-
Type I Interferon Exacerbates Mycobacterium Tuberculosis Induced Human Macrophage Death
Study
phs003607
-
The Genomic Landscape of Mongolian Hepatocellular Carcinoma
Study
phs002000
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
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
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Study
EGAS00001004093
-
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
-
Myelodysplastic_syndrome_whole_genomes
Study
EGAS00001000291
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR_Custom
Study
EGAS00001002257
-
Precursor_lesions__clonal_architecture_and_relapse_in_Wilms_nephroblastoma
Study
EGAS00001001422
-
Myeloproliferative_Disease_Whole_Genomes
Study
EGAS00001000290
-
Molecular analysis of circulating tumour cells identifies distinct profiles in chemosensitive and chemorefractory patients with small cell lung cancer
Study
EGAS00001001951
-
Genome-wide search for higher order epistasis as modifiers of treatment effects on bone mineral density in childhood cancer survivors
Study
EGAS00001002645
-
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Study
EGAS00001004507
-
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
-
A practical guide for mutational signature analysis in hematological malignancies
Dataset
EGAD00001005028
-
Dataset for soft_tissue_tumor-EXON
Dataset
EGAD00001008897
-
Comparison of single/pooled CTCs and bulk exome sequencing
Dataset
EGAD00001009052
-
Shallow Whole Genome Sequencing of Patient Derived Xenografts
Dataset
EGAD50000000277
-
Other NS tumors
Dataset
EGAD50000000299
-
Establishment of an integrated database for clinical and genomic data in cancer
Study
JGAS000206
-
Melanoma PEACE Dataset
Dataset
EGAD00001010877
-
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
Study
EGAS50000000021
-
Transcriptional_analysis_of_cells_from_lungs
Study
EGAS00001002649
-
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
-
(Epi)genetic Risk Architectures of Opioid-Dependent Brain
Study
phs002724
-
The cellular immune and airway epithelial profile throughout childhood and in response to COVID-19 at multi-omic single cell level.
Dataset
EGAD00001007718
-
Lactobacillus rhamnosus GG ATCC (LGG) as an immune adjuvant for influenza vaccination in the elderly
Study
phs000981
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Whole-Genome and Epigenomic Landscapes of Etiologically Distinct Subtypes of Cholangiocarcinoma
Study
EGAS00001001653
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
Comparison of 133/144bp dominant phenotype vs 166bp dominant phenotype.
Study
EGAS00001004135
-
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
-
Structural variant analysis of homologous recombination-deficient genomes
Study
EGAS00001007186
-
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
-
Molecular analysis of post-colonoscopy CRC (PCCRC)
Study
EGAS00001004686