-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
NHGRI GREGoR Consortium: Genomics Research to Elucidate the Genetics of Rare Disease
Study
phs003047
-
A genotype-phenotype study of tumors from patients with inherited mutations in DNA repair genes
Study
phs003348
-
SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
-
Comprehensive characterization of cell-free tumor DNA in plasma and urine of patients with renal tumors
Study
EGAS00001003530
-
Distinct portrayal of lesions in synchronous multifocal lung adenocarcinoma revealed by genome sequencing
Study
EGAS00001001572
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
Study
EGAS00001002538
-
SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Study
EGAS00001002920
-
Low and variable tumor reactivity of the intratumoral TCR repertoire in human cancers
Study
EGAS00001003119
-
Whole genome sequencing of Ewings Sarcoma
Study
EGAS00001003385
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
Target gene sequencing for human normal endometrial glands
Study
EGAS00001005914
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001006306
-
Detection of Genes Predisposing to Hematologic Malignancies
Study
phs001219
-
The Genomic Landscape of Endocrine Resistant Advanced Breast Cancers: Paired Pre- and Post-endocrine Therapy Samples.
Study
phs001674
-
Characterizing TP53 and PPM1D Mutations as Resistance Drivers to Radiation Therapy in Diffuse Intrinsic Pontine Gliomas
Study
phs002380
-
High response rate to anti PD-1 therapy in desmoplastic melanoma
Study
phs001469
-
Cohort-Based Genome-Wide Association Study of Glioma (GliomaScan)
Study
phs000652
-
Altered chromosomal topology drives oncogenic programs in gastrointestinal stromal tumors
Study
phs001906
-
Whole Genome Association Study of Systemic Lupus Erythematosus
Study
phs000122
-
Germline Genetics of Myelodysplastic Syndromes (MDS) and Acute Myeloid Leukemia (AML)
Study
phs002962
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
Prediction of homologous recombination deficiency identifies colorectal tumors sensitive to PARP inhibition
Study
EGAS50000000426
-
scRNA-seq of LN and lymphoma stroma
Study
EGAS00001005732
-
L1-Seq and Genome-Wide SNP Genotyping in a Multiethnic Asian Population
Study
phs000732
-
Functional Significance of Prostate Cancer Risk-SNPs
Study
phs000985
-
Amplicon_based_sequencing_of_drug_resistant_organoids
Study
EGAS00001001639
-
ENU_LS_411N_TripleTherapy
Study
EGAS00001001777
-
Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000812
-
RNAseq___Discovery_of_resistance_mechanisms_to_the_BRAF_inhibitor_vemurafenib_in_metastatic_BRAF_mutant_melanoma
Study
EGAS00001000813
-
Mutational_burden_in_human_hair_follicles
Study
EGAS00001004462
-
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+)
Study
EGAS00001005078
-
Whole genome analyses of the childhood cancer neuroblastoma
Dataset
EGAD00001000282
-
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
-
Guardians of the genome: protecting DNA from endogenous sources of damage
Dataset
EGAD00001006055
-
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
-
Prediction of HLA genotypes using NGS data
Dataset
EGAD00001007733
-
The chemotherapeutic CX-5461 is extremely mutagenic and may increase cancer risk
Study
EGAS50000000023
-
Childhood Cancer Data Initiative (CCDI): CCDI Pediatric In Vivo Testing Program - Leukemia
Study
phs003164
-
Ballett
Study
EGAS50000000478
-
Catalog Statistics
Documentation
about/statistics/catalog
-
Multi-omics data of 1000 Inflammatory Bowel Disease patients
Study
EGAS00001002702
-
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_CM67-RNASeq
Dataset
EGAD00001006306
-
Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma - CM066-WES
Dataset
EGAD00001006309
-
Understanding human fetal pancreas development using subpopulation sorting and RNA sequencing
Study
EGAS00001003127