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RGTV: VanBrocklin family find answers with WGS provided by iHope Program

The VanBrocklin's, a family from Wisconsin, received free clinical whole genome sequencing through Rare Genomics as part of its iHope program in collaboration with Illumina, Inc. Through this test, both children received answers in their diagnostic journey. It is our hope that more support is given for undiagnosed children, so that they may receive the treatments and care that they have desperately needed throughout the years.

RG is an international non-profit that provides access to cutting edge research technologies, physicians, and scientists across the globe. By providing an expert network, RG helps families pursue personalized research projects in diseases not otherwise studied.