High-Resolution Genomic Profiling of Chromosomal Abnormalities in Human Stem Cells Using the 135 K StemArray

por Elliott, Aaron M., Hohenstein Elliott, Kristi A., Kammesheidt, Anja
Publicado 2012

Not All Next Generation Sequencing Diagnostics are Created Equal: Understanding the Nuances of Solid Tumor Assay Design for Somatic Mutation Detection

por Gray, Phillip N., Dunlop, Charles L.M., Elliott, Aaron M.
Publicado 2015

Mutations in RASA1 and GDF2 identified in patients with clinical features of hereditary hemorrhagic telangiectasia

por Hernandez, Felicia, Huether, Robert, Carter, Lester, Johnston, Tami, Thompson, Jennifer, Gossage, James R, Chao, Elizabeth, Elliott, Aaron M
Publicado 2015

Cold Preflush of Porcine Kidney Grafts Prior to Normothermic Machine Perfusion Aggravates Ischemia Reperfusion Injury

por Fabry, Gregor, Doorschodt, Benedict M., Grzanna, Tim, Boor, Peter, Elliott, Aaron, Stollenwerk, André, Tolba, René H., Rossaint, Rolf, Bleilevens, Christian
Publicado 2019

The Validation and Clinical Implementation of BRCAplus: A Comprehensive High-Risk Breast Cancer Diagnostic Assay

por Chong, Hansook Kim, Wang, Tao, Lu, Hsiao-Mei, Seidler, Sara, Lu, Hong, Keiles, Steven, Chao, Elizabeth C., Stuenkel, A. J., Li, Xiang, Elliott, Aaron M.
Publicado 2014

A Bayesian framework for efficient and accurate variant prediction

por Qian, Dajun, Li, Shuwei, Tian, Yuan, Clifford, Jacob W., Sarver, Brice A. J., Pesaran, Tina, Gau, Chia-Ling, Elliott, Aaron M., Lu, Hsiao-Mei, Black, Mary Helen
Publicado 2018

Detection of structural variation using target captured next-generation sequencing data for genetic diagnostic testing

por Mu, Wenbo, Li, Bing, Wu, Sitao, Chen, Jefferey, Sain, Divya, Xu, Dong, Black, Mary Helen, Karam, Rachid, Gillespie, Katrina, Farwell Hagman, Kelly D., Guidugli, Lucia, Pronold, Melissa, Elliott, Aaron, Lu, Hsiao-Mei
Publicado 2018

DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes

por Richardson, Marcy E., Chong, Hansook, Mu, Wenbo, Conner, Blair R., Hsuan, Vickie, Willett, Sara, Lam, Stephanie, Tsai, Pei, Pesaran, Tina, Chamberlin, Adam C., Park, Min-Sun, Gray, Phillip, Karam, Rachid, Elliott, Aaron
Publicado 2018

Correction: DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes

por Richardson, Marcy E., Chong, Hansook, Mu, Wenbo, Conner, Blair R., Hsuan, Vickie, Willett, Sara, Lam, Stephanie, Tsai, Pei, Pesaran, Tina, Chamberlin, Adam C., Park, Min-Sun, Gray, Phillip, Karam, Rachid, Elliott, Aaron
Publicado 2018

Evidence of two deeply divergent co-existing mitochondrial genomes in the Tuatara reveals an extremely complex genomic organization

por Macey, J. Robert, Pabinger, Stephan, Barbieri, Charles G., Buring, Ella S., Gonzalez, Vanessa L., Mulcahy, Daniel G., DeMeo, Dustin P., Urban, Lara, Hime, Paul M., Prost, Stefan, Elliott, Aaron N., Gemmell, Neil J.
Publicado 2021

An evaluation of GPUs for use in an upgraded ATLAS High Level Trigger

por Tavares Delgado, Ademar, Conde Mui\~no, Patricia, Bold, Tomasz, Augusto, Jose, Kama, Sami, Negrini, Matteo, Sidoti, Antonio, Rinaldi, Lorenzo, Tupputi, Salvatore, Baines, John, Bauce, Matteo, Messina, Andrea, Emeliyanov, Dmitry, Elliott, Aaron Kyle, Greenwood, Zeno Dixon, Laosooksathit, Supada
Publicado 2015

Quantitative Analysis of BRCA1 and BRCA2 Germline Splicing Variants Using a Novel RNA-Massively Parallel Sequencing Assay

por Farber-Katz, Suzette, Hsuan, Vickie, Wu, Sitao, Landrith, Tyler, Vuong, Huy, Xu, Dong, Li, Bing, Hoo, Jayne, Lam, Stephanie, Nashed, Sarah, Toppmeyer, Deborah, Gray, Phillip, Haynes, Ginger, Lu, Hsiao-Mei, Elliott, Aaron, Tippin Davis, Brigette, Karam, Rachid
Publicado 2018

An evaluation of GPUs for use in an upgraded ATLAS High Level Trigger

por Tavares Delgado, Ademar, Bold, Tomasz, Pastore, Francesca, Conde Muino, Patricia, Augusto, Jose, Kama, Sami, Negrini, Matteo, Sidoti, Antonio, Rinaldi, Lorenzo, Tupputi, Salvatore, Baines, John, Bauce, Matteo, Messina, Andrea, Emeliyanov, Dmitry, Elliott, Aaron Kyle, Greenwood Jr, Dick, Laosooksathit, Supada
Publicado 2015

