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Mark R Theilmann

Showing results (1-10 of 6) with videos related to

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Clinical Chemistry|August 20, 2016
Group Testing Approach for Trinucleotide Repeat Expansion Disorder ScreeningKristjan Eerik Kaseniit, Mark R Theilmann, Alexander Robertson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 15, 2020
High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screeningNoah C Welker, Albert K Lee, Rachel A S Kjolby, et al.
BMC Medical Genetics|October 1, 2018
Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogeneGenevieve M Gould, Peter V Grauman, Mark R Theilmann, et al.
Peerj|March 1, 2017
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessmentValentina S Vysotskaia, Gregory J Hogan, Genevieve M Gould, et al.
Clinical Chemistry|May 16, 2018
Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant IdentificationGregory J Hogan, Valentina S Vysotskaia, Kyle A Beauchamp, et al.
Journal of Biological Engineering|June 22, 2012
A BioBrick compatible strategy for genetic modification of plantsPatrick M Boyle, Devin R Burrill, Mara C Inniss, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Clinical Chemistry|August 20, 2016
Group Testing Approach for Trinucleotide Repeat Expansion Disorder ScreeningKristjan Eerik Kaseniit, Mark R Theilmann, Alexander Robertson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 15, 2020
High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screeningNoah C Welker, Albert K Lee, Rachel A S Kjolby, et al.
BMC Medical Genetics|October 1, 2018
Detecting clinically actionable variants in the 3' exons of PMS2 via a reflex workflow based on equivalent hybrid capture of the gene and its pseudogeneGenevieve M Gould, Peter V Grauman, Mark R Theilmann, et al.
Peerj|March 1, 2017
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessmentValentina S Vysotskaia, Gregory J Hogan, Genevieve M Gould, et al.
Clinical Chemistry|May 16, 2018
Validation of an Expanded Carrier Screen that Optimizes Sensitivity via Full-Exon Sequencing and Panel-wide Copy Number Variant IdentificationGregory J Hogan, Valentina S Vysotskaia, Kyle A Beauchamp, et al.
Journal of Biological Engineering|June 22, 2012
A BioBrick compatible strategy for genetic modification of plantsPatrick M Boyle, Devin R Burrill, Mara C Inniss, et al.
Pageof 1