Tumour evolution inferred by single-cell sequencing
By N. Navin, J. Kendall, J. Troge, Peter A. Andrews, L. Rodgers, J. McIndoo, K. Cook, A. Stepansky, D. Levy, D. Esposito and 5 more. Nature, 2011
2,594 citations recorded by the source corpus.
Subfields: Cancer Research, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/807307141ba49471fbce69662a1ad601a3ab7fbb
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Cancer Research
- Charles Swanton
- Nicholas McGranahan
- Gad Getz
- Peter J. Campbell
- Dominic Grün
- Alexander van Oudenaarden
- Daniel C. Koboldt
- S. Nik-Zainal
In Genetics
- Pavel A. Pevzner
- Alexander van Oudenaarden
- Dmitry Antipov
- Dominic Grün
- Charles Swanton
- Nicholas McGranahan
- Peter W. Laird
- R. Weinberg
In Molecular Biology
- Pavel A. Pevzner
- Nicholas McGranahan
- Charles Swanton
- Alexander van Oudenaarden
- Eric S. Lander
- Dominic Grün
- Peter W. Laird
- R. Weinberg
Citations in the corpus
- Evolution and impact of subclonal mutations in chronic lymphocytic leukemia (2013, positive): “Recent genomic studies have revealed that individual cancer samples are genetically heterogeneous and contain subclonal populations (Carter et al., 2012; Ding et al., 2012; Gerlinger et al., 2012; Mullighan et al., 2008; Navin et al., 2011; Nik-Zainal et al., 2012; Shah et al., 2012).”
- Clonal Evolution in Breast Cancer Revealed by Single Nucleus Genome Sequencing (2014, methodology): “We flow-sorted 50 single nuclei from the H, D and A ploidy distributions for copy number profiling using SNS (Fig.”
- Mapping the Mouse Cell Atlas by Microwell-Seq. (2018, positive): “Other methodologies, such as single-cell genome analysis (Hou et al., 2012; Navin et al., 2011; Wang et al., 2012; Xu et al., 2012), epigenome analysis (Buenrostro et al.”
- Clonal evolution in relapsed acute myeloid leukemia revealed by whole genome sequencing (2012, positive): “…who recently described patterns of clonal evolution in ALL patients using FISH and/or copy number alterations detected by SNP arrays, and it enhances the understanding of genetic changes acquired during disease progression, as previously described for breast and pancreatic cancer metastases 22–25 .”
- Signal transduction in cancer. (2015, neutral): “…from sequencing of single cells and multiple regions of tumors from individual patients has revealed this is far greater than previously imagined (Navin et al. 2011; Ruiz et al. 2011; Ding et al. 2012; Gerlinger et al. 2012; Xu et al. 2012b; Bashashati et al. 2013) In one study of kidney tumors,…”
- A deep generative model for gene expression profiles from single-cell RNA sequencing (2017, background): “Therefore, single-cell experiments took gene expression understanding to the next level with applications in immunology [4], oncology [5] and other subfields of biology [6].”
- SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing (2012, background): “…in 2011 have opened the possibilities of performing genome-wide haplotyping (Fan et al., 2011), studying heterogeneity within stem cell and tumor populations (Dalerba et al., 2011), tracing tumor evolution (Navin et al., 2011), and characterizing a single-cell transcriptome (Islam et al., 2011).”