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Genome Biology
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September 21, 2017
SiFit: inferring tumor trees from single-cell sequencing data under finite-sites models
Hamim 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 sequencing
Hege 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 genomes
Elizabeth E Thomas, Nathan Srebro, Jonathan Sebat, et al.
Cancer Journal (Sudbury, Mass.)
|
July 30, 2011
Toward an integrated knowledge environment to support modern oncology
Patrick 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 cancer
Ruli Gao, Charissa Kim, Emi Sei, et al.
Genome Biology
|
February 24, 2021
MEDALT: single-cell copy number lineage tracing enabling gene discovery
Fang Wang, Qihan Wang, Vakul Mohanty, et al.
Bioinformatics (Oxford, England)
|
June 3, 2006
PROBER: oligonucleotide FISH probe design software
Nicholas 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 progression
Robert J Pelham, Linda Rodgers, Ira Hall, et al.
Nature Protocols
|
February 26, 2016
Corrigendum: Genome-wide copy number analysis of single cells
Timour Baslan, Jude Kendall, Linda Rodgers, et al.
Nature Protocols
|
May 5, 2012
Genome-wide copy number analysis of single cells
Timour Baslan, Jude Kendall, Linda Rodgers, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
Genome Biology
|
September 21, 2017
SiFit: inferring tumor trees from single-cell sequencing data under finite-sites models
Hamim 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 sequencing
Hege 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 genomes
Elizabeth E Thomas, Nathan Srebro, Jonathan Sebat, et al.
Cancer Journal (Sudbury, Mass.)
|
July 30, 2011
Toward an integrated knowledge environment to support modern oncology
Patrick 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 cancer
Ruli Gao, Charissa Kim, Emi Sei, et al.
Genome Biology
|
February 24, 2021
MEDALT: single-cell copy number lineage tracing enabling gene discovery
Fang Wang, Qihan Wang, Vakul Mohanty, et al.
Bioinformatics (Oxford, England)
|
June 3, 2006
PROBER: oligonucleotide FISH probe design software
Nicholas 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 progression
Robert J Pelham, Linda Rodgers, Ira Hall, et al.
Nature Protocols
|
February 26, 2016
Corrigendum: Genome-wide copy number analysis of single cells
Timour Baslan, Jude Kendall, Linda Rodgers, et al.
Nature Protocols
|
May 5, 2012
Genome-wide copy number analysis of single cells
Timour Baslan, Jude Kendall, Linda Rodgers, et al.
Page
of 6