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GenomicsDAC for study Sequencing component for the whole genome methylation analysis in PBMCs and cell subsets pilot study 1733-sc-2013-
Data Access Committee EGAC00001000096
EGAC00001000096 | EGA
GenomicsGencode Exome Pilot
Data Access Committee EGAC00001000001
EGAC00001000001 | EGA
GenomicsAn immune response network associated with blood lipid levels
Genome-wide genotyping was performed on a population-based cohort from the capital region of Finland using the Illumina 610-Quad SNP microarray
EGAS00000000086 | EGA
GenomicsEGAS00001000490-sc-20130516 - samples
DNA methylation has been shown to play a major role in determining cellular phenotype by regulating gene expression. Moreover, dysregulation of differentially methylated genes has been implicated in disease pathogenesis of various conditions including cancer development as well as autoimmune disease...
EGAD00001000394 | EGA
GenomicsSequencing component for the whole genome methylation analysis in PBMCs and cell subsets pilot study
DNA methylation has been shown to play a major role in determining cellular phenotype by regulating gene expression. Moreover, dysregulation of differentially methylated genes has been implicated in disease pathogenesis of various conditions including cancer development as well as autoimmune disease...
EGAS00001000490 | EGA
GenomicsAn evaluation of different strategies for large scale pooled sequencing study design
Second generation sequencing technology has enabled the design of large-scale sequencing experiments in targeted disease-related regions in thousands of cases and controls. Cost implications dictate a pooled DNA sequencing design, evaluation of allele frequency differences based on the resequenced s...
EGAS00001000134 | EGA
GenomicsEGAS00001000386-sc-20130520 - samples
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAD00001000412 | EGA
GenomicsEGAS00001000190-sc-20130520 - samples
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAD00001000407 | EGA
GenomicsParoxysmal neurological disorders
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000048 | EGA
GenomicsParoxysmal Neurological Disorders 2
We are sequencing the exomes of patients with paroxysmal neurological disorders mainly focusing on migraine and epilepsy. Cases are collected from performance sites of members of the International Headache Genetics consortium and EuroEPINOMICS. Most cases have a strong family history. The study samp...
EGAS00001000190 | EGA
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