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Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015378
-
Exploring the driver events of eccrine poromas and porocarcinomas: A retrospective, cross-institutional study of 90 cases
Dataset
EGAD00001015379
-
RNA-Sequencing and Somatic Mutation Status of Adrenocortical Tumors: Novel Pathogenetic Insights
Study
EGAS00001004533
-
GA4GH
Documentation
about/projects-and-funders/ga4gh
-
Bone Microarchitecture
Study
phs002102
-
Direct Transposition of Native DNA for Sensitive Multimodal Single-Molecule Sequencing
Study
phs003511
-
Novel regional age-associated DNA methylation changes within human common disease-associated loci
Study
EGAS00001001910
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
NIH Roadmap Epigenomics Program - Broad Institute
Study
phs000700
-
Melanoma_TIL_Study_Exomes
Study
EGAS00001000216
-
Barcelona_kids_with_melanoma
Study
EGAS00001000733
-
Whole Exome Sequencing of 15 Tumor/Normal pairs of inflammatory hepatocellular adenomas
Study
EGAS00001003686
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Study
EGAS00001000714
-
MYD88/TLR mutations in CLL
Study
EGAS00001000772
-
Comprehensive investigation of genome architecture of gastric adenocarcinoma with whole-genome sequencing in the Chinese population.
Study
EGAS00001002404
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 1).
Study
EGAS00001002630
-
Mutational spectrum of highly differentiated, fusion-negative rhabdomyosarcoma (set 2).
Study
EGAS00001002771
-
Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
-
High-resolution lung adenocarcinoma expression subtypes identify tumors with dependencies on MET, CDK4, CDK6, and PD-L1
Study
EGAS00001006461
-
Tissue DNA, WBC DNA and cfDNA (deep-)sequencing of mCRC patients treated with doublet chemotherapy and anti-EGFR in the CAIRO5 study
Study
EGAS00001006695
-
Targeted Sequencing of 173 genes
Dataset
EGAD00001002115
-
Undifferentiated sarcomas develop through distinct evolutionary pathways
Dataset
EGAD00001004162
-
The landscape of somatic mutation in normal colorectal epithelial cells
Dataset
EGAD00001004193
-
Metabolic reprogramming towards OXPHOS identifies a novel therapeutic target for mantle cell lymphoma
Dataset
EGAD00001004577
-
A compendium of mutational signatures due to environmental exposures
Dataset
EGAD00001004583
-
Direct transcriptional consequences of somatic mutation in breast cancer
Dataset
EGAD00001002237
-
Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Dataset
EGAD00001002651
-
Enrichment of homologous recombination repair alteration in prostate cancer brain metastases
Dataset
EGAD00001008033
-
Eribulin efficacy in platinum-resistant and refractory high-grade serous ovarian cancer patient-derived xenograft models
Study
EGAS50000000152
-
Whole exome sequencing and methylation profiling of uveal melanoma
Study
phs001421
-
Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab on NSABP B-40
Study
phs001365
-
RB1 Loss Triggers Dependence on ESRRG in Retinoblastoma
Study
phs002859
-
APOLLO1: Proteogenomic Analysis of Lung Adenocarcinoma
Study
phs003011
-
Evolution of Chronic Lymphocytic Leukemia to Richter's Syndrome (RS)
Study
phs002458
-
Whole Genome Sequencing of HER2-Positive Metastatic Extramammary Paget’s Disease: A Case Report
Study
EGAS50000000243
-
Diagnosis of pediatric central nervous system tumors using methylation profiling of cfDNA from cerebrospinal fluid
Study
EGAS50000000377
-
DIAMOND PCR : plasma DNA LINE-1 targeted bisulfite sequencing, a new non-invasive multi-cancer detection marker
Dataset
EGAD50000000646
-
Characterization of copy number quiet oral cancer
Study
EGAS50000000558
-
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Study
EGAS00001000160
-
NGS_based_viability_screening_using_haploid_cell_line
Study
EGAS00001001095
-
MPN_TGS2_Follow_up___PT1_Vori_other
Study
EGAS00001000765
-
Exploring_the_landscape_of_somatic_mutations_in_normal_tissue___GI___MAP___WGS
Study
EGAS00001004122
-
To determine the genomic profile of Triple Negative Breast Cancer patient-derived xenografts (PDX cohort)
Study
EGAS00001005995
-
Whole genome sequence of liver cancers displaying biliary phenotype
Dataset
EGAD00001000809
-
Whole genome sequencing of RIKEN liver cancers
Dataset
EGAD00001001642
-
Genomic alteration in Korean Young Age Diffuse Gastric Cancers
Dataset
EGAD00001001984
-
Ovarian cancer/normal cell lines
Dataset
EGAD00001003146
-
CancerSEEK ctDNA FASTQ files
Dataset
EGAD00001003931
-
Whole Genome Sequencing for Korean Diffuse Gastric Cancer
Dataset
EGAD00001003953
-
whole-genome sequencing of gastric cancer
Dataset
EGAD00001004811
-
TONIC study Whole Exome Sequencing
Dataset
EGAD00001004857
-
Combination Therapies for Personalised Cancer Medicine in 11-18 (2019-06-10)
Dataset
EGAD00001005081
-
Immunopeptidomics of colorectal cancer organoids reveals a sparse HLA class I neoantigen landscape and no increase in neoantigens with interferon or MEK-inhibitor treatment
Dataset
EGAD00001005357
-
Synchronous Colorectal Cancer genome sequencing
Dataset
EGAD00001006131
-
Pre and Post BCG treated bulk RNAseq dataset.
