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Kalyn M. Hubbard

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Articles

A blended genome and exome sequencing method captures genetic variation in an unbiased and cost-effective manner

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By Toni Boltz, Benjamin Chu, Matthew DeFelice, Calwing Liao, Julia M. Sealock, Robert Ye, Lerato Majara, Jack M. Fu, Lingyu Zhan, Sarah E. Medland, Sinéad B. Chapman, Simone Rubinacci, Jonna Grimsby, Tamrat Abebe, Melkam Alemayehu, Elizabeth Atkinson Verified, Tim B. Bigdeli, Harrison A. Brand, Lori B. Chibnik, Samuel Deluca, Ana M Diaz-Zuluaga, Abebaw Fekadu, Michael Gatzen, Bizu Gelaye, Toni Hill, Hailiang Huang, Roxanne James, Moses Joloba, Christopher Kachulis, Rogers Kamulegeya, Gabriel Kigen, Soyeon Kim, Nastassja Koen, Edith Kwobah, Seungmo Lee, Niall J Lennon, Penelope A. Lind, Esteban Lopera-Maya, Johnstone Makale, Serghei Mangul, Justin McMahon, Noeline Nakasujja, Carter Newman, Lethukuthula L. Nkambule, Ana Olivares, Catherine M Olsen, Linnet Ongeri, Sophie Parsa, Shengying Qin, Raj Ramesar, Chiara Sabatti, Jacquelyn Schneider, Christine Stevens, Anne Stevenson, Erik Stricker, Jessie Tang, Megan Townsend Verified, David Whiteman, Mary T. Yohannes, Mingrui Yu, Kai Yuan, NeuroGap-Psychosis Study, Dickens Akena, Lukoye Atwoli, Symon M Kariuki, Karestan C. Koenen, Charles Newton, Dan Stein, Solomon Teferra, Zukiswa Zingela, Carlos N. Pato, Michele Pato, Carlos Lopez-Jaramillo, Nelson B. Freimer, Roel A. Ophoff, Loes M. Olde Loohuis, Michael E. Talkowski, Benjamin M. Neale, Daniel P. Howrigan, Alicia Martin, Jacqueline I. Goldstein, Fred K. Ashaba, Amanda B. Bradway, Stella Gichuru, Marissa L. Gildea, Kalyn M. Hubbard, Wilfred E. Injera, Phillip R. Kalmbach, Joseph Kyebuzibwa, Pierre Mowlem, Henry Musinguzi, Rehema M. Mwema, Conor R. O’Neil, Adele Pretorius, Faye L. Reagan, Welelta Shiferaw, Rocky E. Stroud II
| Nature Verified
Abstract Here we developed and deployed the blended genome exome (BGE) method, a DNA library approach that generates low-pass whole-genome (1–4× mean depth) and deep whole-exome (30–40× mean depth) data in a single sequencing run. BGE is cost-effective, empowers most genomic discoveries possible with deep whole-genome sequencing and captures global common single-nucleotide polymorphism diversity.
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