Sentence examples for between different tumor samples from inspiring English sources

Taken together, the somatic mutation spectrum showed very high heterogeneity in ESCC between different tumor samples.

The differences in the interferon and signal transducer and activator of transcription 1 (STAT1) metagenes are smaller than those observed between different tumor samples, which might suggest considerable expression of those interferon-induced genes by the carcinoma and/or stromal cells of the tumor.

This ratio could also indicate the correlation between cancer cell lines and different tumor samples, as it shows high consistency with that only by copy number profiles or gene expression profiles.

Therefore, instead of searching for classification patterns between tumor samples based on gene expression profiles we used a reverse engineering approach in order to search for common patterns among different tumor samples.

For 10 RCC cases, we observed different VHL genotypes in different tumor samples obtained from one tumor.

We also assume that different tumor samples have different mutation rates.

While the relative small sample sizes (n = 8~9) of the different BRCA1-defined groups examined here may contributes to the paucity of consistent differences identified, it does represent the largest series examined to date and a larger number of differentially expressed genes can usually be identified between different tumor types with similar sample sizes [ 31, 32].

Table 1 summarizes the results obtained from the immunohistochemistry of the breast lesions and illustrates the difference in staining percentage (positive cases out of the total number of samples studied) between different tumor types, implying differential incidence of GIPC1 enhanced expression.

In other cases, authors developed signatures of differentially expressed genes that allow distinguishing between different tumor stages [ 27, 28], or normal samples from tumors and metastases [ 29- 31].

Vascular permeability is highly variable between different tumor types, among patients with the same type of tumor, and between distinct tumors within an individual subject.

In this fashion, probe sets with high b/w scores showed greater variation between different primary tumors than between treatment paired tumor samples, whereas genes with low b/w scores showed greater variation within treatment paired tumors samples than between different tumors.