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A GBM tissue microarray was created with paraffin cores enriched for tumor cells as assessed by two independent neuropathologists.
A clone-based cDNA microarray was created by amplifying clone inserts from the most recent library used in the sequencing of the R. flavefaciens FD-1 genome to compare gene expression when R. flavefaciens FD-1 was grown on cellulose or cellobiose as a carbon and energy substrate.
A genomic microarray was created and used to characterise strains of Group II C. botulinum.
Briefly, a tissue microarray was created within the West of Scotland Pancreatic Unit, University Department of Surgery, Glasgow Royal Infirmary.
The human pancreatico-biliary tissue microarray was created within the West of Scotland Pancreatic Unit, University Department of Surgery, Glasgow Royal Infirmary.
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Incubation chambers corresponding to the size of the peptide microarray were created by using commercially available self-adhesive frames that are typically employed for the generation of incubation chambers for the hybridization of oligonucleotides (Fig. 1).
Correlation matrix for the 400 gene knockdown microarrays was created using Pearson correlation between individual knockdown datasets; an FDR cutoff of less than 0.05 was used.
Tissue microarrays were created for each histological subtype.
Triplicate cores were made of endometrial tumors pre- (endometrial biopsy) and postmetformin treatment (hysterectomy), and tissue microarrays were created.
To characterize the protein-DNA interaction profiles across different regions on the genome landscape, high-density microarrays are created and hybridization is used for the analysis of ChIP DNA (referred to as ChIP-on-chip).
Tissue microarrays were created from tissue samples from patients with GC who underwent gastrectomy and extended lymphadenectomy in 2005 and 2006 at the National Cancer Center in the Republic of Korea, as approved by the Institutional Review Board of the National Cancer Center in the Republic of Korea.
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