-
Guardians of the genome: protecting DNA from endogenous sources of damage
Dataset
EGAD00001006055
-
Prediction of HLA genotypes using NGS data
Dataset
EGAD00001007733
-
Spatial transcriptome sequence data from cross section of cancer containing prostates
Dataset
EGAD00001008644
-
Ither2 WXS dataset - Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Dataset
EGAD00001010178
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 6)
Dataset
EGAD00001010202
-
Whole exome and targeted DNA sequencing data for formalin-fixed paraffin embedded tissue from de novo small cell prostatic carcinoma cases
Dataset
EGAD00001004139
-
Chromosome Segregation Errors Promote a Diverse Spectrum of Simple and Complex Genomic Rearrangements
Dataset
EGAD00001004163
-
IMMUcan SCCHN1 cohort
Study
EGAS50000001533
-
L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population
Study
phs000732
-
scRNA-seq of LN and lymphoma stroma
Study
EGAS00001005732
-
The Genomic Landscape of Mongolian Hepatocellular Carcinoma
Study
phs002000
-
Single-cell profiling reveals mechanisms of response to anti-PD-L1 versus anti-PD-L1 combined with anti-CTLA4 in head and neck squamous cell carcinoma
Study
EGAS50000000037
-
Germ Cell and Associated Heme Malignancies Evolve from a Common Shared Precursor
Study
phs002231
-
The Spatio-Temporal Evolution of Multiple Myeloma from Baseline to Relapse-Refractory States
Study
phs002625
-
GATA2 Deficiency
Study
phs002311
-
Integrated Genomic Analysis of Periampullary Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000895
-
Tandem DNA Repeats Activate hTERT Gene Transcription
Study
phs002428
-
Pre-Existing Skin-Resident CD8 and γδ T Cell Circuits Mediate Immune Response in Merkel Cell Carcinoma and Predict Immunotherapy Efficacy
Study
phs003629
-
Exome sequencing identifies mutation of the ribosome in T-cell acute lymphoblastic leukemia
Study
EGAS00001000296
-
Finding the way towards the eradication of therapy-related myeloid neoplasms
Blog
eradication-of-therapy-related-myeloid-neoplasms
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Study
EGAS00001004093
-
Inhibiton of the GABPB1L-containing GABP tetramer is sufficient to reverse replicative immortality in TERT promoter mutant glioblastoma cells.
Study
EGAS00001002582
-
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
-
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
-
St. Jude Children’s Research Hospital – Washington University Pediatric Cancer Genome Project Steering Committee
Dac
EGAC00001000044
-
Somatic mutations, clonal architecture and genomic evolution in multiple myeloma
Dataset
EGAD00001000339
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Dataset
EGAD50000000277
-
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Study
EGAS50000000021
-
Other NS tumors
Dataset
EGAD50000000299
-
Genome-wide NanoRCS of cfDNA from plasma of healthy individuals
Study
EGAS50000000695
-
Childhood B-cell acute lymphoblastic leukemia genomic and transcriptomic data
Study
EGAS00001006863
-
Clonal evolution of metastatic colorectal cancer under anticancer therapies
Study
EGAS50000001023
-
Establishment of an integrated database for clinical and genomic data in cancer
Study
JGAS000206
-
16S rRNA gene V4 region sequencing data, ASV profiles, and sample metadata of human faecal samples predominantly from the Estonian population
Dataset
EGAD50000002306
-
A New CA19-9 Cut-Off Value Identifies Lewis Antigen Status and Refines Prognostic Stratification in PDAC
Study
EGAS50000001575
-
Impact of Mutated CTCF DNA binding sites of Topologically associating domains on nearby Cancer Gene Regulation: A Multi-Omics Analysis
Study
EGAS50000001686
-
Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer
Study
EGAS00001001951
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors
Study
EGAS00001002645
-
Myelodysplastic_syndrome_whole_genomes
Study
EGAS00001000291
-
Myeloproliferative_Disease_Whole_Genomes
Study
EGAS00001000290
-
Transcriptional_analysis_of_cells_from_lungs
Study
EGAS00001002649
-
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Study
EGAS00001004507
-
Comparison of single/pooled CTCs and bulk exome sequencing
Dataset
EGAD00001009052
-
A developmental cell atlas of the human thyroid gland - WGS
Dataset
EGAD00001015447
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015455
-
Dataset for soft_tissue_tumor-EXON
Dataset
EGAD00001008897
-
DERMATLAS: Hidradenoma papilliferum_RNAseq
