STRchive (pronouced S-T-archive) is the Short Tandem Repeat Archive. It is a database of STRs associated with rare diseases in humans.
STRs are a type of genetic variation that are associated with many rare diseases. Information about pathogenic STRs is often scattered across databases and out-of-date. This makes it difficult to find and interpret STR variants. STRchive aims to solve this problem by providing a central community database.
Hiatt, L., Weisburd, B., Dolzhenko, E., VanNoy, G.E., Kurtas, E.N., Rehm, H.L., Quinlan, A. and Dashnow, H., 2024. STRchive: a dynamic resource detailing population-level and locus-specific insights at tandem repeat disease loci. medRxiv doi: https://doi.org/10.1101/2024.05.21.24307682 .