Published in Nucleic Acids Res on November 04, 2013
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Rapid phenotyping of knockout mice to identify genetic determinants of bone strength. J Endocrinol (2016) 0.75
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Temporally and Spatially Regulated Expression of the Linker Histone H1fx During Mouse Development. J Histochem Cytochem (2017) 0.75
Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis. Nat Genet (2017) 0.75
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Promoting coherent minimum reporting guidelines for biological and biomedical investigations: the MIBBI project. Nat Biotechnol (2008) 12.96
Optimized design and assessment of whole genome tiling arrays. Bioinformatics (2007) 11.38
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A standard variation file format for human genome sequences. Genome Biol (2010) 7.83
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ArrayExpress update--an archive of microarray and high-throughput sequencing-based functional genomics experiments. Nucleic Acids Res (2010) 7.67
A simple spreadsheet-based, MIAME-supportive format for microarray data: MAGE-TAB. BMC Bioinformatics (2006) 7.53
Five-vertebrate ChIP-seq reveals the evolutionary dynamics of transcription factor binding. Science (2010) 7.41
The MGED Ontology: a resource for semantics-based description of microarray experiments. Bioinformatics (2006) 7.37
EGASP: the human ENCODE Genome Annotation Assessment Project. Genome Biol (2006) 7.06
Using ontologies to describe mouse phenotypes. Genome Biol (2004) 7.03
Molecular maps of the reorganization of genome-nuclear lamina interactions during differentiation. Mol Cell (2010) 6.71
Modeling sample variables with an Experimental Factor Ontology. Bioinformatics (2010) 6.27
A promoter-level mammalian expression atlas. Nature (2014) 6.25
Ensembl BioMarts: a hub for data retrieval across taxonomic space. Database (Oxford) (2011) 6.04
The genome of a songbird. Nature (2010) 5.90
Genome analysis of the platypus reveals unique signatures of evolution. Nature (2008) 5.74
The landscape of histone modifications across 1% of the human genome in five human cell lines. Genome Res (2007) 5.67
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucleic Acids Res (2013) 5.66
De novo assembly and genotyping of variants using colored de Bruijn graphs. Nat Genet (2012) 5.61
eVOC: a controlled vocabulary for unifying gene expression data. Genome Res (2003) 5.41
Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis. PLoS Biol (2010) 5.39
Modeling biomedical experimental processes with OBI. J Biomed Semantics (2010) 5.36
A global map of human gene expression. Nat Biotechnol (2010) 5.32
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Modernizing reference genome assemblies. PLoS Biol (2011) 5.23
Genome-wide nucleotide-level mammalian ancestor reconstruction. Genome Res (2008) 5.12
Gene expression atlas at the European bioinformatics institute. Nucleic Acids Res (2009) 4.99
ArrayExpress update--trends in database growth and links to data analysis tools. Nucleic Acids Res (2012) 4.91
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs). Genome Res (2008) 4.84
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The functional spectrum of low-frequency coding variation. Genome Biol (2011) 4.42
Locus Reference Genomic sequences: an improved basis for describing human DNA variants. Genome Med (2010) 4.19
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Insights into hominid evolution from the gorilla genome sequence. Nature (2012) 4.12
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Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets. Genome Res (2008) 4.08
A public gene trap resource for mouse functional genomics. Nat Genet (2004) 3.96
Public data archives for genomic structural variation. Nat Genet (2010) 3.92
A CTCF-independent role for cohesin in tissue-specific transcription. Genome Res (2010) 3.89
The otter annotation system. Genome Res (2004) 3.88
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ArrayExpress service for reviewers/editors of DNA microarray papers. Nat Biotechnol (2006) 3.61
Gene Expression Atlas update--a value-added database of microarray and sequencing-based functional genomics experiments. Nucleic Acids Res (2011) 3.61
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Matrix-insensitive protein assays push the limits of biosensors in medicine. Nat Med (2009) 3.58
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The International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouse. Nucleic Acids Res (2006) 3.40
Dynein mutations impair autophagic clearance of aggregate-prone proteins. Nat Genet (2005) 3.39
Circadian orchestration of the hepatic proteome. Curr Biol (2006) 3.37
Multiplex protein assays based on real-time magnetic nanotag sensing. Proc Natl Acad Sci U S A (2008) 3.34
The European Bioinformatics Institute's data resources. Nucleic Acids Res (2003) 3.34
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. Curr Biol (2003) 3.31
BLUEPRINT to decode the epigenetic signature written in blood. Nat Biotechnol (2012) 3.24
The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium. Nucleic Acids Res (2010) 3.23
The DNA sequence of human chromosome 7. Nature (2003) 3.18
FlyBase: improvements to the bibliography. Nucleic Acids Res (2012) 3.17
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TranscriptSNPView: a genome-wide catalog of mouse coding variation. Nat Genet (2006) 3.10
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell (2007) 3.06
The BioSample Database (BioSD) at the European Bioinformatics Institute. Nucleic Acids Res (2011) 3.05
BioMart Central Portal: an open database network for the biological community. Database (Oxford) (2011) 3.03
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nat Genet (2003) 2.98