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Michael E Zwick

Showing results (21-30 of 75) with videos related to

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Human Molecular Genetics|July 10, 2012
Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorderKajari Mondal, Dhanya Ramachandran, Viren C Patel, et al.
Scientific Reports|February 23, 2012
Genetic variation and linkage disequilibrium in Bacillus anthracisMichael E Zwick, Maureen Kiley Thomason, Peter E Chen, et al.
Nucleic Acids Research|April 13, 2017
Omicseq: a web-based search engine for exploring omics datasetsXiaobo Sun, William S Pittard, Tianlei Xu, et al.
Human Mutation|July 30, 2008
Microarray-based mutation detection in the dystrophin geneMadhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, et al.
Scientific Reports|June 26, 2019
Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variantsSuresh Venkateswaran, Lee A Denson, Ingrid Jurickova, et al.
Molecular Autism|July 27, 2019
Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registryRebecca M Pollak, Melissa M Murphy, Michael P Epstein, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed malesStephen C Collins, Steven M Bray, Joshua A Suhl, et al.
G3 (Bethesda, Md.)|March 3, 2012
Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the MouseMiao Sun, Kajari Mondal, Viren Patel, et al.
Genome Biology|January 12, 2005
Microarray-based resequencing of multiple Bacillus anthracis isolatesMichael E Zwick, Farrell Mcafee, David J Cutler, et al.
Annals of Human Genetics|July 4, 2009
Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regionsDavid T Okou, Adam E Locke, Karyn M Steinberg, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|July 10, 2012
Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorderKajari Mondal, Dhanya Ramachandran, Viren C Patel, et al.
Scientific Reports|February 23, 2012
Genetic variation and linkage disequilibrium in Bacillus anthracisMichael E Zwick, Maureen Kiley Thomason, Peter E Chen, et al.
Nucleic Acids Research|April 13, 2017
Omicseq: a web-based search engine for exploring omics datasetsXiaobo Sun, William S Pittard, Tianlei Xu, et al.
Human Mutation|July 30, 2008
Microarray-based mutation detection in the dystrophin geneMadhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, et al.
Scientific Reports|June 26, 2019
Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variantsSuresh Venkateswaran, Lee A Denson, Ingrid Jurickova, et al.
Molecular Autism|July 27, 2019
Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registryRebecca M Pollak, Melissa M Murphy, Michael P Epstein, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed malesStephen C Collins, Steven M Bray, Joshua A Suhl, et al.
G3 (Bethesda, Md.)|March 3, 2012
Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the MouseMiao Sun, Kajari Mondal, Viren Patel, et al.
Genome Biology|January 12, 2005
Microarray-based resequencing of multiple Bacillus anthracis isolatesMichael E Zwick, Farrell Mcafee, David J Cutler, et al.
Annals of Human Genetics|July 4, 2009
Combining microarray-based genomic selection (MGS) with the Illumina Genome Analyzer platform to sequence diploid target regionsDavid T Okou, Adam E Locke, Karyn M Steinberg, et al.
Pageof 8