Somatic TP53 variants frequently confound germline testing results

por Weitzel, Jeffrey N., Chao, Elizabeth C., Nehoray, Bita, Van Tongeren, Lily R., LaDuca, Holly, Blazer, Kathleen R., Slavin, Thomas, Pesaran, Tina, Rybak, Christina, Solomon, Ilana, Niell-Swiller, Mariana, Dolinsky, Jill S., Castillo, Danielle, Elliott, Aaron, Gau, Chia-Ling, Speare, Virginia, Jasperson, Kory
Publicado 2017

TumorNext: A comprehensive tumor profiling assay that incorporates high resolution copy number analysis and germline status to improve testing accuracy

por Gray, Phillip N., Vuong, Huy, Tsai, Pei, Lu, Hsaio-Mei, Mu, Wenbo, Hsuan, Vickie, Hoo, Jayne, Shah, Swati, Uyeda, Lisa, Fox, Susanne, Patel, Harshil, Janicek, Mike, Brown, Sandra, Dobrea, Lavinia, Wagman, Lawrence, Plimack, Elizabeth, Mehra, Ranee, Golemis, Erica A., Bilusic, Marijo, Zibelman, Matthew, Elliott, Aaron
Publicado 2016

Mutational and splicing landscape in a cohort of 43,000 patients tested for hereditary cancer

por Horton, Carolyn, Cass, Ashley, Conner, Blair R., Hoang, Lily, Zimmermann, Heather, Abualkheir, Nelly, Burks, David, Qian, Dajun, Molparia, Bhuvan, Vuong, Huy, LaDuca, Holly, Grzybowski, Jessica, Durda, Kate, Pilarski, Robert, Profato, Jessica, Clayback, Katherine, Mahoney, Martin, Schroeder, Courtney, Torres-Martinez, Wilfredo, Elliott, Aaron, Chao, Elizabeth C., Karam, Rachid
Publicado 2022

Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer

por Karam, Rachid, Conner, Blair, LaDuca, Holly, McGoldrick, Kelly, Krempely, Kate, Richardson, Marcy E., Zimmermann, Heather, Gutierrez, Stephanie, Reineke, Patrick, Hoang, Lily, Allen, Kyle, Yussuf, Amal, Farber-Katz, Suzette, Rana, Huma Q., Culver, Samantha, Lee, John, Nashed, Sarah, Toppmeyer, Deborah, Collins, Debra, Haynes, Ginger, Pesaran, Tina, Dolinsky, Jill S., Tippin Davis, Brigette, Elliott, Aaron, Chao, Elizabeth
Publicado 2019

TumorNext-Lynch-MMR: a comprehensive next generation sequencing assay for the detection of germline and somatic mutations in genes associated with mismatch repair deficiency and Ly...

por Gray, Phillip N., Tsai, Pei, Chen, Daniel, Wu, Sitao, Hoo, Jayne, Mu, Wenbo, Li, Bing, Vuong, Huy, Lu, Hsiao-Mei, Batth, Navanjot, Willett, Sara, Uyeda, Lisa, Shah, Swati, Gau, Chia-Ling, Umali, Monalyn, Espenschied, Carin, Janicek, Mike, Brown, Sandra, Margileth, David, Dobrea, Lavinia, Wagman, Lawrence, Rana, Huma, Hall, Michael J., Ross, Theodora, Terdiman, Jonathan, Cullinane, Carey, Ries, Savita, Totten, Ellen, Elliott, Aaron M.
Publicado 2018

Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes

por Landrith, Tyler, Li, Bing, Cass, Ashley A., Conner, Blair R., LaDuca, Holly, McKenna, Danielle B., Maxwell, Kara N., Domchek, Susan, Morman, Nichole A., Heinlen, Christopher, Wham, Deborah, Koptiuch, Cathryn, Vagher, Jennie, Rivera, Ragene, Bunnell, Ann, Patel, Gayle, Geurts, Jennifer L., Depas, Morgan M., Gaonkar, Shraddha, Pirzadeh-Miller, Sara, Krukenberg, Rebekah, Seidel, Meredith, Pilarski, Robert, Farmer, Meagan, Pyrtel, Khateriaa, Milliron, Kara, Lee, John, Hoodfar, Elizabeth, Nathan, Deepika, Ganzak, Amanda C., Wu, Sitao, Vuong, Huy, Xu, Dong, Arulmoli, Aarani, Parra, Melissa, Hoang, Lily, Molparia, Bhuvan, Fennessy, Michele, Fox, Susanne, Charpentier, Sinead, Burdette, Julia, Pesaran, Tina, Profato, Jessica, Smith, Brandon, Haynes, Ginger, Dalton, Emily, Crandall, Joy Rae-Radecki, Baxter, Ruth, Lu, Hsiao-Mei, Tippin-Davis, Brigette, Elliott, Aaron, Chao, Elizabeth, Karam, Rachid
Publicado 2020