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Jacob Durtschi

Showing results (1-10 of 13) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 17, 2019
Genome-Wide Copy Number Variation Detection Using NGS: Data Analysis and InterpretationWei Shen, Philippe Szankasi, Jacob Durtschi, et al.
Journal of Biomolecular Techniques : JBT|July 2, 2010
Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genesShale Dames, Jacob Durtschi, Katherine Geiersbach, et al.
Bioinformatics (Oxford, England)|September 19, 2024
Generative haplotype prediction outperforms statistical methods for small variant detection in next-generation sequencing dataBrendan O'Fallon, Ashini Bolia, Jacob Durtschi, et al.
BMC Bioinformatics|July 19, 2022
Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing dataBrendan O'Fallon, Jacob Durtschi, Ana Kellogg, et al.
BMC Bioinformatics|November 26, 2013
VarBin, a novel method for classifying true and false positive variants in NGS dataJacob Durtschi, Rebecca L Margraf, Emily M Coonrod, et al.
American Journal of Clinical Pathology|February 6, 2007
Closed-tube SNP genotyping without labeled probes/a comparison between unlabeled probe and amplicon meltingMichael Liew, Michael Seipp, Jacob Durtschi, et al.
American Journal of Clinical Pathology|December 10, 2022
Morphologic Characteristics and Mutational Analysis of Fumarate Hydratase Deficient Kidney and Smooth Muscle TumorsValarie McMurtry, Jonathan Mahlow, Joshua F Coleman, et al.
The Journal of Allergy and Clinical Immunology|October 19, 2020
CXXC5 variant in an immunodeficient patient with a progressive loss of hematopoietic cellsHemant R Joshi, Harry R Hill, Julie Asch, et al.
Cytometry. Part B, Clinical Cytometry|February 27, 2025
Clinical validation of a real-time machine learning-based system for the detection of acute myeloid leukemia by flow cytometryLauren M Zuromski, Jacob Durtschi, Aimal Aziz, et al.
Child Neurology Open|July 27, 2018
Novel <i>PLP1</i> Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical PhenotypesRebecca L Margraf, Jacob Durtschi, Bryan Krock, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Methods in Molecular Biology (Clifton, N.J.)|January 17, 2019
Genome-Wide Copy Number Variation Detection Using NGS: Data Analysis and InterpretationWei Shen, Philippe Szankasi, Jacob Durtschi, et al.
Journal of Biomolecular Techniques : JBT|July 2, 2010
Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genesShale Dames, Jacob Durtschi, Katherine Geiersbach, et al.
Bioinformatics (Oxford, England)|September 19, 2024
Generative haplotype prediction outperforms statistical methods for small variant detection in next-generation sequencing dataBrendan O'Fallon, Ashini Bolia, Jacob Durtschi, et al.
BMC Bioinformatics|July 19, 2022
Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing dataBrendan O'Fallon, Jacob Durtschi, Ana Kellogg, et al.
BMC Bioinformatics|November 26, 2013
VarBin, a novel method for classifying true and false positive variants in NGS dataJacob Durtschi, Rebecca L Margraf, Emily M Coonrod, et al.
American Journal of Clinical Pathology|February 6, 2007
Closed-tube SNP genotyping without labeled probes/a comparison between unlabeled probe and amplicon meltingMichael Liew, Michael Seipp, Jacob Durtschi, et al.
American Journal of Clinical Pathology|December 10, 2022
Morphologic Characteristics and Mutational Analysis of Fumarate Hydratase Deficient Kidney and Smooth Muscle TumorsValarie McMurtry, Jonathan Mahlow, Joshua F Coleman, et al.
The Journal of Allergy and Clinical Immunology|October 19, 2020
CXXC5 variant in an immunodeficient patient with a progressive loss of hematopoietic cellsHemant R Joshi, Harry R Hill, Julie Asch, et al.
Cytometry. Part B, Clinical Cytometry|February 27, 2025
Clinical validation of a real-time machine learning-based system for the detection of acute myeloid leukemia by flow cytometryLauren M Zuromski, Jacob Durtschi, Aimal Aziz, et al.
Child Neurology Open|July 27, 2018
Novel <i>PLP1</i> Mutations Identified With Next-Generation Sequencing Expand the Spectrum of PLP1-Associated Leukodystrophy Clinical PhenotypesRebecca L Margraf, Jacob Durtschi, Bryan Krock, et al.
Pageof 2