-
High-coverage whole exome sequence in non-TRU-type lung adenocarcinomas
Study
JGAS000105
-
DEPArray-based sorting of pure carcinoma and stromal populations from formalin-fixed paraffin-embedded (FFPE) tissues followed by targeted sequencing
Study
EGAS50000001327
-
A single-cell multi-omic atlas of nodal B-cell non-Hodgkin lymphomas
Study
EGAS50000000342
-
Non-Mendalian inheritance of extrachromosal DNA elements can drive disease evolution in glioblastoma
Study
EGAS00001001878
-
Exome_sequencing_of_thyroid_disease_in_Val_Borbera
Study
EGAS00001000344
-
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors
Study
EGAS00001000906
-
Frequent somatic transfer of mitochondrial DNA into the nuclear genome of human cancer cells
Study
EGAS00001001234
-
A collection of 142 samples used to evaluate the sensitivity and specificity of small-scale variation detection in exome-capture data with a particular focus on indel detection.
Study
EGAS00001001332
-
Chromosome Y Philogeny in Sardinia
Study
EGAS00001000532
-
Relaxed selection during a recent human expansion
Study
EGAS00001001957
-
The KATHERINE study of adjuvant trastuzumab emtansine in HER2-positive breast cancer: analysis of patients with HER2-negative residual invasive disease on re-testing
Study
EGAS00001006037
-
Tumor-associated preferred end coordinates and somatic variants as signatures of circulating tumor DNA
Study
EGAS00001003160
-
Genome-wide expression profiles to compare array-based, RNAseq and NanoString technologies in patients with resected pancreatic ductal carcinoma.
Study
EGAS00001002501
-
Whole exome sequencing in RVOT patients
Study
EGAS00001002319
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET)
Study
EGAS00001003813
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
RNA-seq of Glioblastoma stem cells
Study
EGAS00001003070
-
UAMS Smoldering Myeloma Timeline Cohort
Study
EGAS00001003687
-
Phase Ib of olaparib and capivasertib
Study
EGAS00001004930
-
Longitudinal_Cambridge_Study_COVID19
Study
EGAS00001004488
-
Assessment of the Toll-like receptor 3 response in hepatocytes
Study
EGAS00001005147
-
Single_cell_HSC_colony_WGS_many_years_post_allogeneic_bone_marrow_transplant
Study
EGAS00001003744
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
Study
EGAS00001002632
-
Multiple migrations to the Philippines during the last 50,000 years
Study
EGAS00001005083
-
Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Study
EGAS00001004277
-
Egyptref: An integrated personal and population-based Egyptian genome reference
Study
EGAS00001004303
-
The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas
Study
EGAS00001003787
-
Profiling_heterogeneity_in_Human_derived_IPSC_neurons
Study
EGAS00001002885
-
Peripheral immunoprofiling of stratifies COVID-19 patients based on disease-specific neutrophil signatures
Study
EGAS00001004503
-
Germline variant analysis in childhood AML
Study
EGAS00001006276
-
Pathogenic variants damage cell compositions and single cell transcription in cardiomyopathies
Study
EGAS00001006374
-
Single-cell multi-omics of relapse/refractory multiple myeloma patients (Hipo K08K/H067/K43R)
Study
EGAS00001006538
-
Longitudinal monitoring of cell-free DNA methylation in ALK-positive non-small cell lung cancer patients
Study
EGAS00001006573
-
Profiling of childhood neuroblastoma and the immune microenvironment by single-cell sequencing of RNA and TCR
Study
EGAS00001006823
-
GCparagon: Evaluation and correction of GC biases in cell-free DNA at the fragment level
Study
EGAS00001006963
-
Facial Skin Biophysical Multi-Parameter and Microbiome-Based Korean Skin Cutoype (KSC) Determination
Study
EGAS00001007334
-
Whole Exome sequencing of colorectal cancer patients (SG-BULK)
Dataset
EGAD00001008543
-
Activation of Wnt/β-catenin signalling by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary gland basal cell adenoma - RNA
Dataset
EGAD00001015366
-
Activation of Wnt/β-catenin signalling by mutually exclusive FBXW11 and CTNNB1 hotspot mutations drives salivary gland basal cell adenoma - WES
Dataset
EGAD00001015365
-
Smith-Lemli-Opitz Syndrome: A Longitudinal Clinical Study of Patients Receiving Cholesterol Supplementation
Study
phs001430
-
The Human Virome in Children and its Relationship to Febrile Illness
Study
phs000264
-
Coagulation and Fibrinolysis in a Pediatric Insulin Titration Trial
Study
phs003016
-
Acute Respiratory Distress Network (ARDSNet) Study 04 Assessment of Low Tidal Volume and Elevated End-Expiratory Volume to Obviate Lung Injury (ALVEOLI-BioLINCC)
Study
phs003714
-
SC_DDD-G-4
Dataset
EGAD00010001604
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs)
Dataset
EGAD50000000138
-
Genome-Wide Scan for Genetic Variants Associated with Early-Onset Prostate Cancer
Study
phs001185
-
Single cell chromatin accessibility profiles from myelofibrosis patients
Dataset
EGAD50000000234
-
FASTQ Data from In Situ Hi-C on Medulloblastoma Tissue Samples
Dataset
EGAD50000000771
-
PanelSeq IDC samples
Dataset
EGAD50000001149