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In all, the LC dataset accounts for 34 of the 72 proteins and 44 interactions (Fig. 3 and Table 1) and displays some overlap with the HT-Y2H [1]–[3] and PCA studies [4].
The PCA dataset accounts for 25 of the 72 SSU processome proteins and 27 interactions among them — the highest coverage among the genome-wide studies (Fig. 2 and Table 1) and shows some overlap of PPIs with the Uetz et al. [1] dataset.
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In contrast, only one PSF was identified in genomic methylation dataset accounting for 0.2% of total variance.
Three population stratification factors (PSFs) were identified in the genomic SNP dataset, accounting for a relatively large portion of total variance (6%).
The first three components extracted from the dataset accounted for 79.4% of the morphological variation.
We found 30 CNVRs that overlapped with CNVRs in that dataset, accounting for 61.22% of their CNV calls.
For example, 5 out the 26 anthroposophic GPs in the dataset account for more than 95% of the claims by patients with anthroposophic GP.
Interestingly, miR156 is the second most abundant miRNA in the barley dataset, accounting for about 3.7% of the total reads (Additional file 1).
Among the dinucleotide repeats (DNRs), AG/CT repeats (6,034) were the most common in the dataset, accounting for 76% of the total DNRs (7,942) (Table 2).
Among the dinucleotide repeat motifs identified, AG/CT repeats (1350) were the most common in the dataset, accounting for 69.6% of the total dinucleotide motifs (1939).
The two-dimensional PCoA for 230 individuals in 13 populations based on ISSR dataset accounted for 28.15 % (axis 1) and 18.43 % (axis 2) of total variance, respectively [see Supporting Information— Fig. S7 ].
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