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Dataset for synovial_sarcoma-WHOLE_GENOME
Dataset
EGAD00001008899
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Epilepsy related sudden death (2019-08-21)
Dataset
EGAD00001005276
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Single-cell RNA-Seq (Chromium Next GEM Single Cell 3' Reagent Kits v3.1 from 10X Genomics )
Dataset
EGAD00001010907
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scRNA-seq
Dataset
EGAD00001011139
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RNA-seq dataset of CD34+ HSPCs from LRMDS patients
Dataset
EGAD00001015771
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Target capture sequence for Primary-recurrent HCC study
Dataset
EGAD00001005450
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The National Institute of Neurological Disorders and Stroke (NINDS) Stroke Genetics Network (SiGN)
Study
phs000615
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Defective Homologous Recombination DNA Repair as Therapeutic Target in Advanced-Stage Chordoma (HIPO_021)
Study
EGAS00001002720
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Resuscitation Outcomes Consortium (ROC) Prehospital Resuscitation Using an Impedance Valve and Early Versus Delayed Analysis (PRIMED) (ROC-PRIMED-BioLINCC)
Study
phs003825
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OncoArray: Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Study
phs001882
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5- FU treated organoids
Study
EGAS00001003592
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Loss of LGR4/GPR48 causes severe neonatal salt-wasting due to disrupted WNT signaling altering adrenal zonation
Study
EGAS00001006808
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CYP2C19 long-read sequencing
Study
EGAS00001006929
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Transcriptional consequences of SETBP1 variants in developmental disorders and malignancies
Dataset
EGAD00001015482
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Identification of Targetable FGFR Gene Fusions in Diverse Cancers
Study
phs000602
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IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
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deCODE Genetics study on genes contributing to nicotine dependence in humans
Study
phs000393
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NIDDK⁄CIDR Inflammatory Bowel Disease Genetics Consortium (IBDGC) Genome Wide Association Study in Familial Crohn's Disease
Study
phs000367
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Clonal heterogeneity leads to secondary resistance in a melanoma patient after adoptive cell therapy with tumor-infiltrating lymphocytes
Study
EGAS50000000279
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Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
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Pathogenic variants damage cell compositions and single cell transcription in cardiomyopathies
Study
EGAS00001006374
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Confirmation of a founder effect in a Northern European population (FRL) of a new beta-globin variant: HBB:c.23_26dup (codons 8/9 (+AGAA))
Study
EGAS00001000980
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A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients
Study
EGAS00001004491
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KIR gene content imputation from single-nucleotide polymorphisms in the Finnish population
Study
EGAS00001005457
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EWS-WT1 Fusion Isoforms Establish Oncogenic Programs and Therapeutic Vulnerabilities in Desmoplastic Small Round Cell Tumors
Study
phs003682