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Fig. 1 | Genome Medicine

Fig. 1

From: Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populations

Fig. 1

Overall step-by-step workflow of the rapid whole sequencing (rWGS) protocol along with a timeline and data metrics/requirements at each step. Average data from 5 patients/families are displayed. Detailed data are available in the supplemental files, tables, and figures. Molecular findings in patients #2, #3, and #5 are also shown. SNVs, single nucleotide variants; INDELs, small insertions and deletions; SVs, structural variants including copy number variants and short tandem repeats

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