-
Acquisition_of_additional_mutations_drives_accelerated_progression_of_NPM1_positive_CMML_to_AML_
Study
EGAS00001000619
-
ICGC Oesophageal adenocarcinoma - normal samples
Study
EGAS00001000723
-
Deciphering Developmental Disorders (DDD)
Study
EGAS00001000775
-
Spatial heterogeneity in medulloblastoma
Study
EGAS00001001014
-
Targeted sequencing of 12 genes in patients with HLH
Study
EGAS00001001605
-
Profiling_molecular_heterogeneity_in_human_primary_microglia
Study
EGAS00001002494
-
Combination_Immune_Checkpoint_Inhibition_in_Australian_Rare_Cancers_WES
Study
EGAS00001005709
-
A mechanistic classification of clinical phenotypes in neuroblastoma
Study
EGAS00001003244
-
Application of high-throughput, high-depth, targeted single-nucleus DNA sequencing in pancreatic cancer
Study
EGAS00001006024
-
The impact of mutational clonality in predicting the response to anti-PD-L1/PD-L1 in advanced urothelial cancer
Study
EGAS00001007086
-
Beacon v2
Documentation
about/projects-and-funders/beacon
-
Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling
Dataset
EGAD00001000669
-
Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling
Dataset
EGAD00001000974
-
Transcriptome Changes in ASD (NRXN1α+/-) iPSC-derived neurons
Study
EGAS00001005536
-
WGS and WTS data of patients diagnosed with MEITL.
Dataset
EGAD00001005341
-
Determining genome-wide binding of ETS2 by CUT&RUN in primary human macrophages
Dataset
EGAD00001011349
-
Sensitive and robust liquid biopsy-based detection of PIK3CA mutations
Study
EGAS00001004940
-
Copy Number Arrays
Dataset
EGAD00010001581
-
28 RNA-Seq from CAF-S1, CAF-S4 and EPCAM cells coming from Primary tumors and Lymph nodes of 5 patients)
Dataset
EGAD00001005744
-
PE-META-CENTRAL_ASIA-FETAL
Dataset
EGAD00010001987
-
Transcriptome sequencing of FFPE and patient-derived cultures
Dataset
EGAD50000000246
-
Small RNA sequencing dataset from human prefrontal cortex tissue - ALS vs CTR
Dataset
EGAD50000000468
-
University of Hull
Dac
EGAC50000000402
-
Point-of-care monitoring of head and neck cancer treatment response and recurrence development using nanopore-based ctDNA consensus sequencing
Study
EGAS00001007090
-
Genomic and epigenomic sequencing data on human samples of Institut Curie.
Dac
EGAC50000000356
-
Multiple_myeloma_precursor_genomics
Study
EGAS00001006312
-
Colorectal_organoids_and_tumour_tissue___Whole_Genome_X10
Study
EGAS00001001100
-
Clear cell sarcoma sequencing data
Study
EGAS00001006072
-
ADAPTeR Study: WES data from ccRCC patients
Study
EGAS00001005638
-
Illumina HiSeq 2000
Dataset
EGAD00001003438
-
RNA-Seq Pair End
Dataset
EGAD00001003429
-
Cancer-associated genome-wide hypomethylation and copy number aberrations
Dataset
EGAD00001001093
-
ATAC-seq for placental and buffycoat cells.
Dataset
EGAD00001004291
-
CTCF-ChIP-Seq of cohesin-mutated and wildtype adult AMLs
Dataset
EGAD00001011200
-
Uncovering tumor intrinsic and extrinsic factors that regulate hepatocellular carcinoma growth using patient derived xenograft assays
Dataset
EGAD00001005734
-
BAP1 sequence of uveal melanoma and mesothelioma samples
Dataset
EGAD00001002229
-
Genomic Features of Lung Adenocarcinoma from Individuals with <= 10 Pack-Year Smoking History
Study
phs002556
-
Patient-Specific Factors Influence Somatic Variation Patterns in Von Hippel-Lindau Disease Renal Tumors
Study
phs001107
-
High-Throughput RNA Isoform Sequencing using Programmable cDNA Concatenation
Study
phs003200
-
Whole Exome Sequencing of Uveal Melanoma
Study
phs001370
-
Next Generation Mendelian Genetics: Muscle Hypertrophy
Study
phs000541
-
Targeted Long-Read Sequencing of the Ewing Sarcoma 6p25.1 Susceptibility Locus
Study
phs003159
-
Functional Analysis of Genetic Variants in African Americans with Breast Cancer
Study
phs002977
-
The UC San Diego Chronic Lymphocytic Leukemia (CLL) Study
Study
phs000767
-
Germline DNA Methylation Associated with Breast Cancer Predisposition
Study
phs001699
-
Multi-Omic Investigation of Beckwith-Wiedemann Syndrome Wilms Tumor
Study
phs002769
-
Stanford Center for Urologic Genomics: Genomic Analysis of Benign Prostatic Hyperplasia
Study
phs001698
-
The variable genomic landscape during osteosarcoma progression: insights from a longitudinal WGS analysis
Study
EGAS50000000329
-
TSO500 STJAN33, BRAF mutated CUP
Dataset
EGAD50000000689
-
Immune signature of malignant melanoma in pregnancy
Study
EGAS50000000492