Sentence examples for subclass supplementary from inspiring English sources

IgG N-glycome of distinct subclasses (IgG1, IgG2/3, and IgG4) was analysed by LC-ESI-MS and resulted in 20 glycoforms and 7 derived traits per subclass (Supplementary Table 2).

Even when unsupervised hierarchical clustering was performed separately, based not on signal ratios but on the presence or absence of DNA hypomethylation and the presence or absence of DNA hypermethylation, the majority of patients in Cluster BN were clustered into the same subclass (supplementary Figure S1A and B is available at Carcinogenesis Online).

Even when unsupervised hierarchical clustering was performed separately, based not on signal ratios but on the presence or absence of DNA hypomethylation and the presence or absence of DNA hypermethylation, the majority of patients in Cluster BT were clustered into the same subclass (supplementary Figure S1C and D is available at Carcinogenesis Online).

More than half of the NBS-LRR subclasses in each Solanaceae genome were classified into 37 subclasses (Supplementary Table 41).

As demonstrated by cross-species similarities in relative expression ratio of orthologous genes between subclasses (Supplementary Figs. 4 and 5 online) and measurable phenotypes (Fig. 3), mimicry of the mouse models of subclasses of human HCC may, to a large extent, be due to the similarity in the underlying biology of the disease.

This database compiles composition data on lignans and the six flavonoid subclasses (Supplementary Table 1).

Alignment of complete Alu sequences showed that the 22-nucleotide hotspot sequence is conserved among all Alu subclasses (Supplementary Material, Fig. S2).

In this work, we analyzed a subset of 74 lipoprotein subclass measures (Supplementary Table S3).

Cervical and vaginal anomalies are classified in independent supplementary subclasses.  .

Following this approach, a 1.4 ml polyclonal anti-KLH stock was obtained in which all major immunoglobulin isotypes and IgG subclasses were represented (Supplementary Table 1, available online).

Our analysis also shows that the larger amounts of repetitive DNA in C. brenneri and C. remanei compared with C. elegans and in D. virilis compared with D. melanogaster do not result simply from elevated copy number in one or a few TE families but rather from an increase in the number of TE families in almost all subclasses (table 1; supplementary figs. 1 and 2, Supplementary Material online).