Dataset
EGAD00001006634
-
Dataset for liposarcoma-EXON
Dataset
EGAD00001008886
-
Dataset for NSCLC-EXON
Dataset
EGAD00001008892
-
10x Genomics Single Cell Gene Expression for SA1035X5XB03021
Dataset
EGAD00001009153
-
Single Cell Genome Sequence for DLP+ library A95618B
Dataset
EGAD00001009316
-
Single Cell Genome Sequence for DLP+ library A96130A
Dataset
EGAD00001009454
-
Single Cell Genome Sequence for DLP+ library A96161A
Dataset
EGAD00001009457
-
Single Cell Genome Sequence for DLP+ library A96173A
Dataset
EGAD00001009459
-
Single Cell Genome Sequence for DLP+ library A96175A
Dataset
EGAD00001009461
-
Single Cell Genome Sequence for DLP+ library A96177C
Dataset
EGAD00001009462
-
Single Cell Genome Sequence for DLP+ library A96180A
Dataset
EGAD00001009463
-
WGS data of colorectal cancer patients
Dataset
EGAD00001007746
-
Single Cell Genome Sequence for DLP+ library A96141A
Dataset
EGAD00001009513
-
Bone marrow single cell genomics from blood cancer samples
Dataset
EGAD00001011055
-
multi-region sequencing of tumor samples from PDAC patients
Dataset
EGAD00001011109
-
Long-read methylation analysis of breast cancer using the enzymatic base conversion and the nanopore sequencing
Study
JGAS000265
-
Homopolymer switches WES dataset
Dataset
EGAD50000000319
-
The_Little_Princess_Knowledge_Bank_
Study
EGAS00001004237
-
Whole-genome sequencing of high-retrotransposition rate tumours
Study
EGAS50000000414
-
Spatial and temporal diversity in genomic instability processes define early stage lung cancer evolution.
Study
EGAS00001000840
-
Whole genome characterisation of lung cancer organoids and tissue
Study
EGAS00001002899
-
The genomic and radiomic complexity of multifocal prostate cancer
Study
EGAS00001002767
-
TRACERx: TRAcking non-small cell lung Cancer Evolution through therapy (Rx). Pilot Study. Multi-region sequencing of early-stage NSCLCs.
Study
EGAS00001000809
-
Capture Hi-C identifies the chromatin interactome of colorectal cancer risk loci
Study
EGAS00001001085
-
Evolutionary analysis of pancreatic cancer and coexistent precursor lesions using whole exome sequencing data
Study
EGAS00001002778
-
HGSC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003268
-
cfDNA and CDX/PDX methylation profiling in Small Cell Lung Cancer
Dataset
EGAD00001008673
-
The Two Sister Study: A Family-Based Study of Genes and Environment in Young-Onset Breast Cancer
Study
phs000678
-
Comparative Sequence Analysis Between Primary and Metastatic Colorectal Cancer Lesions
Study
phs000790
-
Gabriella Miller Kids First Pediatric Research Program in Genetics at the Intersection of Childhood Cancer and Birth Defects
Study
phs001846
-
Molecular Basis of Neuroendocrine Prostate Cancer (Trento/Cornell/Broad 2015)
Study
phs000909
-
Genomic Tumor Correlates of Clinical Outcomes Following Organ-Sparing Chemoradiation Therapy for Bladder Cancer
Study
phs003402
-
Genomic landscape of oral cancers (Illumina RNA-Seq)
Study
EGAS00001003237
-
PD-L1 blockade in combination with carboplatin as immune induction in metastatic lobular breast cancer: the GELATO-trial
Study
EGAS00001006902
-
A higher ctDNA fraction decreases survival in regorafenib-treated metastatic colorectal cancer patients
Study
EGAS00001004491
-
Detection of ctDNA in Plasma of Patients with Clinically Localised Prostate Cancer is Associated with Rapid Disease Progression
Study
EGAS00001004636
-
Colorectal cancer study
Study
EGAS00001006489
-
Follow-up of Ovarian Cancer Genetic Association and Interaction Studies (FOCI)
Study
phs001133
-
Clonal fitness inferred from timeseries modeling of single cell cancer genomes
Study
EGAS00001004448
-
Circulating tumor DNA dynamics reveal KRAS G12C mutation heterogeneity and response to treatment with the KRAS G12C inhibitor divarasib in solid tumors
Study
EGAS50000000315
-
RNA Expression in Diverse Donor Derived Dermal Fibroblasts Correlates with Reprogramming to Pluripotency
Study
phs002341
-
Targeted bisulfite sequencing
Dataset
EGAD00001004785
-
COVID-19 Severity First Wave of Infection for Severe Patients in Madrid
Dataset
EGAD00001008464
-
Single cell targeted DNA-sequencing (and antibody sequencing) of high hyperdiploid B-ALL
Dataset
EGAD50000000829
-
scDNA-seq for 'Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma'
Dataset
EGAD00001015414
-
MPN_mutation_order_followup
Study
EGAS00001000663