-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma WES
Dataset
EGAD00001014789
-
IκBε deficiency accelerates disease development in chronic lymphocytic leukemia
Dataset
EGAD50000000754
-
Radiotherapy_induced_Sarcoma_exome
Study
EGAS00001000194
-
Melanoma_brain_metastases
Study
EGAS00001002107
-
V2_panel_bait_design_test
Study
EGAS00001001780
-
ENU_HT_29_BRAF_Triple_Therapy_Clones
Study
EGAS00001001778
-
Keratinocyte_CRISPR_screens
Study
EGAS00001002714
-
Bottleneck_Sequencing_Of_Human_Tissue__Wgs_
Study
EGAS00001004066
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-4)
Study
EGAS00001006101
-
Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
-
Exomes of High-risk Prostate cancer
Study
EGAS00001001015
-
EORTC RP1335 SPECTA Lung cancer data
Study
EGAS00001004485
-
Whole genome sequencing of colorectal cancer patients (SG-BULK-1)
Study
EGAS00001006030
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-2)
Study
EGAS00001006039
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-3)
Study
EGAS00001006056
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-5)
Study
EGAS00001006114
-
Myelodysplastic Syndrome Follow Up Series
Dataset
EGAD00001000283
-
Melanoma-Til Study RNAseq
Dataset
EGAD00001000325
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000794
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000850
-
Mutational Signatures of relapse in rectal cancer FFPE samples in the CR07 clinical trial
Dataset
EGAD00001000875
-
Raw sequencing data - Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Dataset
EGAD00001001381
-
Amplicon-based sequencing of drug resistant lung cancer cell lines (2017-07-05)
Dataset
EGAD00001003425
-
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Dataset
EGAD00001006239
-
Dataset for head_and_neck_cancer-EXON
Dataset
EGAD00001008880
-
Dataset for neuroendocrine_adrenal_tumor-WHOLE_GENOME
Dataset
EGAD00001008893
-
WGS of primary mesothelioma cell lines
Dataset
EGAD00001009641
-
CPC-GENE primary prostate benign and tumour tissue Hi-C sequencing reads
Dataset
EGAD00001008024
-
cfMeDIP data for 67 VPC samples
Dataset
EGAD00001008711
-
cfMeDIP data for 72 VPC samples for validation
Dataset
EGAD00001008737
-
comprehensive genetic analysis and database construction for head and neck cancer
Study
JGAS000214
-
Radiotherapy_induced_sarcoma
Study
EGAS00001000138
-
Oesophageal_Adenocarcinoma_Organoid_ATAC
Study
EGAS00001003890
-
Non-coding mutations drive persistence of a founder pre-leukemic clone which initiates late relapse in T-ALL
Study
EGAS50000000129
-
PGDx elio™ plasma resolve assay: targeted sequencing analyses of plasma cfDNA
Dataset
EGAD00001009719
-
Pharmacological improvement of CFTR function rescues airway epithelial homeostasis and host defense in cystic fibrosis children
Study
EGAS50000000128
-
Genetic Factors associated with Conversion from Active Surveillance to Treatment for Prostate Cancer
Study
phs002056
-
Whole Genome Sequencing of Liver Cancers
Study
EGAS00001002408
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738
-
Most HCCs in Taiwan show the mutational signature of aristolochic acid
Study
EGAS00001002301
-
High-resolution structural genomics reveals new therapeutic vulnerabilities in glioblastoma
Study
EGAS00001003493
-
UCSF Pediatric Bithalamic Glioma Genome Project
Study
EGAS00001004033
-
Microbiota 16S sequencing study in NSCLC patients eligible for surgery without neoadjuvant treatment
Study
EGAS00001004728
-
Phase Ib of olaparib and capivasertib
Study
EGAS00001004930
-
Multiregional sequencing of IDH-WT glioblastoma reveals high genetic heterogeneity and a dynamic evolutionary history
Study
EGAS00001005128
-
Multi-omics analysis of serial samples from metastatic TNBC patients on PARP inhibitor monotherapy provide insight into rational PARP inhibitor therapy combinations
Study
EGAS00001005479
-
Persistent Mutation Burden Drives Sustained Anti-Tumor Immune Responses
Study
EGAS00001006660
-
ENOC WGS for the study Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Dataset
EGAD00001003266
-
exploration of biomarkers discriminating squamous cell carcinoma from other lung cancers
Study
JGAS000488
-
Single-cell multi-omics of relapse/refractory multiple myeloma patients (Hipo K08K/H067/K43R)
Study
EGAS00001006538
-
DNA Double Strand Breaks in KMT2A-Rearranged AML patients
Study
phs002804
-
Genomic sequencing of Pediatric Rhabdomyosarcoma
Study
phs000720
-
Genome Sequencing of Hepatocellular Carcinoma at The Human Genome Sequencing Center of Baylor College of Medicine (HGSC-BCM)
Study
phs000509
-
Health Professionals Follow-Up Study
Study
phs002460
-
Whole exome sequencing of tumors from the Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Dataset
EGAD00001010928
-
Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases
Dataset
EGAD00001005197
-
A Genome-Wide Association Study in Patients Experiencing Musculoskeletal Adverse Events on NCIC CTG Trial MA.27 Evaluating Aromatase Inhibitors as Adjuvant Therapy in Early Breast Cancer. A Collaboration Between the NIH Pharmacogenetics Research Network and the RIKEN Yokohama Institute Center for Genomic Medicine.
