Targeted long-read sequencing identifies missing disease-causing variation
Miller, D. E., Sulovari, A., Wang, T., Loucks, H., Hoekzema, K., Munson, K. M., Lewis, A. P., Fuerte, E. P. A., Paschal, C. R., Walsh, T., Thies, J., Bennett, J. T., Glass, I., Dipple, K. M., Patterson, K., Bonkowski, E. S., Nelson, Z., Squire, A., Sikes, M., … Eichler, E. E. (2021). Targeted long-read sequencing identifies missing disease-causing variation. The American Journal of Human Genetics, 108(8), 1436–1449. https://doi.org/10.1016/j.ajhg.2021.06.006
Grants:
R01HD100730
(NIH – Eunice Kennedy Shriver National Institute of Child Health & Human Development)
U54HD083091
(NIH – Eunice Kennedy Shriver National Institute of Child Health & Human Development)
R01EY029315
(NIH – National Eye Institute)
R01HL130996
(NIH – National Heart, Lung, and Blood Institute)
U24HG008956
(NIH – National Human Genome Research Institute)
R25HG007153
(NIH – National Human Genome Research Institute)
UM1HG006493
(NIH – National Human Genome Research Institute)
T32GM007088
(NIH – National Institute of General Medical Sciences)
T32GM007754
(NIH – National Institute of General Medical Sciences)
R01MH101221
(NIH – National Institute of Mental Health)
Publication Type:
Article
Unique ID:
10.1016/j.ajhg.2021.06.006
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Data Source:
Scopus
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