Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data-Reference-Cited by-同舟云学术

Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data

Published:2011-12-06 Issue:3 Volume:28 Page:423-425
ISSN:1460-2059
Container-title:Bioinformatics
language:en
Short-container-title:

Author:

Boeva Valentina,Popova Tatiana,Bleakley Kevin,Chiche Pierre,Cappo Julie,Schleiermacher Gudrun,Janoueix-Lerosey Isabelle,Delattre Olivier,Barillot Emmanuel

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Link

http://academic.oup.com/bioinformatics/article-pdf/28/3/423/16909393/btr670.pdf

Reference8 articles.

1. Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization;Boeva;Bioinformatics,2011

2. High-risk neuroblastoma tumors with 11q-deletion display a poor prognostic, chromosome instability phenotype with later onset;Caren;Proc. Natl Acad. Sci. USA,2010

3. Hallmarks of cancer: the next generation;Hanahan;Cell,2011

4. Catching change-points with lasso;Harchaoui;Adv. Neural Inform. Process. Syst.,2008

5. Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays;Popova;Genome Biol.,2009

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