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The platforms are shown to be enable efficient for selective adsorption of a variety of bio-substances including protein arrays, latex beads, and single cells.
In addition, differences of the thermal comfort conditions on the platforms are shown to be associated with the depth and the design characteristics of the stations.
Through analyzing Affymetrix and Agilent 44K anatomic meta-profiles, 19 root-preferential genes were identified and their anatomic (Figure2a and2c; Electronic Additional file2: Figure S1a and c) and developmental expression patterns (Figure2b; Electronic Additional file2: Figure S1b, d and e) on both platforms are shown in Figure2 and electronic Additional file2: Figure S1.
Only HSCT donors of the discovery cohort that were profiled on both assay platforms are shown.
Venn diagrams of the SNP calls shared among the three platforms are shown in Figure 1.
The top 50 discriminator genes over all four microarray platforms are shown in Figure 3 (complete list is given as Additional file 9).
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As the landscape evolves, new digital platforms are showing their potential to make learning more engaging and personalized and to improve assessment and collaboration.
A comparison between temperature time series recorded at different platforms is shown.
The channel utilization under different platforms is shown in Table 3.
Comparison of peak sets identified using ChIP-chip and ChIP-seq for H3K9me3, SETDB1, and KAP1 and a comparison of the binding patterns for H3K9me3, SETDB1, and KAP1 using the different platforms is shown in Supplementary Figure S6.
CTC-based platforms were shown to be effective for testing the efficacy of novel drugs.
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