Reliability and performance of commercial RNA and DNA extraction kits for FFPE tissue cores

por Patel, Palak G., Selvarajah, Shamini, Guérard, Karl-Philippe, Bartlett, John M. S., Lapointe, Jacques, Berman, David M., Okello, John B. A., Park, Paul C.
Publicado 2017

Quantitative Assessment of the Sensitivity of Various Commercial Reverse Transcriptases Based on Armored HIV RNA

por Okello, John B. A., Rodriguez, Linda, Poinar, Debi, Bos, Kirsten, Okwi, Andrew L., Bimenya, Gabriel S., Sewankambo, Nelson K., Henry, Kenneth R., Kuch, Melanie, Poinar, Hendrik N.
Publicado 2010

Preparation of Formalin-fixed Paraffin-embedded Tissue Cores for both RNA and DNA Extraction

por Patel, Palak G., Selvarajah, Shamini, Boursalie, Suzanne, How, Nathan E., Ejdelman, Joshua, Guerard, Karl-Philippe, Bartlett, John M., Lapointe, Jacques, Park, Paul C., Okello, John B. A., Berman, David M.
Publicado 2016

GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretation

por Manshaei, Roozbeh, DeLong, Sean, Andric, Veronica, Joshi, Esha, Okello, John B. A., Dhir, Priya, Somerville, Cherith, Farncombe, Kirsten M., Kalbfleisch, Kelsey, Jobling, Rebekah K., Scherer, Stephen W., Kim, Raymond H., Hosseini, S. Mohsen
Publicado 2022

Assessment of the Implementation of Pharmacogenomic Testing in a Pediatric Tertiary Care Setting

por Cohn, Iris, Manshaei, Roozbeh, Liston, Eriskay, Okello, John B. A., Khan, Reem, Curtis, Meredith R., Krupski, Abby J., Jobling, Rebekah K., Kalbfleisch, Kelsey, Paton, Tara A., Reuter, Miriam S., Hayeems, Robin Z., Verstegen, Ruud H. J., Goldman, Aaron, Kim, Raymond H., Ito, Shinya
Publicado 2021

SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

por Ding, Qiliang, Somerville, Cherith, Manshaei, Roozbeh, Trost, Brett, Reuter, Miriam S., Kalbfleisch, Kelsey, Stanley, Kaitlin, Okello, John B. A., Hosseini, S. Mohsen, Liston, Eriskay, Curtis, Meredith, Zarrei, Mehdi, Higginbotham, Edward J., Chan, Ada J. S., Engchuan, Worrawat, Thiruvahindrapuram, Bhooma, Scherer, Stephen W., Kim, Raymond H., Jobling, Rebekah K.
Publicado 2022

The Cardiac Genome Clinic: implementing genome sequencing in pediatric heart disease

por Reuter, Miriam S., Chaturvedi, Rajiv R., Liston, Eriskay, Manshaei, Roozbeh, Aul, Ritu B., Bowdin, Sarah, Cohn, Iris, Curtis, Meredith, Dhir, Priya, Hayeems, Robin Z., Hosseini, S. Mohsen, Khan, Reem, Ly, Linh G., Marshall, Christian R., Mertens, Luc, Okello, John B. A., Pereira, Sergio L., Raajkumar, Akshaya, Seed, Mike, Thiruvahindrapuram, Bhooma, Scherer, Stephen W., Kim, Raymond H., Jobling, Rebekah K.
Publicado 2020

Genes and Pathways Implicated in Tetralogy of Fallot Revealed by Ultra-Rare Variant Burden Analysis in 231 Genome Sequences

por Manshaei, Roozbeh, Merico, Daniele, Reuter, Miriam S., Engchuan, Worrawat, Mojarad, Bahareh A., Chaturvedi, Rajiv, Heung, Tracy, Pellecchia, Giovanna, Zarrei, Mehdi, Nalpathamkalam, Thomas, Khan, Reem, Okello, John B. A., Liston, Eriskay, Curtis, Meredith, Yuen, Ryan K. C., Marshall, Christian R., Jobling, Rebekah K., Oechslin, Erwin, Wald, Rachel M., Silversides, Candice K., Scherer, Stephen W., Kim, Raymond H., Bassett, Anne S.
Publicado 2020