Sensitivity to sequencing depth in single-cell cancer genomics-Reference-Cited by-同舟云学术

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Sensitivity to sequencing depth in single-cell cancer genomics

Published:2018-04-16 Issue:1 Volume:10 Page:
ISSN:1756-994X
Container-title:Genome Medicine
language:en
Short-container-title:Genome Med

Author:

Alves João M.,Posada David

Funder

Consellería de Cultura, Educación e Ordenación Universitaria, Xunta de Galicia

European Research Council

Secretaría de Estado de Investigación, Desarrollo e Innovación

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13073-018-0537-2.pdf

Reference41 articles.

1. Gerlinger M, Swanton C. How Darwinian models inform therapeutic failure initiated by clonal heterogeneity in cancer medicine. Br J Cancer. 2010;103:1139–43.

2. Navin NE. Cancer genomics: one cell at a time. Genome Biol. 2014;15:452.

3. Potter NE, Ermini L, Papaemmanuil E, Cazzaniga G, Vijayaraghavan G, Titley I, et al. Single-cell mutational profiling and clonal phylogeny in cancer. Genome Res. 2013;23:2115–25.

4. Hughes AEO, Magrini V, Demeter R, Miller CA, Fulton R, Fulton LL, et al. Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencing. PLoS Genet. 2014;10:e1004462.

5. Wang Y, Waters J, Leung ML, Unruh A, Roh W, Shi X, et al. Clonal evolution in breast cancer revealed by single nucleus genome sequencing. Nature. 2014;512:155–60.

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3. Single-Cell Sequencing in Cancer Research: Challenges and Opportunities;Handbook of Cancer and Immunology;2023

4. BiTSC 2: Bayesian inference of tumor clonal tree by joint analysis of single-cell SNV and CNA data;Briefings in Bioinformatics;2022-04-02

5. Sensitivity to copy number variation analysis in single cell genomics;Gene;2022-01

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