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The Journal of Molecular Diagnostics : JMD
|
July 2, 2013
Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimens
David H Spencer, Jennifer K Sehn, Haley J Abel, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
January 11, 2014
Retinoblastoma gene mutations detected by whole exome sequencing of Merkel cell carcinoma
Patrick J Cimino, Diane H Robirds, Sheryl R Tripp, et al.
Genetic Epidemiology
|
December 1, 2011
Effect of linkage disequilibrium on the identification of functional variants
Alun Thomas, Haley J Abel, Yanming Di, et al.
Archives of Pathology & Laboratory Medicine
|
July 9, 2016
A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing
Eric J Duncavage, Haley J Abel, Jason D Merker, et al.
Bioinformatics (Oxford, England)
|
June 21, 2019
svtools: population-scale analysis of structural variation
David E Larson, Haley J Abel, Colby Chiang, et al.
The Journal of Molecular Diagnostics : JMD
|
April 19, 2011
Hybrid capture and next-generation sequencing identify viral integration sites from formalin-fixed, paraffin-embedded tissue
Eric J Duncavage, Vincent Magrini, Nils Becker, et al.
American Journal of Clinical Pathology
|
September 20, 2015
Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing Testing
Jennifer K Sehn, David H Spencer, John D Pfeifer, et al.
Experimental and Molecular Pathology
|
January 18, 2017
Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing
Paul J Lee, Naomi S Yoo, Ian S Hagemann, et al.
Journal of the American Academy of Dermatology
|
June 7, 2015
T-cell clonality assessment by next-generation sequencing improves detection sensitivity in mycosis fungoides
Kari E Sufficool, Christina M Lockwood, Haley J Abel, et al.
Annals of Human Genetics
|
September 20, 2012
Shared genomic segment analysis: the power to find rare disease variants
Stacey Knight, Ryan P Abo, Haley J Abel, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 40) with videos related to
Sort By:
Page
of 4
The Journal of Molecular Diagnostics : JMD
|
July 2, 2013
Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimens
David H Spencer, Jennifer K Sehn, Haley J Abel, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
January 11, 2014
Retinoblastoma gene mutations detected by whole exome sequencing of Merkel cell carcinoma
Patrick J Cimino, Diane H Robirds, Sheryl R Tripp, et al.
Genetic Epidemiology
|
December 1, 2011
Effect of linkage disequilibrium on the identification of functional variants
Alun Thomas, Haley J Abel, Yanming Di, et al.
Archives of Pathology & Laboratory Medicine
|
July 9, 2016
A Model Study of In Silico Proficiency Testing for Clinical Next-Generation Sequencing
Eric J Duncavage, Haley J Abel, Jason D Merker, et al.
Bioinformatics (Oxford, England)
|
June 21, 2019
svtools: population-scale analysis of structural variation
David E Larson, Haley J Abel, Colby Chiang, et al.
The Journal of Molecular Diagnostics : JMD
|
April 19, 2011
Hybrid capture and next-generation sequencing identify viral integration sites from formalin-fixed, paraffin-embedded tissue
Eric J Duncavage, Vincent Magrini, Nils Becker, et al.
American Journal of Clinical Pathology
|
September 20, 2015
Occult Specimen Contamination in Routine Clinical Next-Generation Sequencing Testing
Jennifer K Sehn, David H Spencer, John D Pfeifer, et al.
Experimental and Molecular Pathology
|
January 18, 2017
Spectrum of mutations in leiomyosarcomas identified by clinical targeted next-generation sequencing
Paul J Lee, Naomi S Yoo, Ian S Hagemann, et al.
Journal of the American Academy of Dermatology
|
June 7, 2015
T-cell clonality assessment by next-generation sequencing improves detection sensitivity in mycosis fungoides
Kari E Sufficool, Christina M Lockwood, Haley J Abel, et al.
Annals of Human Genetics
|
September 20, 2012
Shared genomic segment analysis: the power to find rare disease variants
Stacey Knight, Ryan P Abo, Haley J Abel, et al.
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of 4