Samuel Angiuoli
Affiliations: | 2011 | Computer Sciene | University of Maryland, College Park, College Park, MD |
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Publications
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| Keefer LA, White JR, Wood DE, et al. (2022) Automated next-generation profiling of genomic alterations in human cancers. Nature Communications. 13: 2830 |
| Lee Deak K, Jackson JB, Valkenburg KC, et al. (2021) Next-Generation Sequencing Concordance Analysis of Comprehensive Solid Tumor Profiling between a Centralized Specialty Laboratory and the Decentralized PGDx Elio Tissue Complete Kitted solution. The Journal of Molecular Diagnostics : Jmd |
| Georgiadis A, Durham JN, Keefer LA, et al. (2019) Noninvasive Detection of Microsatellite Instability and High Tumor Mutation Burden in Cancer Patients Treated with PD-1 Blockade. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research |
| Chowbina S, Cerqueira G, Sweeney D, et al. (2019) Abstract 1665: Development of standardized assay and software systems to deliver concordant results across sequencing platforms Cancer Research. 79: 1665-1665 |
| Gerding KMR, Valkenburg KC, Oliveras C, et al. (2019) Abstract B027: Analytical validation of a 500+ gene comprehensive NGS assay to detect genomic alterations across 35 tumor types Molecular Cancer Therapeutics. 18 |
| Wood DE, White JR, Georgiadis A, et al. (2018) A machine learning approach for somatic mutation discovery. Science Translational Medicine. 10 |
| Wood D, White J, Georgiadis A, et al. (2018) Abstract 3271: A machine learning approach for somatic mutation discovery Cancer Research. 78: 3271-3271 |
| Nesselbush M, Jones S, Keefer L, et al. (2018) Abstract A027: Analytic validation of a pan-cancer tumor mutational burden assay Molecular Cancer Therapeutics. 17 |
| Phallen J, Sausen M, Adleff V, et al. (2017) Direct detection of early-stage cancers using circulating tumor DNA. Science Translational Medicine. 9 |
| Agrawal S, Arze C, Adkins RS, et al. (2017) CloVR-Comparative: automated, cloud-enabled comparative microbial genome sequence analysis pipeline. Bmc Genomics. 18: 332 |