C
Camille B. Troup
Researcher at Bio-Rad Laboratories
Publications - 7
Citations - 2274
Camille B. Troup is an academic researcher from Bio-Rad Laboratories. The author has contributed to research in topics: TaqMan & Antibody. The author has an hindex of 2, co-authored 5 publications receiving 1918 citations.
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Journal ArticleDOI
High-Throughput Droplet Digital PCR System for Absolute Quantitation of DNA Copy Number
Benjamin J. Hindson,Kevin D. Ness,Donald A. Masquelier,Phillip Belgrader,Nicholas J. Heredia,Anthony J. Makarewicz,Isaac J. Bright,Michael Y. Lucero,Amy L. Hiddessen,Tina C. Legler,Tyler K. Kitano,Michael R. Hodel,Jonathan Petersen,Paul Wyatt,Erin R. Steenblock,Pallavi Shah,Luc J. Bousse,Camille B. Troup,Jeffrey Clark Mellen,Dean K. Wittmann,Nicholas G. Erndt,Thomas H. Cauley,Ryan T. Koehler,Austin P. So,Simant Dube,Klint Rose,Luz Montesclaros,Shenglong Wang,David P. Stumbo,Shawn Hodges,Steven Romine,Fred P. Milanovich,Helen E. White,John F. Regan,George Karlin-Neumann,Christopher Hindson,Serge Saxonov,Bill W. Colston +37 more
TL;DR: A high-throughput droplet digital PCR system that enables processing of ∼2 million PCR reactions using conventional TaqMan assays with a 96-well plate workflow is described that will allow researchers to explore complex genetic landscapes, discover and validate new disease associations, and define a new era of molecular diagnostics.
Journal ArticleDOI
Subclonal mutations in SETBP1 confer a poor prognosis in juvenile myelomonocytic leukemia
Elliot Stieglitz,Camille B. Troup,Laura C. Gelston,John R. Haliburton,Eric D. Chow,Kristie B. Yu,Jon Akutagawa,Amaro Taylor-Weiner,Y. Lucy Liu,Yong-Dong Wang,Kyle Beckman,Peter D. Emanuel,Benjamin S. Braun,Adam R. Abate,Robert B. Gerbing,Todd A. Alonzo,Mignon L. Loh +16 more
TL;DR: Using droplet digital polymerase chain reaction, SETBP1 mutations were identified in 17/56 of patients who were treated in the Children's Oncology Group sponsored clinical trial, AAML0122, and five-year event-free survival in patients with SET BP1 mutations was 18% ± 9% compared with 51% ± 8% for those without mutations.
Journal ArticleDOI
Bivalent intra-spike binding provides durability against emergent Omicron lineages: Results from a global consortium
Heather M. Callaway,Kathryn M. Hastie,Sharon L. Schendel,Haoyang Li,Xiaoying Yu,Jeremy Shek,Tierra Buck,Sean Hui,Daniel Bedinger,Camille B. Troup,S. Moses Dennison,Kan Li,Michael D. Alpert,Charles C. Bailey,Sharon Benzeno,Jody Bonnevier,Jin-Qiu Chen,Charm Chen,Hyeseon Cho,Peter D. Crompton,Vincent Dussupt,Kevin C. Entzminger,Yassine Ezzyat,Jonathan K. Fleming,Nick Geukens,Amy E. Gilbert,Yongjun Guan,Xiaojian Han,Christopher D. Harvey,Julia M. Hatler,Bryan Howie,Chaoying Hu,Ailong Huang,Maya Imbrechts,Aishun Jin,Nik Kamachi,Gladys J. Keitany,Mark Klinger,Jay K. Kolls,Shelly J. Krebs,Tingting Li,Feiyang Luo,T. Maruyama,Michael Meehl,Letzibeth Mendez-Rivera,Andrea Musa,C.J. Okumura,Benjamin E. R. Rubin,Aaron K. Sato,Meiying Shen,Anirudh K. Singh,Shuyi Song,Joshua Hoong Yu Tan,Jeffrey M. Trimarchi,Dhruvkumar Upadhyay,Yingming Wang,Lei Yu,Tom Z. Yuan,Erik Yusko,Bjoern Peters,Georgia D. Tomaras,Erica Ollmann Saphire +61 more
TL;DR: The SARS-CoV-2 Omicron variant of concern (VoC) and its sublineages contain 31-36 mutations in spike and escape neutralization by most therapeutic antibodies as mentioned in this paper .
Proceedings ArticleDOI
Abstract 4859: Ultra-sensitive detection of rare mutants by droplet digital PCR with conventional TaqMan assays
Benjamin J. Hindson,Austin P. So,Ryan T. Koehler,Camille B. Troup,Nicholas J. Heredia,George Karlin-Neumann,Serge Saxonov,Helen E. White +7 more
TL;DR: Results on the use of ddPCR for the detection and quantitation of several clinically important mutations, including KRAS, c-KIT D816V and JAK2 from clinical samples such as bone marrow aspirates and FFPE are presented.
Journal ArticleDOI
Subclonal Mutations in SETBP1 Predict Relapse in Juvenile Myelomonocytic Leukemia
Elliot Stieglitz,Camille B. Troup,Laura C. Gelston,Eric D. Chow,Kristie B. Yu,Jon Akutagawa,Amaro Taylor-Weiner,Y. Lucy Liu,Peter D. Emanuel,Benjamin S. Braun,Robert B. Gerbing,Todd A. Alonzo,Mignon L. Loh +12 more
TL;DR: It is concluded that the presence of a subclonal mutation in SETBP1 is a novel biomarker of adverse outcome in JMML, and the hypothesis that rare SETBP 1 mutant clones exist at diagnosis in many patients who relapse, and that these rare cells undergo positive selection during treatment is tested.