Single-cell sequencing of genomic DNA resolves sub-clonal heterogeneity in a melanoma cell line

Whole-genome landscape of mucosal melanoma reveals diverse drivers and therapeutic targets

(2019) Felicity Newell et al.   Nature Communications

Detection of Copy Number Alterations Using Single Cell Sequencing

(2017) Kristin A. Knouse et al.   Jove-Journal of Visualized Experiments

Assessment of megabase-scale somatic copy number variation using single-cell sequencing

(2016) Kristin A. Knouse et al.   GENOME RESEARCH

Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance

(2016) Maria Secrier et al.   NATURE GENETICS

A somatic reference standard for cancer genome sequencing

(2016) David W. Craig et al.   Scientific Reports

Clonal evolution in breast cancer revealed by single nucleus genome sequencing

(2014) Yong Wang et al.   NATURE

Long insert whole genome sequencing for copy number variant and translocation detection

(2013) Winnie S. Liang et al.   NUCLEIC ACIDS RESEARCH

Correcting for cancer genome size and tumour cell content enables better estimation of copy number alterations from next-generation sequence data

(2011) Arief Gusnanto et al.   BIOINFORMATICS

CREST maps somatic structural variation in cancer genomes with base-pair resolution

(2011) Jianmin Wang et al.   NATURE METHODS

Single-cell copy number variation detection

(2011) Jiqiu Cheng et al.   GENOME BIOLOGY

A comprehensive catalogue of somatic mutations from a human cancer genome

(2009) Erin D. Pleasance et al.   NATURE