A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families

Revital Bronstein(Massachusetts Eye and Ear Infirmary), Eric A. Pierce(Broad Institute), Alex D. Jansen(University of Wisconsin–Madison), Mathew Maher(Massachusetts Eye and Ear Infirmary), Daniel Navarro-Gomez, David M. Gamm(McPherson College), Emily Place(MACOM (United States)), Elizabeth E. Capowski(University of Wisconsin–Madison), Kinga M. Bujakowska(Massachusetts Eye and Ear Infirmary), Sudeep Mehrotra(Massachusetts Eye and Ear Infirmary), Riccardo Sangermano(Radboud University Nijmegen)
Human Molecular Genetics
January 21, 2020
Cited by 24


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