Barillot E - Search Results

1

Application of Atlas of Cancer Signalling Network in preclinical studies.

Monraz Gomez LC, Kondratova M, Ravel JM, Barillot E, Zinovyev A, Kuperstein I. Monraz Gomez LC, et al. Among authors: barillot e. Brief Bioinform. 2019 Mar 25;20(2):701-716. doi: 10.1093/bib/bby031. Brief Bioinform. 2019. PMID: 29726961 Review.

2

VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles.

La Rosa P, Viara E, Hupé P, Pierron G, Liva S, Neuvial P, Brito I, Lair S, Servant N, Robine N, Manié E, Brennetot C, Janoueix-Lerosey I, Raynal V, Gruel N, Rouveirol C, Stransky N, Stern MH, Delattre O, Aurias A, Radvanyi F, Barillot E. La Rosa P, et al. Among authors: barillot e. Bioinformatics. 2006 Sep 1;22(17):2066-73. doi: 10.1093/bioinformatics/btl359. Epub 2006 Jul 4. Bioinformatics. 2006. PMID: 16820431

3

ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays.

Rigaill G, Hupé P, Almeida A, La Rosa P, Meyniel JP, Decraene C, Barillot E. Rigaill G, et al. Among authors: barillot e. Bioinformatics. 2008 Mar 15;24(6):768-74. doi: 10.1093/bioinformatics/btn048. Epub 2008 Feb 5. Bioinformatics. 2008. PMID: 18252739

4

Classification of arrayCGH data using fused SVM.

Rapaport F, Barillot E, Vert JP. Rapaport F, et al. Among authors: barillot e. Bioinformatics. 2008 Jul 1;24(13):i375-82. doi: 10.1093/bioinformatics/btn188. Bioinformatics. 2008. PMID: 18586737 Free PMC article.

5

[Systems biology of cancer].

Barillot E, Calzone L, Zinovyev A. Barillot E, et al. Med Sci (Paris). 2009 Jun-Jul;25(6-7):601-7. doi: 10.1051/medsci/2009256-7601. Med Sci (Paris). 2009. PMID: 19602357 Free article. French.

6

SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data.

Zeitouni B, Boeva V, Janoueix-Lerosey I, Loeillet S, Legoix-né P, Nicolas A, Delattre O, Barillot E. Zeitouni B, et al. Among authors: barillot e. Bioinformatics. 2010 Aug 1;26(15):1895-6. doi: 10.1093/bioinformatics/btq293. Bioinformatics. 2010. PMID: 20639544 Free PMC article.

7

Girafe--an R/Bioconductor package for functional exploration of aligned next-generation sequencing reads.

Toedling J, Ciaudo C, Voinnet O, Heard E, Barillot E. Toedling J, et al. Among authors: barillot e. Bioinformatics. 2010 Nov 15;26(22):2902-3. doi: 10.1093/bioinformatics/btq531. Epub 2010 Sep 21. Bioinformatics. 2010. PMID: 20861030 Free PMC article.

8

Control-free calling of copy number alterations in deep-sequencing data using GC-content normalization.

Boeva V, Zinovyev A, Bleakley K, Vert JP, Janoueix-Lerosey I, Delattre O, Barillot E. Boeva V, et al. Among authors: barillot e. Bioinformatics. 2011 Jan 15;27(2):268-9. doi: 10.1093/bioinformatics/btq635. Epub 2010 Nov 15. Bioinformatics. 2011. PMID: 21081509 Free PMC article.

9

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

Boeva V, Popova T, Bleakley K, Chiche P, Cappo J, Schleiermacher G, Janoueix-Lerosey I, Delattre O, Barillot E. Boeva V, et al. Among authors: barillot e. Bioinformatics. 2012 Feb 1;28(3):423-5. doi: 10.1093/bioinformatics/btr670. Epub 2011 Dec 6. Bioinformatics. 2012. PMID: 22155870 Free PMC article.

10

Nebula--a web-server for advanced ChIP-seq data analysis.

Boeva V, Lermine A, Barette C, Guillouf C, Barillot E. Boeva V, et al. Among authors: barillot e. Bioinformatics. 2012 Oct 1;28(19):2517-9. doi: 10.1093/bioinformatics/bts463. Epub 2012 Jul 24. Bioinformatics. 2012. PMID: 22829625

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