Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Charles Elfe"'
Autor:
Charles Elfe, Cynthia L. Hendrickson, Theodore B. Davis, Amy B. Emerman, Fiona A. Stewart, Kruti M. Patel, Eileen T. Dimalanta, Salvatore Russello, Sarah K. Bowman, Scott M. Adams, Andrew Barry, Evan Mauceli
Publikováno v:
Cancer Research. 78:3416-3416
Efficient utilization of targeted gene panels for clinical research is challenged by the wide variation in gene constituents specific to a given study. While focused gene panels efficiently provide the necessary depth of coverage for low-frequency va
Autor:
Sarah K. Bowman, Cynthia L. Hendrickson, Scott M. Adams, Theodore B. Davis, Andrew Barry, Charles Elfe, Evan Mauceli, Amy B. Emerman, Kruti M. Patel
Publikováno v:
Cancer Research. 78:1422-1422
Comprehensive genetic evaluation of patients with blood cancer can be imperative for identifying and classifying myeloid malignancies in a patient. Since liquid tumors comprise of highly variable percentages of normal cells or multiple tumor clones,
Autor:
Scott M. Adams, Theodore B. Davis, Charles Elfe, Amy B. Emerman, Andrew Barry, Sarah K. Bowman, Noa Henig, Kruti M. Patel, Cynthia L. Hendrickson, Salvatore Russello
Publikováno v:
Cancer Research. 77:5362-5362
The screening and detection of germline BRCA1 and BRCA2 mutations are critical for the effective management of patients with breast or ovarian cancer and for the identification of individuals with a high risk of developing these cancers. In addition,
Autor:
Charles Elfe, Cynthia L. Hendrickson, Scott V. Adams, Kruti M. Patel, Sarah K. Bowman, Salvatore Russello, Noa Henig, Ted B. Davis, Andrew Barry, Amy B. Emerman
Publikováno v:
Cancer Research. 77:495-495
Variations in copy number are the most common type of DNA structural variations. Many of these alterations are associated with disease or indicate disease susceptibility. Detection of copy number variants (CNVs) for clinical applications requires eff
Autor:
Scott V. Adams, Cynthia L. Hendrickson, Theodore B. Davis, Noa Henig, Fiona A. Stewart, Kruti M. Patel, Sarah K. Bowman, Andrew Barry, Amy B. Emerman, Eileen T. Dimalanta, Charles Elfe
Publikováno v:
Cancer Research. 77:5361-5361
Efficient utilization of targeted gene panels for oncology research is challenged by the wide variation in gene constituents specific to a given study. While focused gene panels efficiently provide the necessary depth of coverage for low frequency va