GSM637405[Accession] - GEO DataSets

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Items: 4

Select item 2000261061.

Genetic identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.

Organism:: Homo sapiens

Type:: Expression profiling by array; SNP genotyping by SNP array; Genome variation profiling by SNP array

Platforms:: GPL4133 GPL8887 GPL6104
748 Samples

Download data: TXT

Series

Accession:: GSE26106

ID:: 200026106

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 2000259352.

Genetic identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue [Agilent]

(Submitter supplied) Most loci identified in genome wide association studies (GWAS) of complex traits reside in non-coding DNA and may contribute to phenotype via changes in gene regulation. The discovery of expression quantitative trait loci (‘eQTLs’) can thus be used to more precisely identify modest but real disease associations and provide insights into their underlying molecular mechanisms. This is particularly true for analyses of expression in non-transformed cells from tissues relevant to the complex traits of interest. more...

Organism:: Homo sapiens

Type:: Expression profiling by array

Platform:: GPL4133
464 Samples

Download data: TXT

Series

Accession:: GSE25935

ID:: 200025935

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000041333.

Agilent-014850 Whole Human Genome Microarray 4x44K G4112F (Feature Number version)

(Submitter supplied) This multi-pack (4X44K) formatted microarray represents a compiled view of the human genome as it is understood today. The sequence information used to design this product was derived from a broad survey of well known sources such as RefSeq, Goldenpath, Ensembl, Unigene and others. The resulting view of the human genome covers 41K unique genes and transcripts which have been verified and optimized by alignment to the human genome assembly and by Agilent's Empirical Validation process. more...