-
Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks
Study
EGAS00001002571
-
Exome Sequencing of Spanish Patients with rare genetic diseases.
Study
EGAS00001004028
-
Separation, characterization, and identification of individuals from multi-person blood mixtures with single cell transcriptome sequencing and a novel bioinformatics pipeline
Study
EGAS00001006202
-
DNMT3A microcephalic primordial dwarfism RRBS data
Dataset
EGAD00001004472
-
Targeted sequencing
Dataset
EGAD00001007671
-
EATL-II whole-exome sequencing profile
Dataset
EGAD00001002220
-
Exome sequencing in bipolar disorder families
Dataset
EGAD00001004276
-
RNA sequencing of human fetal brain at 7, 9, 12, 15 and 21 gestational weeks
Dataset
EGAD00001003915
-
Public Access Defibrillation Community Trial (PAD)(PAD-BioLINCC)
Study
phs003858
-
WES of der(1;7)(q10;p10)
Dataset
EGAD50000000986