Sentence examples for cluster assays from inspiring English sources

Tandem GC cluster assays were defined as GC-rich regions that overlapped with at least two classified clusters.

All the proteins of the yeast peroxisome network are listed in Additional file 1, while the PPI network is shown in Additional file 2. The network consists of 450 proteins (61 core and 389 neighbor proteins) and 2,433 PPI (128 core-core, 501 core-neighbor and 1,804 neighbor-neighbor PPI), which have been detected by binary or cluster assays (Table 1).

This interaction was found using non-biased Fc-IL1RAPL1 affinity chromatography and mass-spectrometry analysis using brain extract and then confirmed by HEK cell trans-clustering assays and immunoprecipitation by trans-interaction.

From the 137 clusters assayed, we reconstructed 71 dam genotypes, 18 of which matched the genotypes of collected females (with probability of genetic identity ranging from 10−14 to 10−8; Table S 1).

As negative control, we performed cell cluster assay by dissolving buffers (Fig. S9).

The method was described in the section "cell cluster assay" and used dissolving buffers, PBS (Fig. S9a; control for Fig. 1a,b), TD (Fig. S9b. control for Fig. 1c) were used.

We therefore studied the three-dimensional growth capacity of MDA-MB 231 derived cells with the Matrigel cluster assay (Figure 2c).

The biological functions of the Large-induced functional glycans on α-DG in these cells were further supported by their cell surface localization examined by immuno-fluorescent microscopy with the IIH6 antibody (Fig. 1B) and the laminin cluster assay (Fig. 1C).

Despite the presence of an intact gene cluster, pyoverdine assays indicated that PAHM4 produces minimal pyoverdine (data not shown).

Tag SNPs that failed manufacturing (ordered but did not convert), failed validation (no amplification or clustering) and assays that had less than 80% completion or 80% concordance with the 90 Hapmap CEU samples used for validation were excluded (n = 104).

These findings demonstrate a structural basis to clustering of assays in the chemical similarity matrix.