-
MicroRNA profiling by next-generation sequencing for colorectal cancer screening
Study
EGAS00001005030
-
DERMATLAS__Hidradenoma_papilliferum_RNAseq
Study
EGAS00001005715
-
Somatic mutations in endometriosis and normal uterine endometrium
Study
EGAS00001003095
-
DERMATLAS__Porocarcinoma_RNAseq
Study
EGAS00001005721
-
Germline elongator mutations in sonic hedgehog medulloblastoma
Study
EGAS00001004126
-
Cancer immune control needs senescence induction by Stat1 dependent cell cycle regulator pathways in tumours
Study
EGAS00001004151
-
FAM50A_Disruption_in_TOV21G_Cells___RNAseq
Study
EGAS00001004156
-
The WID-BC-index identifies women with primary poor prognostic breast cancer based on DNA methylation in cervical samples
Study
EGAS00001005055
-
Molecular_risk_stratification_in_patients_with_T1_colorectal_cancer_WES
Study
EGAS00001005734
-
Automated image-based profiling of complex drug induced phenotypes in patient-derived organoids
Study
EGAS00001003140
-
Panbody_nanoseq
Study
EGAS00001005521
-
'KOREAN' never-smoker female adenocarcinoma RNA-seq
Study
EGAS00001003789
-
Subtype specific studies of breast cancer progression. Milan cohort.
Study
EGAS00001004390
-
The WID-CIN test identifies women with, and at risk of, cervical intraepithelial neoplasia grade 3 and invasive cervical cancer (CIN3+)
Study
EGAS00001005078
-
Detection of Cancer Mutations by Urine Liquid Biopsy in Bladder Cancer Patients
Study
EGAS00001005758
-
CRISPR transduction of iPS cells
Study
EGAS00001005102
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
Persistence of circulating tumor DNA in breast cancer patients during neoadjuvant treatment is a significant predictor of poor tumor response
Study
EGAS00001005798
-
Single_cell_resolution_of_human_CNV_body_map
Study
EGAS00001003162
-
Sequencing of cancer autopsies and ctDNA
Study
EGAS00001005109
-
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Study
EGAS00001005572
-
Genomics to select patients with metastatic breast cancer for targeted therapy (microarray_cytoscan)
Study
EGAS00001005584
-
A living biobank of breast cancer organoids captures disease heterogeneity
Study
EGAS00001002158
-
Somatic_mutation_in_skin_epidermis__SMS_
Study
EGAS00001002165
-
Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
-
Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
-
Whole-exome sequencing of ovarian clear cell carcinoma in clinical outliers
Study
EGAS00001004248
-
Chemotherapy accelerates genomic aging of normal blood in children treated for cancer
Study
EGAS00001005141
-
Molecular origins of mpMRI visibility
Study
EGAS00001003179
-
Targeted sequencing of paired tumour/blood of 34 T1 stage bladder cancer patients
Study
EGAS00001005767
-
Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer
Study
EGAS00001005769
-
arrayCGH for copy number profiling on tumor DNA from pediatric cancer tissue samples
Study
EGAS00001005197
-
The_identification_of_genetic_vulnerabilities_in_head_and_neck_cancers_for_the_development_of_novel_therapies
Study
EGAS00001002204
-
Ductal keratin 15+ luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
Study
EGAS00001005963
-
Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
-
MethCORR: DNA Methylation-based Characterization, Classification and Prognostication of Colorectal Cancer using Archival Formalin-fixed, Paraffin-embedded Tissue
Study
EGAS00001004293
-
The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Study
EGAS00001002218
-
Rare occurrence of Aristolochic Acid Mutational Signatures in Oro-Gastrointestinal Tract Cancers
Study
EGAS00001005909
-
Hereditary Cancer Diagnostics with I2HCP gene panel
Study
EGAS00001004316
-
TSG_knock_out_in_hiPSCs
Study
EGAS00001002262
-
WGS_of_AML_during_PARPi_therapy
Study
EGAS00001002274
-
Single-cell RNA sequencing of 6 follicular lymphoma tumors
Study
EGAS00001005257
-
Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
Oesophageal_Adenocarcinoma_Organoid_10x
Study
EGAS00001003191
-
Comprehensive molecular characterization of brainstem glioma
Study
EGAS00001004341
-
DNA sequencing for human normal endometrial glands
Study
EGAS00001005822
-
Control samples, breast cancer clinical samples and matched patient-derived tumour xenografts (PDTXs) to develop and test a computational approach to discriminate human and mouse sequences in PDTXs
Study
EGAS00001002445
-
Target gene sequencing for human normal endometrial glands
Study
EGAS00001005914
-
Genomic determination for Homologous Recombination Deficiency (HRD) by shallow Whole Genome Sequencing (sWGS)
Study
EGAS00001005926
-
Genetic Risk for Subsequent Neoplasms among Long-term Survivors of Childhood Cancer in the St. Jude Lifetime Cohort
Study
EGAS00001002499