Eric J Duncavage

Summary

Publications

  1. pmc Hybrid capture and next-generation sequencing identify viral integration sites from formalin-fixed, paraffin-embedded tissue
    Eric J Duncavage
    Department of Pathology, University of Utah, 500 Chipeta Way, Salt Lake, UT 84108, USA
    J Mol Diagn 13:325-33. 2011
  2. doi request reprint SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data
    Haley J Abel
    Department of Internal Medicine, Division of Genetic Epidemiology, Department of Pathology, University of Utah, Salt Lake City, UT, USA
    Bioinformatics 26:2684-8. 2010
  3. doi request reprint Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimens
    David H Spencer
    Department of Pathology, Washington University School of Medicine, St Louis, Missouri, USA
    J Mol Diagn 15:623-33. 2013
  4. doi request reprint Merkel cell polyomavirus (MCPyV) in chronic lymphocytic leukemia/small lymphocytic lymphoma
    Carolin J Teman
    Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA
    Leuk Res 35:689-92. 2011
  5. doi request reprint MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors
    Katherine E Schwetye
    Department of Pathology, Washington University School of Medicine, St Louis, MO 63110, USA
    Hum Pathol 45:65-70. 2014

Collaborators

  • John D Pfeifer
  • Haley J Abel
  • Katherine E Schwetye
  • David H Spencer
  • Carolin J Teman
  • Jennifer K Sehn
  • Mark A Watson
  • Sheryl R Tripp
  • Sherrie L Perkins
  • Vincent J Magrini
  • Nils Becker
  • Jon R Armstrong

Detail Information

Publications5

  1. pmc Hybrid capture and next-generation sequencing identify viral integration sites from formalin-fixed, paraffin-embedded tissue
    Eric J Duncavage
    Department of Pathology, University of Utah, 500 Chipeta Way, Salt Lake, UT 84108, USA
    J Mol Diagn 13:325-33. 2011
    ....
  2. doi request reprint SLOPE: a quick and accurate method for locating non-SNP structural variation from targeted next-generation sequence data
    Haley J Abel
    Department of Internal Medicine, Division of Genetic Epidemiology, Department of Pathology, University of Utah, Salt Lake City, UT, USA
    Bioinformatics 26:2684-8. 2010
    ..Existing 'next-gen' sequencing analysis packages are optimized for efficiency in whole-genome studies and are unable to benefit from the particular structure of targeted sequence data...
  3. doi request reprint Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimens
    David H Spencer
    Department of Pathology, Washington University School of Medicine, St Louis, Missouri, USA
    J Mol Diagn 15:623-33. 2013
    ..This study demonstrates that routine processing of FFPE samples has a detectable but negligible effect on NGS data and that these samples can be a reliable substrate for clinical NGS testing. ..
  4. doi request reprint Merkel cell polyomavirus (MCPyV) in chronic lymphocytic leukemia/small lymphocytic lymphoma
    Carolin J Teman
    Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA
    Leuk Res 35:689-92. 2011
    ..MCPyV was not identified in 17 cases of follicular lymphoma, suggesting either that MCPyV is involved in CLL/SLL pathogenesis or that the immunodeficiency state of CLL/SLL induces low-level MCPyV reactivation...
  5. doi request reprint MED12 exon 2 mutations in uterine and extrauterine smooth muscle tumors
    Katherine E Schwetye
    Department of Pathology, Washington University School of Medicine, St Louis, MO 63110, USA
    Hum Pathol 45:65-70. 2014
    ....