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Whole-genome sequencing of nine esophageal adenocarcinoma cell lines

Contino, G; Eldridge, MD; Secrier, M; Bower, L; Fels Elliott, R; Weaver, J; Lynch, AG; ... Fitzgerald, RC; + view all (2016) Whole-genome sequencing of nine esophageal adenocarcinoma cell lines. F1000Research , 5 , Article 1336. 10.12688/f1000research.7033.1. Green open access

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Abstract

Esophageal adenocarcinoma (EAC) is highly mutated and molecularly heterogeneous. The number of cell lines available for study is limited and their genome has been only partially characterized. The availability of an accurate annotation of their mutational landscape is crucial for accurate experimental design and correct interpretation of genotype-phenotype findings. We performed high coverage, paired end whole genome sequencing on eight EAC cell lines-ESO26, ESO51, FLO-1, JH-EsoAd1, OACM5.1 C, OACP4 C, OE33, SK-GT-4-all verified against original patient material, and one esophageal high grade dysplasia cell line, CP-D. We have made available the aligned sequence data and report single nucleotide variants (SNVs), small insertions and deletions (indels), and copy number alterations, identified by comparison with the human reference genome and known single nucleotide polymorphisms (SNPs). We compare these putative mutations to mutations found in primary tissue EAC samples, to inform the use of these cell lines as a model of EAC.

Type: Article
Title: Whole-genome sequencing of nine esophageal adenocarcinoma cell lines
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.12688/f1000research.7033.1
Publisher version: http://doi.org/10.12688/f1000research.7033.1
Language: English
Additional information: © 2016 Contino G et al. This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: Esophageal adenocarcinoma, cancer genome, cell line, copy number alteration, high-grade dysplasia, single nucleotide variant, whole genome sequencing
UCL classification: UCL
UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences > Genetics, Evolution and Environment
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10037720
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