-
scEC&T-seq manuscript data
Dataset
EGAD00001010071
-
Digital tEchnology For Lung Cancer Treatment
Study
EGAS00001007219
-
Genome-Wide Association of Type 2 Diabetes in Africans: The AADM Study
Study
phs001844
-
ACTIV-6: COVID-19 Outpatient Randomized Trial to Evaluate Efficacy of Repurposed Medications
Study
phs003941
-
Phenotype Risk Scores Identify Patients with Unrecognized Mendelian Disease Patterns
Study
phs001516
-
Alpha1-Antitrypsin Deficiency Registry (AADR-BioLINCC)
Study
phs004187
-
DAC for BillionToOne
Dac
EGAC50000000418
-
APL nanopore sequencing
Study
EGAS00001005618
-
Transdisciplinary Studies of Genetic Variation in Colorectal Cancer(CORECT): Axiom GWAS
Study
phs001856
-
A Genomic Approach to Improved Diagnosis and Treatment of Neuroendocrine Tumors
Study
phs001772
-
Comprehensive analysis of the abnormality of the genes in juvenile myelomonocytic leukemia
Study
JGAS000292
-
RNA004 Nanopore DRS of peripheral blood
Study
EGAS50000001201
-
Single cell RNA sequencing of co-culture of human organoids with polarized pro-inflammatory (M1) or anti-inflammatory (M2) macrophages
Study
EGAS50000000467
-
Single-nucleus transcriptome sequencing of the ALS-FTD motor cortex after sorting by TDP-43
Study
EGAS50000001566
-
Integrative and comparative genomic analyses identify clinically relevant groups of pulmonary carcinoids and unveil the supra-carcinoids
Study
EGAS00001003699
-
Genome-wide association data on male-pattern baldness
Study
EGAS00001001354
-
June 2017 data update (bam/fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001003414
-
SCLC study MGH - WES dataset
Dataset
EGAD00001003970
-
June 2018 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001004300
-
ATAC-seq data in normal colon mucosa
Study
EGAS00001005281
-
Synthetic genotypes and phenotypes of 500.000 individuals
Study
EGAS00001006552
-
Fastq files used for searching for variants associated with endometriosis at 9p21 region
Dataset
EGAD00001001942
-
September 2016 data update (bam/fastq/vcf) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001002724
-
May 2019 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001005060
-
August 2019 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001005335
-
August 2020 data update (fastq) for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001006383
-
KiCS cancer panel data for academic and for-profit use
Dataset
EGAD00001009734
-
Genetic determinants of monocyte splicing are enriched for disease susceptibility loci including for COVID-19
Dataset
EGAD00001010176
-
Drug Signatures for Prediction and Mitigation of Toxicity
Study
phs002088
-
Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
CATHeterization GENetics (CATHGEN)
Study
phs000703
-
Fixation effects on variant-calling in a clinical resequencing panel
Study
EGAS00001003507
-
single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes
Study
EGAS00001004070
-
Deep amplicon sequencing to infer malignant clonal populations for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003986
-
Exploring germline and somatic mutagenesis in the extended family with germline pathogenic variant in POLD1
Study
EGAS00001006434
-
Towards standardized whole exome sequencing (WES) for cancer patients: lessons from a multicentric pilot study
Study
EGAS00001007363
-
This study generated Oxford Nanopore long read sequencing data of cancer cell line mixtures for validating long-read variant calls in cancer genomics
Study
EGAS00001008107
-
The data access committee for "Validation of cfDNA fragmentome analyses for early detection of liver cancer"
Dac
EGAC00001003543
-
Medulloblastoma WES
Study
EGAS50000000261
-
Deep_sequencing_of_melanoma_for_driver_mutations
Study
EGAS00001000857
-
Elucidating Mechanisms of the Graft versus Leukemia Effect of Hematopoietic Stem Cell Transplant for Acute Myeloid Leukemia
Study
phs003630
-
Single-cell transcriptome analysis of B-cell development in the ABO platform
Dataset
EGAD50000002433
-
Normal brain controls for ICGC PedBrain DNA methylation sequencing
Study
EGAS00001000909
-
March 2019 data update for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001004950
-
DAC for study CMMRD–associated high-grade glioma
Dac
EGAC50000000855
-
Long-read whole genome sequencing as a tool for variant detection in inherited retinal dystrophies
Study
EGAS50000000846
-
Whole Genome Sequencing for Korean Diffuse Gastric Cancer
Dataset
EGAD00001003953
-
The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Dataset
EGAD00001006335
-
Hyperpolarized carbon-13 MRI for very early response assessment of neoadjuvant chemotherapy in breast cancer patients
Dataset
EGAD00001008141
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004