(A) Summary of high-throughput sequencing data sets on St. Jude Cloud. (B) Frequency of pediatric cancer types in WGS data generated from paired tumor-normal samples (left) or germline-only pediatric cancer survivors (right). (C) Genomic data contributed by RTCG deposition. Cumulative plot of WGS, WES and RNA-Seq released beginning May 2019 through July 2020 is shown at left while rare pediatric blood (n=13, 5 subtypes), solid (n=31, 16 subtypes) and germ cell (n=7, 6 subtypes) tumor samples uniquely represented in clinical genomics samples are shown at right.