Cancer genomics: one cell at a time

Por Navin, Nicholas E
Publicado no Genome Biol (2014)

The first five years of single-cell cancer genomics and beyond

Por Navin, Nicholas E.
Publicado no Genome Res (2015)

Delineating cancer evolution with single cell sequencing

Por Navin, Nicholas E.
Publicado no Sci Transl Med (2015)

Tumor Evolution in Response to Chemotherapy: Phenotype versus Genotype

Por Navin, Nicholas E.
Publicado no Cell Rep (2014)

Future medical applications of single-cell sequencing in cancer

Por Navin, Nicholas, Hicks, James
Publicado em 2011

Tracing the tumor lineage

Por Navin, Nicholas E., Hicks, James
Publicado em 2010

Advances and Applications of Single Cell Sequencing Technologies

Por Wang, Yong, Navin, Nicholas E.
Publicado no Mol Cell (2015)

Computing tumor trees from single cells

Por Davis, Alexander, Navin, Nicholas E.
Publicado no Genome Biol (2016)

Corrigendum to “Tracing the tumor lineage” [Mol. Oncol. 4 (2010) 267–283]

Por Navin, Nicholas E., Hicks, James
Publicado no Mol Oncol (2011)

Tumor evolution: Linear, branching, neutral or punctuated?()

Por Davis, Alexander, Gao, Ruli, Navin, Nicholas
Publicado no Biochim Biophys Acta (2017)

Genome evolution in ductal carcinoma in situ: invasion of the clones

Por Casasent, Anna, Edgerton, Mary, Navin, Nicholas E.
Publicado no J Pathol (2016)

SNES: single nucleus exome sequencing

Por Leung, Marco L, Wang, Yong, Waters, Jill, Navin, Nicholas E
Publicado no Genome Biol (2015)

Monovar: single nucleotide variant detection in single cells

Por Zafar, Hamim, Wang, Yong, Nakhleh, Luay, Navin, Nicholas, Chen, Ken
Publicado no Nat Methods (2016)

SiFit: inferring tumor trees from single-cell sequencing data under finite-sites models

Por Zafar, Hamim, Tzen, Anthony, Navin, Nicholas, Chen, Ken, Nakhleh, Luay
Publicado no Genome Biol (2017)

Insight into the heterogeneity of breast cancer through next-generation sequencing

Por Russnes, Hege G., Navin, Nicholas, Hicks, James, Borresen-Dale, Anne-Lise
Publicado em 2011

Distribution of short paired duplications in mammalian genomes

Por Thomas, Elizabeth E., Srebro, Nathan, Sebat, Jonathan, Navin, Nicholas, Healy, John, Mishra, Bud, Wigler, Michael
Publicado em 2004

Highly multiplexed targeted DNA sequencing from single nuclei

Por Leung, Marco L, Wang, Yong, Kim, Charissa, Gao, Ruli, Jiang, Jerry, Sei, Emi, Navin, Nicholas E
Publicado no Nat Protoc (2016)

Ploidy-Seq: inferring mutational chronology by sequencing polyploid tumor subpopulations

Por Malhotra, Ankit, Wang, Yong, Waters, Jill, Chen, Ken, Meric-Bernstam, Funda, Hall, Ira M, Navin, Nicholas E
Publicado no Genome Med (2015)

Nanogrid single-nucleus RNA sequencing reveals phenotypic diversity in breast cancer

Por Gao, Ruli, Kim, Charissa, Sei, Emi, Foukakis, Theodoros, Crosetto, Nicola, Chan, Leong-Keat, Srinivasan, Maithreyan, Zhang, Hong, Meric-Bernstam, Funda, Navin, Nicholas
Publicado no Nat Commun (2017)

Single-cell DNA sequencing reveals a late-dissemination model in metastatic colorectal cancer

Por Leung, Marco L., Davis, Alexander, Gao, Ruli, Casasent, Anna, Wang, Yong, Sei, Emi, Vilar, Eduardo, Maru, Dipen, Kopetz, Scott, Navin, Nicholas E.
Publicado no Genome Res (2017)