing nearly all of the December crown bud samples and several November samples, with the remaining clusters made up of a mix of October and November crown bud samples.
The cluster I is further divided into two sub-clusters (I1, I2).
The first cluster (I) is divided into two sub-clusters (I1, I2).
The cluster V (J = 0.87) is divided into two sub-clusters.
The first one is further divided into two sub-clusters (Ia and Ib).
The non-OXLP cluster was divided into five sub-clusters, termed subclasses, which corresponded to their SWISS-PROT annotations (Fig. 1; as shown in Supplementary Table 2).
In[33], the two strongest clusters are divided into three sub-clusters: The first sub-cluster is composed of ten rays and has a zero delay offset, the second sub-cluster consists of six rays and has a delay offset of 5 ns and the last sub-cluster comprises four rays with a delay offset of 10 ns[33, p. 41].
The phylogenetic analyses of sxtA1 (Fig. 3; Supporting Information S1) show that all sxtA1 sequences formed one fully supported cluster, divided into two sub-clusters.
The procedure returned 2 main clusters of genes (in the first split of the data) associated with age (Figure 1), and each cluster could be further divided into two sub-clusters.
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