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Nicholas Navin

Showing results (11-20 of 51) with videos related to

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Genome Biology|September 21, 2017
SiFit: inferring tumor trees from single-cell sequencing data under finite-sites modelsHamim Zafar, Anthony Tzen, Nicholas Navin, et al.
The Journal of Clinical Investigation|October 4, 2011
Insight into the heterogeneity of breast cancer through next-generation sequencingHege G Russnes, Nicholas Navin, James Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 9, 2004
Distribution of short paired duplications in mammalian genomesElizabeth E Thomas, Nathan Srebro, Jonathan Sebat, et al.
Cancer Journal (Sudbury, Mass.)|July 30, 2011
Toward an integrated knowledge environment to support modern oncologyPatrick M Blake, David A Decker, Timothy M Glennon, et al.
Nature Communications|August 11, 2017
Nanogrid single-nucleus RNA sequencing reveals phenotypic diversity in breast cancerRuli Gao, Charissa Kim, Emi Sei, et al.
Genome Biology|February 24, 2021
MEDALT: single-cell copy number lineage tracing enabling gene discoveryFang Wang, Qihan Wang, Vakul Mohanty, et al.
Bioinformatics (Oxford, England)|June 3, 2006
PROBER: oligonucleotide FISH probe design softwareNicholas Navin, Vladimir Grubor, Jim Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 2006
Identification of alterations in DNA copy number in host stromal cells during tumor progressionRobert J Pelham, Linda Rodgers, Ira Hall, et al.
Nature Protocols|February 26, 2016
Corrigendum: Genome-wide copy number analysis of single cellsTimour Baslan, Jude Kendall, Linda Rodgers, et al.
Nature Protocols|May 5, 2012
Genome-wide copy number analysis of single cellsTimour Baslan, Jude Kendall, Linda Rodgers, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Genome Biology|September 21, 2017
SiFit: inferring tumor trees from single-cell sequencing data under finite-sites modelsHamim Zafar, Anthony Tzen, Nicholas Navin, et al.
The Journal of Clinical Investigation|October 4, 2011
Insight into the heterogeneity of breast cancer through next-generation sequencingHege G Russnes, Nicholas Navin, James Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 9, 2004
Distribution of short paired duplications in mammalian genomesElizabeth E Thomas, Nathan Srebro, Jonathan Sebat, et al.
Cancer Journal (Sudbury, Mass.)|July 30, 2011
Toward an integrated knowledge environment to support modern oncologyPatrick M Blake, David A Decker, Timothy M Glennon, et al.
Nature Communications|August 11, 2017
Nanogrid single-nucleus RNA sequencing reveals phenotypic diversity in breast cancerRuli Gao, Charissa Kim, Emi Sei, et al.
Genome Biology|February 24, 2021
MEDALT: single-cell copy number lineage tracing enabling gene discoveryFang Wang, Qihan Wang, Vakul Mohanty, et al.
Bioinformatics (Oxford, England)|June 3, 2006
PROBER: oligonucleotide FISH probe design softwareNicholas Navin, Vladimir Grubor, Jim Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 15, 2006
Identification of alterations in DNA copy number in host stromal cells during tumor progressionRobert J Pelham, Linda Rodgers, Ira Hall, et al.
Nature Protocols|February 26, 2016
Corrigendum: Genome-wide copy number analysis of single cellsTimour Baslan, Jude Kendall, Linda Rodgers, et al.
Nature Protocols|May 5, 2012
Genome-wide copy number analysis of single cellsTimour Baslan, Jude Kendall, Linda Rodgers, et al.
Pageof 6