-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001009048
-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001010139
-
Cincinnati Children's Hospital Medical Center (CCHMC) - eMERGE Phase IIIA Data
Study
phs001011
-
Sporadic ALS Australia Systems Genomics Consortium (SALSA-SGC)
Study
phs002068
-
Molecular Genetic Studies of Developmental Brain Disorders
Study
phs000455
-
The Melbourne Urological Research Alliance (MURAL) Collection of Patient-Derived Models of Prostate Cancer
Study
phs003369
-
Bulk ATAC data
Dataset
EGAD00001010188
-
The malaria-protective human glycophorin structural variant DUP4 shows somatic mosaicism and association with hemoglobin levels
Study
EGAS00001003239
-
GTestimate: Improving relative gene expression estimation in scRNA-seq using the Good-Turing estimator
Study
EGAS50000000915
-
PLCG1 R707Q mutation is counter selected under targeted therapy in a patient with a hepatic angiosarcoma
Study
EGAS00001001281
-
Single_Cell_Targeted_Sequence_Capture
Study
EGAS00001000435
-
Results of scRNA-seq analysis of a PBMC collected from a male with a mosaic 45,X/48,XYYY karyotype
Dataset
EGAD00001008645
-
Deep intronic homozygous variation in PSMC3 causes a syndromic neurosensory disorder combining deafness and cataract
Study
EGAS00001003942
-
Employing_single_cell_sequencing_for_detection_of_mutational_signatures_reflecting_on_going_mutagenesis_
Study
EGAS00001002679
-
Genomewide detection of cytosine methylation by single molecule real-time sequencing
Study
EGAS00001004642
-
A GWAS meta-analysis on severe acne on a European population of 26,722 individuals
Study
EGAS00001003278
-
Multi-regional tumour biopsies of a RET fusion patient
Study
EGAS00001004023
-
CIDR: Discovery, Biology, and Risk of Inherited Variants in Glioma
Study
phs002250
-
Cabozantinib Response in ETV6-NTRK3 G623R Positive Carcinoma HIPO-021
Study
EGAS00001004494
-
Whole-genome analysis of a healthy man with common trichromatic vision
Study
JGAS000348
-
The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
-
Pyjacker identifies enhancer hijacking events in acute myeloid leukemia including MNX1 activation via deletion 7q
Study
EGAS50000000743
-
Autosomal Recessive PGM3 Mutations Link Glycosylation Defects to Atopy, Immune Deficiency, Autoimmunity, and Neurocognitive Impairment
Study
phs000809
-
Genetic Study on Nephropathy in Type-2 Diabetes
Study
phs000302
-
Rare germline variants in patients with personal and family history of colorectal cancer
Study
EGAS50000000606
-
Single-cell RNA-seq data from metastatic ovarian cancer for quality control study
Study
EGAS00001005066
-
Long-term Impact and Intervention with Micronutrients in Brazil, Parque Universitário, Community-Based Study
Study
phs003175
-
Primary breast cancers and paired brain metastases sequencing study
Study
EGAS00001003173
-
Synthetic data - Genome in a Bottle
Study
EGAS00001005591
-
Optimized Polyepitope Neoantigen DNA Vaccines Elicit Neoantigen-Specific Immune Responses in Preclinical Models and in Clinical Translation
Study
phs002342
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Metastatic Adult Pancreatoblastoma: Multimodal Treatment and Molecular Characterization of a Very Rare Disease (NCT MASTER)
Study
EGAS00001004157
-
Development of Computational Approaches for Cell Hashing in scRNA-Seq
Study
phs002695
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy
Study
phs002826
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Targeted_EMSeq___Development
Study
EGAS00001007202
-
Metaplastic breast cancer in a patient with neurofibromatosis type 1 and somatic loss of heterozygosity
Study
phs001566
-
Molecular Epidemiology of Colorectal Cancer (MECC) Metastasis Study: A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis
Study
phs001045
-
Non-coding mutations drive persistence of a founder pre-leukemic clone which initiates late relapse in T-ALL
Study
EGAS50000000129
-
Copy Number Variation in Congenital Kidney Malformations
Study
phs000565
-
Mutational landscape of renal cell carcinoma with venous tumor thrombus
Study
EGAS00001001950
-
A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Dataset
EGAD00001000149
-
A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy data
Dataset
EGAD00001004314
-
Genome Sequencing Reveals That RAD50 Hypomorphism Results in Enhanced Sensitivity to Checkpoint Kinase Inhibition Combined with Chemotherapy
Study
phs000706
-
Epigenetic landscape of mixed phenotype leukemias
Study
EGAS00001007094
-
CPTAC: Proteogenomic Studies of Ovarian Tumor Responses to Agents Targeting the DNA Damage Response
Study
phs003152
-
snRNA: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000786
-
bulk ATACseq: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000787
-
scATAC: A Cultured Leukemia Stem Cell Model Enables Validation of CDK6 as a Stemness Target Against Acute Myeloid Leukemia
Study
EGAS50000000788