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TranscriptomicsGenotyping data from 54 patients with deficit schizophrenia
Schizophrenia is a severe psychiatric disease with complex etiology, affecting approximately one percent of the general population. Most genetic studies so far focused on disease association with common genetic variation such as single nucleotide polymorphisms, but recently it has become apparent th...
ORGANISM(S): Homo sapiens 
2010-05-18 | E-GEOD-12714 | biostudies-arrayexpress
GenomicsBenchmark and validation of whole exome sequencing of a trio and singleton
Whole exome paired-end sequencing data was obtained for a trio and a fourth unrelated individual sequenced to high depth (95x) using a paired-end library with the Illumina HiSeq platform and aligned by BWA 0.5.9. The bam files were analysed and experimentally vaidated for the novel insertion of mobi...
EGAS00001000852 | EGA
Genomicsena-DATASET-RUNMC-17-07-2014-15:19:55:636-69 - samples
Illumina HiSeq paired-end exome sequencing of a trio and singleton.
EGAD00001000883 | EGA
TranscriptomicsNuclear receptors Nur77 and Nurr1 modulate mesenchymal stromal cell migration
Expression analysis of migrating and non-migrating mesenchymal stromal cells (MSC) in fetal bone marrow Keywords: fetal bone marrow, mesenchymal stromal cells, migration, gene expression, genomics Three biological replates for both migrating and non-migrating mesenchymal stromal cells (MSC) in feta...
ORGANISM(S): Homo sapiens 
2011-10-23 | E-GEOD-24892 | biostudies-arrayexpress
GenomicsWhole genome DNA sequencing for two long-lived humans.
Two long-lived human samples were sequenced to a mean 20x coverage genome wide. Sequencing was done using the Illumina hi-seq platform, alignment to GRCh37/hg19 reference genome was done using the BWA alignment tool.
EGAS00001000877 | EGA
GenomicsLLS_2SAMPLES_DATASET - samples
Description not provided
EGAD00001001001 | EGA
GenomicsDepartment of Human Genetics, Radboud University Nijmegen Medical Centre, Data Access Committee
Data Access Committee EGAC00001000076
EGAC00001000076 | EGA
GenomicsLeiden Longevity Study Data Access Committee
Data Access Committee EGAC00001000210
EGAC00001000210 | EGA
GenomicsGenome-wide profiling of p63 binding sites identifies genes and regulatory elements for p63-related disorders
We identified p63 target genes and binding sites responsible for ectodermal defects by genome-wide profiling of p63 binding using ChIP-seq and expression analysis in human primary keratinocytes from patients with p63 mutations. As proof of principle, we identified a novel de novo microdeletion causi...
ORGANISM(S): Homo sapiens 
2010-08-15 | E-GEOD-17611 | biostudies-arrayexpress
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