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Figure 2 | BMC Research Notes

Figure 2

From: Evaluation of SNP calling using single and multiple-sample calling algorithms by validation against array base genotyping and Mendelian inheritance

Figure 2

Pedigrees of the families with children affected with monogenic homozygous recessive disease. Star marked Individuals were not sequenced. Individuals in grey in the pedigrees had unknown phenotype. Individuals with no color are unaffected. Individuals in black color are affected with hypoplasia of cerebellum in A, and with abnormal pain sensation in B.

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