SNPs3D: candidate gene and SNP selection for association studies, BMC Bioinformatics, vol.7, issue.1, pp.166-166, 2006. ,
DOI : 10.1186/1471-2105-7-166
FunctSNP: an R package to link SNPs to functional knowledge and dbAutoMaker: a suite of Perl scripts to build SNP databases, BMC Bioinformatics, vol.11, issue.1, p.311, 2010. ,
DOI : 10.1186/1471-2105-11-311
SNP Function Portal: a web database for exploring the function implication of SNP alleles, Bioinformatics, vol.22, issue.14, pp.523-529, 2006. ,
DOI : 10.1093/bioinformatics/btl241
SNPit: A federated data integration system for the purpose of functional SNP annotation, Computer Methods and Programs in Biomedicine, vol.95, issue.2, pp.181-189, 2009. ,
DOI : 10.1016/j.cmpb.2009.02.010
LS-SNP/PDB: annotated non-synonymous SNPs mapped to Protein Data Bank structures, Bioinformatics, vol.25, issue.11, pp.1431-1432, 2009. ,
DOI : 10.1093/bioinformatics/btp242
URL : http://bioinformatics.oxfordjournals.org/cgi/content/short/25/11/1431
A SNP-centric database for the investigation of the human genome, BMC Bioinformatics, vol.5, issue.1, p.33, 2004. ,
DOI : 10.1186/1471-2105-5-33
SNPeffect v2.0: a new step in investigating the molecular phenotypic effects of human non-synonymous SNPs, Bioinformatics, vol.22, issue.17, pp.2183-2185, 2006. ,
DOI : 10.1093/bioinformatics/btl348
Snap: an integrated SNP annotation platform, Nucleic Acids Research, vol.35, issue.Database, pp.707-710, 2007. ,
DOI : 10.1093/nar/gkl969
URL : http://doi.org/10.1093/nar/gkl969
BioMart Central Portal--unified access to biological data, Nucleic Acids Research, vol.37, issue.Web Server, pp.23-27, 2009. ,
DOI : 10.1093/nar/gkp265
URL : http://doi.org/10.1093/nar/gkp265
Narcisse: a mirror view of conserved syntenies, Nucleic Acids Research, vol.36, issue.Database, pp.485-490, 2008. ,
DOI : 10.1093/nar/gkm805
BioMAJ: a flexible framework for databanks synchronization and processing, Bioinformatics, vol.24, issue.16, pp.1823-1825, 2008. ,
DOI : 10.1093/bioinformatics/btn325
URL : https://hal.archives-ouvertes.fr/inria-00327502
The mh gene causing double-muscling in cattle maps to bovine Chromosome 2, Mammalian Genome, vol.3, issue.11, pp.788-792, 1995. ,
DOI : 10.1007/BF00539005
A deletion in the bovine myostatin gene causes the double???muscled phenotype in cattle, Nature Genetics, vol.18, issue.1, pp.71-74, 1997. ,
DOI : 10.1006/geno.1993.1465
Mapping quantitative trait loci affecting fatness and breast muscle weight in meat-type chicken lines divergently selected on abdominal fatness, Genetics Selection Evolution, vol.38, issue.1, pp.85-97, 2006. ,
DOI : 10.1186/1297-9686-38-1-85
URL : https://hal.archives-ouvertes.fr/hal-00894553
A comprehensive analysis of QTL for abdominal fat and breast muscle weights on chicken chromosome 5 using a multivariate approach, Animal Genetics, vol.10, issue.Suppl. 2, pp.157-164, 2009. ,
DOI : 10.1111/j.1365-2052.2008.01817.x
URL : https://hal.archives-ouvertes.fr/hal-00729933
A factor model to analyze heterogeneity in gene expression, BMC Bioinformatics, vol.11, issue.1, p.368, 2010. ,
DOI : 10.1186/1471-2105-11-368
URL : https://hal.archives-ouvertes.fr/hal-00729426
Using transcriptome profiling to characterize QTL regions on chicken chromosome 5, BMC Genomics, vol.10, issue.1, p.575, 2009. ,
DOI : 10.1186/1471-2164-10-575
URL : https://hal.archives-ouvertes.fr/hal-00730106
Trait correlated expression combined with expression QTL analysis reveals biological pathways and candidate genes affecting water holding capacity of muscle, BMC Genomics, vol.9, issue.1, p.367, 2008. ,
DOI : 10.1186/1471-2164-9-367
Genetic validation of whole-transcriptome sequencing for mapping expression affected by cis-regulatory variation, BMC Genomics, vol.11, issue.1, p.473, 2010. ,
DOI : 10.1186/1471-2164-11-473
Diversification in the genetic architecture of gene expression and transcriptional networks in organ differentiation of Populus, Proc. Natl Acad. Sci. USA, pp.8492-8497, 2010. ,
DOI : 10.1073/pnas.0914709107
Expression Quantitative Trait Loci: Replication, Tissue- and Sex-Specificity in Mice, Genetics, vol.185, issue.3, pp.1059-1068, 2010. ,
DOI : 10.1534/genetics.110.116087