Pais, L. S., Snow, H., Weisburd, B., Zhang, S., Baxter, S. M., DiTroia, S., O'Heir, E., England, E., Chao, K. R., Lemire, G., Osei‐Owusu, I., VanNoy, G. E., Wilson, M., Nguyen, K., Arachchi, H., Phu, W., Solomonson, M., Mano, S., O'Leary, M., Lovgren, A., Babb, L., Austin‐Tse, C. A., Rehm, H. L., MacArthur, D. G., & O'Donnell‐Luria, A. (2022). seqr: A web‐based analysis and collaboration tool for rare disease genomics. Human mutation, 43(6), 698–707. http://access.bl.uk/ark:/81055/vdc_100155165817.0x000016