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GenomicsCardiogenics_24K - samples
Cambridge control samples using a 24k expression array from Illumina
EGAD00010000389 | EGA
GenomicsCardiogenics_660K - samples
Cambridge control samples using a 660K genotyping chip from Illumina
EGAD00010000391 | EGA
GenomicsCardiogenics_1.2M - samples
Cambridge control samples using a 1.2M genotyping chip from Illumina
EGAD00010000387 | EGA
GenomicsPowerful Identification of Cis-regulatory SNPs in Human Primary Monocytes Using Allele-Specific Gene Expression
The aim of this study was to compare the power to detect associations between SNPs using cis-eQTL mapping and ASE analysis (allele specific expression).
EGAS00000000119 | EGA
GenomicsASE vs GTE Study Data Access Committee
Data Access Committee EGAC01000000019
EGAC01000000019 | EGA
TranscriptomicsTranscription profiling of differentiated human blood cells: The HaemAtlas
Transcription profiling of highly purified blood cells from normal individuals
ORGANISM(S): Homo sapiens 
2009-02-06 | E-TABM-633 | biostudies-arrayexpress
Genomicsena-DATASET-UCAM-GEL-15-04-2015-15:15:23:555-345 - samples
Whole exome sequencing BAM files for samples from the BRIDGE Consortium with pathogenic or likely pathogenic variants on genes linked to bleeding or platelet disorders.
EGAD00001001333 | EGA
GenomicsSequencing of heritable Bleeding and Platelet Disorders
The BRIDGE-BPD study aims to discover new causal genes for Bleeding and Platelet Disorders (BPD) by high throughput sequencing using cluster analyses based on improved and standardized deep phenotyping of cases. BPD is one of the 13 Rare Disease projects under the NIHR BioResource Rare Diseases BRID...
EGAS00001001172 | EGA
GenomicsNIHR BioResource DAC
Data Access Committee EGAC00001000259
EGAC00001000259 | EGA
GenomicsATD
WTCCC1 project Autoimmune Thyroid Disease (ATD) samples
EGAD00000000011 | EGA
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