WorldCat Identities

Bardel, Claire

Overview
Works: 12 works in 13 publications in 2 languages and 23 library holdings
Roles: Other, Author, Contributor
Publication Timeline
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Most widely held works by Claire Bardel
Mise en évidence de facteurs génétiques de risque en utilisant des phylogénies d'haplotypes by Claire Bardel( Book )

2 editions published in 2005 in French and held by 3 WorldCat member libraries worldwide

Impact of Interleukin-6 on Drug-Metabolizing Enzymes and Transporters in Intestinal Cells by Florian Simon( )

1 edition published in 2019 in English and held by 2 WorldCat member libraries worldwide

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers by Breast Cancer Family Registry( )

1 edition published in 2015 in English and held by 2 WorldCat member libraries worldwide

Dealing with missing phase and missing data in phylogeny-based analysis by Claire Bardel( )

1 edition published in 2007 in English and held by 2 WorldCat member libraries worldwide

Familial vs. sporadic sarcoidosis: BTNL2 polymorphisms, clinical presentations, and outcomes in a French cohort by GSF group( )

1 edition published in 2016 in English and held by 2 WorldCat member libraries worldwide

Whole exome sequencing in three families segregating a pediatric case of sarcoidosis by In the frame of GSF (Groupe Sarcoïdose France)( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

Efficiency of multiple imputation to test for association in the presence of missing data by Pascal Croiseau( )

1 edition published in 2007 in English and held by 2 WorldCat member libraries worldwide

Transcriptional regulation of CRMP5 controls neurite outgrowth through Sox5 by Nicolas Naudet( )

1 edition published in 2017 in English and held by 2 WorldCat member libraries worldwide

A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus by Lenha Mobuchon( )

1 edition published in 2017 in English and held by 2 WorldCat member libraries worldwide

On the use of haplotype phylogeny to detect disease susceptibility loci by Claire Bardel( )

1 edition published in 2005 in English and held by 2 WorldCat member libraries worldwide

Centralization errors in comparative genomic hybridization array analysis of pituitary tumor samples( )

1 edition published in 2018 in English and held by 1 WorldCat member library worldwide

Abstract: Reliable interpretation of comparative genomic hybridization array (aCGH) results requires centralization and normalization of the data. We evaluated the reliability of aCGH centralization by comparing aCGH results (with classical centralization-normalization steps) to fluorescence in situ hybridization (FISH) results. In addition, we propose a method to correct centralization bias. Sixty-six pituitary tumors were analyzed (Agilent aCGH + SNP 4 × 180K microarray). For each tumor, the FISH-based log2 (ratios) of a subset of chromosomes were compared with the corresponding aCGH raw log2 (ratios). With our new normalization-centralization process, this difference was added to all log2 (ratios), before performing loess regression on non-altered probes only. Finally, the mean log2 (ratio) and the percentage of normal probes were compared between CGHnormaliter and our new FISH-based method. For 11 tumors, FISH results and raw CGH log2 (ratios) differed significantly. In addition, nine tumors showed discrepancies between results generated by CGHnormaliter and our new-method. Such discrepancies seemed to occur with tumours with many abnormalities (0%-40% normal probes), rather than in those tumours with fewer abnormalities (31%-100% normal probes). Five tumors had too few normal probes to allow normalization. In these tumors, which can exhibit many changes in DNA copy number, we found that centralization bias was frequent and uncorrected by current normalization methods. Therefore, an external control for centralization, such as FISH analysis, is required to insure reliable interpretation of aCGH data
Utilisation de phylogénies d'haplotypes pour la mise en évidence de facteurs génétiques de risque dans les maladies complexes by Claire Bardel( Book )

1 edition published in 2002 in French and held by 1 WorldCat member library worldwide

 
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Languages
English (10)

French (3)