-
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
-
Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
-
Longitudinal evaluation of serum microRNAs as biomarkers for neuroblastoma burden and therapeutic p53 reactivation
Study
EGAS00001006678
-
Stratifying and Targeting Pediatric Medulloblastoma through Genomics
Study
EGAS00001000273
-
Establishment of an integrated database for clinical and genomic data in cancer
Study
JGAS000206
-
Impact of Mutated CTCF DNA binding sites of Topologically associating domains on nearby Cancer Gene Regulation: A Multi-Omics Analysis
Study
EGAS50000001686
-
Clonal evolution of metastatic colorectal cancer under anticancer therapies
Study
EGAS50000001023
-
Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer
Study
EGAS00001001951
-
A New CA19-9 Cut-Off Value Identifies Lewis Antigen Status and Refines Prognostic Stratification in PDAC
Study
EGAS50000001575
-
NIBIT-EPI-MESO study samples
Study
EGAS50000001478
-
Whole Exome sequencing of colorectal cancer patients (SG-BULK)
Study
EGAS00001006006
-
RNA seq data of 2 lung cancer samples prepared using 2 different RNA-seq library preparation protocols
Study
EGAS50000001419
-
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
-
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Study
EGAS50000000021
-
Single-cell targeted DNA-sequencing and protein sequencing
Study
EGAS50000000580
-
Genome-wide NanoRCS of cfDNA from plasma of healthy individuals
Study
EGAS50000000695
-
Childhood B-cell acute lymphoblastic leukemia genomic and transcriptomic data
Study
EGAS00001006863
-
Molecular correlates for HPV-negative head and neck cancer engraftment prognosticate patient outcomes
Study
EGAS50000000714
-
RNA-seq data from 121 tumor samples with muscle invasive bladder cancer.
Study
EGAS00001004505
-
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
-
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
-
An Advanced Molecular Medicine Case Report of a Rare Human Tumor Using Genomics, Pathomics, and Radiomics
Study
phs003154
-
Immune Responses in Checkpoint Myocarditis Across Heart, Blood, and Tumor
Study
phs003413
-
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
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Transposable Elements Shape Stemness in Normal and Leukemic Hematopoiesis
Study
EGAS50000001141
-
Transposable Elements Shape Stemness in Normal and Leukemic Hematopoiesis
Study
EGAS50000001147
-
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
-
mFAST-SeqS
Study
EGAS00001001133
-
Molecular analysis of post-colonoscopy CRC (PCCRC)
Study
EGAS00001004686
-
Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
-
BMP4 and temozolomide synergize in the majority of patient derived glioblastoma cultures
Study
EGAS00001007095
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
Genomic gain of EBV's LMP-1 in NKTCL
Study
EGAS50000000260
-
Pooled Genome-Wide Analysis of Kidney Cancer Risk (KIDRISK)
Study
phs001271
-
Whole exome sequencing and RNA sequencing of cervical cancer
Study
JGAS000586
-
Whole exome sequencing and RNA sequencing of cervical cancer
Study
JGAS000582