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. 2021 Feb 15;372:n214. doi: 10.1136/bmj.n214

Fig 1.

Fig 1

Explanation of genotyping using SNP chip technology. Example cluster plots for common variant (top) and rare variant (bottom). Each circle represents one person’s DNA assayed at specific position on SNP chip when known variant (G to C) exists. Automated clustering across multiple individuals is used to determine which DNA base is present in each person at that position. Pink circles in main cluster represent most common reference base (G), orange circles represent heterozygous variant (C), and pale purple circles represent uncertain or missing results due to experimental noise