Study
phs000210
-
Somatic_mutation_and_clonal_evolution_in_the_human_pancreas___WGS
Study
EGAS00001002626
-
Targeted_Sequencing_of_Human_Myeloid_Malignancies
Study
EGAS00001001289
-
Lymphocyte_LCM_WGS
Study
EGAS00001003384
-
Melanoma_post_mortem_analysis
Study
EGAS00001003531
-
_WGS__Somatic_mutation_in_skin_epidermis__SMS_
Study
EGAS00001004464
-
Chondrosarcoma_Targeted_Sequencing_Study
Study
EGAS00001000277
-
A common single nucleotide variant in T is strongly associated with chordoma
Dataset
EGAD00001000226
-
Targeted sequencing of genes recurrently mutated in AML - part2
Dataset
EGAD00001000747
-
TMD-AMKL targeted follow-up part 2
Dataset
EGAD00001000879
-
SOFT study - sequencing premenopausal breast cancer (2017-11-22)
Dataset
EGAD00001003811
-
Adenoma development in familial adenomatous polyposis and MUTYH‐associated polyposis: somatic landscape and driver genes
Dataset
EGAD00001004332
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Dataset
EGAD00001004501
-
WES of blood and patient-matched cecum tumor tissue samples, Panel NGS of patient-matched cfDNA
Dataset
EGAD00001005737
-
Circulating cell-free DNA analyses for Patient Monitoring in Small Cell Lung Cancer
Dataset
EGAD00001007070
-
Development and Validation of a Prognostic and Predictive 32-Gene Signature for Gastric Cancer
Dataset
EGAD00001008091
-
Hubrecht Organoid Technology Colon Cancer Study
Dataset
EGAD00001008445
-
Dataset for hepatopancreaticobiliary_malignancy-EXON
Dataset
EGAD00001008883
-
Dataset for hepatopancreaticobiliary_malignancy-WHOLE_GENOME
Dataset
EGAD00001008884
-
Dataset for urologic_cancer-EXON
Dataset
EGAD00001008904
-
CASCADE low-pass whole genome sequencing data
Dataset
EGAD00001009494
-
PGDx elio plasma resolve analytical validation
Dataset
EGAD00001009718
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 2)
Dataset
EGAD00001009791
-
Tracking early lung cancer metastatic dissemination in TRACERx using ctDNA dataset
Dataset
EGAD00001010031
-
252 human breast cancer samples in WGS and WES
Dataset
EGAD00001007563
-
Amplicon based re-sequencing of multi-region PDAC samples
Dataset
EGAD50000000354
-
CHEK2 molecular manuscript
Study
EGAS50000000080
-
Anti-tumor and Immune Stimulatory Activity of Iberdomide in Myeloma, Including Patients with Cereblon Dysregulation
Study
EGAS50000000265
-
Transcriptome_human_nasal_epithelium
Study
EGAS00001001294
-
Structure and evolution of double minutes in diagnosis and relapse brain tumors
Study
EGAS00001003212
-
Exome sequencing
Study
EGAS00001005761
-
Innate myeloid cell sbuset-specific gene expression patterns in the human colon are altered in Crohn's disease patients
Study
JGAS000127
-
Gene expression of human Th17 cells before and after activation
Study
JGAS000005
-
DNA demethylation is associated with malignant progression of low-grade gliomas
Study
JGAS000146
-
Longitudinal_profiling_of_the_immune_response_to_Plasmodium_vivax_in_naive_hosts_by_RNA_sequencing
Study
EGAS00001003847
-
Systemic Lupus Erythematosus Serum Stimulation of Human Intestinal Organoids Induces Barrier Leakiness and Changes in Goblet Cell Differentiation
Study
EGAS50000000012
-
Carboxylesterase 1 mediates a distinctive metabolic profile of dendritic cells to attain an inflammatory phenotype
Study
EGAS50000000230
-
Parallel CRISPR Editing of Familial ALS Mutations Into a Healthy Control iPSC Line
Study
phs002440
-
Transposable Elements in FTLD-TDP and ALS-TDP
Study
phs001889
-
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Study
phs002031
-
Non-Coding Autoimmune Risk Variant Defines Role for ICOS in T Peripheral Helper Cell Development
Study
phs003448
-
Blood DNA Methylation in Post-Acute Sequelae of COVID-19 (PASC): a Prospective Cohort Study
Study
phs003658
-
Healthy_ageing_thymus
Study
EGAS00001004311
-
Natural Killer Cell Therapies for Hematologic Malignancies
Study
phs002681