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. 2020 Jun 8;15:144. doi: 10.1186/s13023-020-01420-w

Fig. 2.

Fig. 2

Example of filtering of genomic variants obtained by whole exome sequencing to identify a pathogenic variant in a growth retarded patientn. By applying different filter parameters like variant frequencies, pathogenicity and mode of inheritance, the number of genomic variants can be reduced and the disease-causing variant can be identified (numbers of variants are shown on the y axis)