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GenomicsCodelink_HWG_CLD_B
Codelink Human Whole Genome from Blood taken at 72 hours after birht
EGAD00010001424 | EGA
GenomicsCodelink_HWG_noCLD_CB
Codelink Human Whole Genome from Blood taken at 72 hours after birht
EGAD00010001425 | EGA
GenomicsTranscriptome analysis in very preterm infants with chronic lung disease after birth
Bronchopulmonary dysplasia (BPD) is the most common complication of prematurity and is characterized by impaired alveolar and vascular development. The aim of the study was to identify early BPD-relevant pathways by applying whole genome transcriptional profiling combined with protein measurements f...
EGAS00001002586 | EGA
GenomicsDAC for Transcriptome analysis in very preterm infants with chronic lung disease after birth
Data Access Committee EGAC00001000698
EGAC00001000698 | EGA
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
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