Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Karyn Meltz Steinberg

Showing results (1-10 of 22) with videos related to

Pageof 3
Sort By:
Proceedings. Biological Sciences|May 31, 2007
Grazing protozoa and the evolution of the Escherichia coli O157:H7 Shiga toxin-encoding prophageKaryn Meltz Steinberg, Bruce R Levin
Analytical Chemistry|March 6, 2008
Applying rapid genome sequencing technologies to characterize pathogen genomesKaryn Meltz Steinberg, David T Okou, Michael E Zwick
Scientific Reports|March 17, 2015
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALSKaryn Meltz Steinberg, Bing Yu, Daniel C Koboldt, et al.
Cell|October 1, 2013
The next-generation sequencing revolution and its impact on genomicsDaniel C Koboldt, Karyn Meltz Steinberg, David E Larson, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 12, 2015
Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosisKaryn Meltz Steinberg, Thomas J Nicholas, Daniel C Koboldt, et al.
Molecular Autism|October 2, 2012
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderKaryn Meltz Steinberg, Dhanya Ramachandran, Viren C Patel, et al.
Nature Methods|October 16, 2007
Microarray-based genomic selection for high-throughput resequencingDavid T Okou, Karyn Meltz Steinberg, Christina Middle, et al.
Blood Advances|November 9, 2018
A novel <i>FAS</i> mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman diseaseTurner S Baker, Kristyne J Gambino, Lawrence Schriefer, et al.
BMC Bioinformatics|September 22, 2010
SeqAnt: a web service to rapidly identify and annotate DNA sequence variationsAmol Carl Shetty, Prashanth Athri, Kajari Mondal, et al.
Genes and Immunity|October 24, 2014
Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversityCorey T Watson, Karyn Meltz Steinberg, Tina A Graves, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Proceedings. Biological Sciences|May 31, 2007
Grazing protozoa and the evolution of the Escherichia coli O157:H7 Shiga toxin-encoding prophageKaryn Meltz Steinberg, Bruce R Levin
Analytical Chemistry|March 6, 2008
Applying rapid genome sequencing technologies to characterize pathogen genomesKaryn Meltz Steinberg, David T Okou, Michael E Zwick
Scientific Reports|March 17, 2015
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALSKaryn Meltz Steinberg, Bing Yu, Daniel C Koboldt, et al.
Cell|October 1, 2013
The next-generation sequencing revolution and its impact on genomicsDaniel C Koboldt, Karyn Meltz Steinberg, David E Larson, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 12, 2015
Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosisKaryn Meltz Steinberg, Thomas J Nicholas, Daniel C Koboldt, et al.
Molecular Autism|October 2, 2012
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderKaryn Meltz Steinberg, Dhanya Ramachandran, Viren C Patel, et al.
Nature Methods|October 16, 2007
Microarray-based genomic selection for high-throughput resequencingDavid T Okou, Karyn Meltz Steinberg, Christina Middle, et al.
Blood Advances|November 9, 2018
A novel <i>FAS</i> mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman diseaseTurner S Baker, Kristyne J Gambino, Lawrence Schriefer, et al.
BMC Bioinformatics|September 22, 2010
SeqAnt: a web service to rapidly identify and annotate DNA sequence variationsAmol Carl Shetty, Prashanth Athri, Kajari Mondal, et al.
Genes and Immunity|October 24, 2014
Sequencing of the human IG light chain loci from a hydatidiform mole BAC library reveals locus-specific signatures of genetic diversityCorey T Watson, Karyn Meltz Steinberg, Tina A Graves, et al.
Pageof 3