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Travis M Drucker

Showing results (1-10 of 9) with videos related to

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Bioinformatics (Oxford, England)|February 15, 2014
BIMA V3: an aligner customized for mate pair library sequencingTravis M Drucker, Sarah H Johnson, Stephen J Murphy, et al.
BMC Medical Genetics|February 8, 2014
A simple method for gene phasing using mate pair sequencingKendall W Cradic, Stephen J Murphy, Travis M Drucker, et al.
Journal of Clinical Microbiology|April 14, 2017
Comparison of Whole-Genome Sequencing Methods for Analysis of Three Methicillin-Resistant Staphylococcus aureus OutbreaksScott A Cunningham, Nicholas Chia, Patricio R Jeraldo, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 12, 2014
Identification of independent primary tumors and intrapulmonary metastases using DNA rearrangements in non-small-cell lung cancerStephen J Murphy, Marie-Christine Aubry, Faye R Harris, et al.
Genes, Chromosomes & Cancer|May 5, 2018
Copy number variant analysis using genome-wide mate-pair sequencingJames B Smadbeck, Sarah H Johnson, Stephanie A Smoley, et al.
BMC Bioinformatics|November 10, 2019
Recommendations for performance optimizations when using GATK3.8 and GATK4Jacob R Heldenbrand, Saurabh Baheti, Matthew A Bockol, et al.
BMC Bioinformatics|December 19, 2019
Correction to: Recommendations for performance optimizations when using GATK3.8 and GATK4Jacob R Heldenbrand, Saurabh Baheti, Matthew A Bockol, et al.
Frontiers in Genetics|September 5, 2019
Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and AccuracyKatherine I Kendig, Saurabh Baheti, Matthew A Bockol, et al.
Cancer Genetics|February 7, 2018
SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq)Sarah H Johnson, James B Smadbeck, Stephanie A Smoley, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Bioinformatics (Oxford, England)|February 15, 2014
BIMA V3: an aligner customized for mate pair library sequencingTravis M Drucker, Sarah H Johnson, Stephen J Murphy, et al.
BMC Medical Genetics|February 8, 2014
A simple method for gene phasing using mate pair sequencingKendall W Cradic, Stephen J Murphy, Travis M Drucker, et al.
Journal of Clinical Microbiology|April 14, 2017
Comparison of Whole-Genome Sequencing Methods for Analysis of Three Methicillin-Resistant Staphylococcus aureus OutbreaksScott A Cunningham, Nicholas Chia, Patricio R Jeraldo, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 12, 2014
Identification of independent primary tumors and intrapulmonary metastases using DNA rearrangements in non-small-cell lung cancerStephen J Murphy, Marie-Christine Aubry, Faye R Harris, et al.
Genes, Chromosomes & Cancer|May 5, 2018
Copy number variant analysis using genome-wide mate-pair sequencingJames B Smadbeck, Sarah H Johnson, Stephanie A Smoley, et al.
BMC Bioinformatics|November 10, 2019
Recommendations for performance optimizations when using GATK3.8 and GATK4Jacob R Heldenbrand, Saurabh Baheti, Matthew A Bockol, et al.
BMC Bioinformatics|December 19, 2019
Correction to: Recommendations for performance optimizations when using GATK3.8 and GATK4Jacob R Heldenbrand, Saurabh Baheti, Matthew A Bockol, et al.
Frontiers in Genetics|September 5, 2019
Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and AccuracyKatherine I Kendig, Saurabh Baheti, Matthew A Bockol, et al.
Cancer Genetics|February 7, 2018
SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq)Sarah H Johnson, James B Smadbeck, Stephanie A Smoley, et al.
Pageof 1