Skip to main content
Fig. 4 | BMC Cancer

Fig. 4

From: Precision oncology using a limited number of cells: optimization of whole genome amplification products for sequencing applications

Fig. 4

Point mutation detection and aCGH analysis using a single-cell WGA products that passed (QC-pass) or failed (QC-fail) the quality control step, b) 5 and 10-cell WGA products with passing QC, and c unamplified, batch genomic DNA. Single-cell WGA products (QC-fail vs. QC-pass) exhibit significantly different downstream analyses results despite using cells isolated from a clonally expanded cell line. The single-cell WGA product with the passing QC (QC-pass) generated Sanger sequencing and aCGH results that more closely resembled that of the unamplified batch gDNA compared to the single-cell WGA product failing the QC (QC-fail). Red arrows signify the areas of alteration that were detected in QC-pass and batch gDNA, but not in QC-fail. d aCGH quality metrics (DLRS and signal-to-noise ratio) for 1, 5 and 10-cell WGA products and batch gDNA. Improved DLRS values were associated with WGA products that passed the QC step as well as using an increasing number of starting cellular input

Back to article page