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Peter N Robinson

Showing results (61-70 of 348) with videos related to

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Bioinformatics (Oxford, England)|February 11, 2010
Microindel detection in short-read sequence dataPeter Krawitz, Christian Rödelsperger, Marten Jäger, et al.
Human Mutation|March 29, 2014
Jannovar: a java library for exome annotationMarten Jäger, Kai Wang, Sebastian Bauer, et al.
Genomics|August 8, 2009
Short ultraconserved promoter regions delineate a class of preferentially expressed alternatively spliced transcriptsChristian Rödelsperger, Sebastian Köhler, Marcel H Schulz, et al.
The International Journal of Biochemistry & Cell Biology|November 13, 2007
A short ultraconserved sequence drives transcription from an alternate FBN1 promoterGao Guo, Sebastian Bauer, Jochen Hecht, et al.
Plos One|September 21, 2017
Biometric and structural ocular manifestations of Marfan syndromePetra Gehle, Barbara Goergen, Daniel Pilger, et al.
The Turkish Journal of Pediatrics|June 28, 2012
Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 geneEsra Kiliç, Yasemin Alanay, Eda Utine, et al.
Genome Research|July 12, 2015
Saturation analysis of ChIP-seq data for reproducible identification of binding peaksPeter Hansen, Jochen Hecht, Daniel M Ibrahim, et al.
Genome Medicine|December 15, 2016
Alternate-locus aware variant calling in whole genome sequencingMarten Jäger, Max Schubach, Tomasz Zemojtel, et al.
Journal of Medical Systems|October 23, 2012
Summarizing phenotype evolution patterns from report casesMaría Taboada, Verónica Alvarez, Diego Martínez, et al.
Database : the Journal of Biological Databases and Curation|October 29, 2015
PhenoMiner: from text to a database of phenotypes associated with OMIM diseasesNigel Collier, Tudor Groza, Damian Smedley, et al.
Pageof 35

Showing results (61-70 of 348) with videos related to

Sort By:
Pageof 35
Bioinformatics (Oxford, England)|February 11, 2010
Microindel detection in short-read sequence dataPeter Krawitz, Christian Rödelsperger, Marten Jäger, et al.
Human Mutation|March 29, 2014
Jannovar: a java library for exome annotationMarten Jäger, Kai Wang, Sebastian Bauer, et al.
Genomics|August 8, 2009
Short ultraconserved promoter regions delineate a class of preferentially expressed alternatively spliced transcriptsChristian Rödelsperger, Sebastian Köhler, Marcel H Schulz, et al.
The International Journal of Biochemistry & Cell Biology|November 13, 2007
A short ultraconserved sequence drives transcription from an alternate FBN1 promoterGao Guo, Sebastian Bauer, Jochen Hecht, et al.
Plos One|September 21, 2017
Biometric and structural ocular manifestations of Marfan syndromePetra Gehle, Barbara Goergen, Daniel Pilger, et al.
The Turkish Journal of Pediatrics|June 28, 2012
Arterial tortuosity and aneurysm in a case of Loeys-Dietz syndrome type IB with a mutation p.R537P in the TGFBR2 geneEsra Kiliç, Yasemin Alanay, Eda Utine, et al.
Genome Research|July 12, 2015
Saturation analysis of ChIP-seq data for reproducible identification of binding peaksPeter Hansen, Jochen Hecht, Daniel M Ibrahim, et al.
Genome Medicine|December 15, 2016
Alternate-locus aware variant calling in whole genome sequencingMarten Jäger, Max Schubach, Tomasz Zemojtel, et al.
Journal of Medical Systems|October 23, 2012
Summarizing phenotype evolution patterns from report casesMaría Taboada, Verónica Alvarez, Diego Martínez, et al.
Database : the Journal of Biological Databases and Curation|October 29, 2015
PhenoMiner: from text to a database of phenotypes associated with OMIM diseasesNigel Collier, Tudor Groza, Damian Smedley, et al.
Pageof 35