(Q38407293)

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A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinoma

scientific article published on 25 October 2011

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scholarly article

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Europe PubMed Central

2 September 2017

A computational index derived from whole-genome copy number analysis is a novel tool for prognosis in early stage lung squamous cell carcinoma (English)

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Europe PubMed Central

2 September 2017

whole genome sequencing

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based on heuristic

inferred from title

5

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Rebecca Chalkley

object named as

Rebecca Chalkley

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Stefano Berri

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Jessica Menis

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object named as

Henry M Wood

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Federica Pisa

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author name string

Ornella Belvedere

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Caroline Conway

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Kenneth MacLennan

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Europe PubMed Central

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Catherine Daly

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Europe PubMed Central

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Melissa Alsop

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Europe PubMed Central

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Joanne Morgan

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Europe PubMed Central

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Peter Tcherveniakov

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Europe PubMed Central

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Kostas Papagiannopoulos

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Pamela Rabbitts

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publication date

25 October 2011

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99

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18-24

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1

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Lung cancer cell lines as tools for biomedical discovery and research

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7 January 2021

Catalogue of chromosome aberrations in cancer

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Should we continue to use the term non-small-cell lung cancer?

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Integrative genomic analyses identify BRF2 as a novel lineage-specific oncogene in lung squamous cell carcinoma

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Frequent and focal FGFR1 amplification associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer.

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7 January 2021

Molecular predictive and prognostic markers in non-small-cell lung cancer.

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7 January 2021

A gene expression signature predicts survival of patients with stage I non-small cell lung cancer

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7 January 2021

A five-gene signature and clinical outcome in non-small-cell lung cancer

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Non-overlapping and non-cell-type-specific gene expression signatures predict lung cancer survival

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Genome-wide screening of genomic alterations and their clinicopathologic implications in non-small cell lung cancers

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Genome-wide analysis of survival in early-stage non-small-cell lung cancer

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Novel patterns of genome rearrangement and their association with survival in breast cancer

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Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens

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7 January 2021

TNM Classification of Malignant Tumors, fifth edition (1997). Union Internationale Contre le Cancer and the American Joint Committee on Cancer

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Fast and accurate short read alignment with Burrows-Wheeler transform

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A map of human genome variation from population-scale sequencing

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A faster circular binary segmentation algorithm for the analysis of array CGH data

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KC-SMARTR: An R package for detection of statistically significant aberrations in multi-experiment aCGH data.

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

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7 January 2021

A probe-density-based analysis method for array CGH data: simulation, normalization and centralization.

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Nonparametric Estimation from Incomplete Observations

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7 January 2021

Mutations in the DDR2 kinase gene identify a novel therapeutic target in squamous cell lung cancer

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7 January 2021

CGHcall: calling aberrations for array CGH tumor profiles.

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7 January 2021

CGHnormaliter: an iterative strategy to enhance normalization of array CGH data with imbalanced aberrations

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7 January 2021

Preprocessing and downstream analysis of microarray DNA copy number profiles

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7 January 2021

Haplo-insufficiency: a driving force in cancer

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7 January 2021

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10.1016/J.YGENO.2011.10.006

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Europe PubMed Central

2 September 2017

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Europe PubMed Central

2 September 2017

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