Dataset
EGAD00001015480
-
NEOPREDICT-Lung: longitudinal whole exome sequencing of non-small cell lung cancers under immunotherapy
Dataset
EGAD00001015362
-
Sebaceous carcinoma tumor/normal exome sequencing and transcriptome sequencing. Transcriptome sequencing of
Dataset
EGAD00001004016
-
A practical guide for mutational signature analysis in hematological malignancies
Dataset
EGAD00001005028
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015457
-
DERMATLAS: Hidradenoma papilliferum_WES
Dataset
EGAD00001015481
-
Melanoma PEACE Dataset
Dataset
EGAD00001010877
-
Somatic mutation in edited cholangiocyte organoids
Dataset
EGAD00001015456
-
(Epi)genetic Risk Architectures of Opioid-Dependent Brain
Study
phs002724
-
Type I Interferon Exacerbates Mycobacterium Tuberculosis Induced Human Macrophage Death
Study
phs003607
-
Understanding human fetal pancreas development using subpopulation sorting and RNA sequencing
Study
EGAS00001003127
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma_CM67-RNASeq
Dataset
EGAD00001006306
-
MGHBoston_Molpheno_Closed
Dataset
EGAD00001004866
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM066-WES
Dataset
EGAD00001006309
-
The cellular immune and airway epithelial profile throughout childhood and in response to COVID-19 at multi-omic single cell level.
Dataset
EGAD00001007718
-
Genetics of Chemotherapy Induced Peripheral Neuropathy in N08C1 and N08CB
Study
phs001480
-
North Carolina Clinical Genomic Evaluation by NextGen Exome Sequencing (NCGENES)
Study
phs000827
-
Drug screening of patient-derived organoids from colorectal peritoneal metastases
Study
phs002023
-
Transformation of Dysplasia in Barrett's Esophagus
Study
phs002706
-
Germline Genetics of Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML)
Study
phs002962
-
Rituximab-treated lymphoma patients show correlated deficiency in serological and T cell Spike-specific response after SARS-CoV-2 vaccination: insights from the CORSA Study.
Study
EGAS50000001205
-
Transposable Elements Shape Stemness in Normal and Leukemic Hematopoiesis
Study
EGAS50000001141
-
Transposable Elements Shape Stemness in Normal and Leukemic Hematopoiesis
Study
EGAS50000001147
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Enrichment of oral-derived bacteria in inflamed colorectal tumors and distinct associations of Fusobacterium in the mesenchymal subtype
Study
EGAS00001006757
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Study
EGAS00001004135
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
Molecular analysis of post-colonoscopy CRC (PCCRC)
Study
EGAS00001004686
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
Genomic gain of EBV's LMP-1 in NKTCL
Study
EGAS50000000260
-
Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK)
Study
phs001271
-
Targeted capture, whole genome sequencing, and RNAseq to identify rearrangements in B-cell lymphomas
Study
EGAS50000000328
-
Comprehensive genetic landscape, immune checkpoint profiling, and establishment of patient-derived xenograft (PDX) of metachronous brain tumors from constitutive mismatch repair deficiency with a biallelic variant on MSH6
Study
EGAS50000000351
-
Spatial predictors of response to immunotherapy in microsatellite stable metastatic colorectal cancer
Dataset
EGAD50000002244
-
Primary breast tumor heterogeneity through therapy
Study
EGAS00001003168
-
WXS of 147 lung cancer patients treated with immunotherapy
Study
EGAS00001003781
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Study
EGAS00001002132
-
Unraveling metastatic progression of breast cancer
Study
EGAS00001000760
-
NRG1 Fusions in KRAS Wild-type Pancreatic Cancer (H021)
Study
EGAS00001002759
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
-
Panbody_nanoseq
Study
EGAS00001005521
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015259
-
Somatic mutant selection is altered by prior NOTCH1 mutation in ageing esophageal epithelium
Dataset
EGAD00001015260
-
Whole exome sequencing of endometriod ovarian cancer tumours
Dataset
EGAD00001006389
-
The Precision Medicine in Liver Cancer across an Asia-pacific NETwork (PLANET) - Intratumoural immune heterogeneity
Dataset
EGAD00001006570
-
Single-cell gene expression data from CD8+ T cells from two Austrian COVID19 patients stimulated with wildtype and mutant SARS-Cov-2 peptides
Dataset
EGAD00001006995
-
Dataset for the Pearl study
Dataset
EGAD00001007979