-
Dissection of the molecular complexity of colorectal cancer in pre-clinical models identifies predictive signatures of sensitivity to EGFR inhibitors
Study
EGAS00001001752
-
Gain of function DNMT3A mutations cause microcephalic dwarfism and hypermethylation of Polycomb-regulated regions
Study
EGAS00001003231
-
Sequencing of pancreatic cancer primary tumors and metastases
Study
EGAS00001002186
-
Aplastic anemia
Study
EGAS00001001153
-
AML_WES
Study
EGAS00001001559
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis
Study
EGAS00001001386
-
Establishing multiple omics baselines for three Southeast Asian populations in the Singapore Integrative Omics Study
Study
EGAS00001002527
-
Genomic analysis reveals novel secondary drivers and progression pathways in skin basal cell carcinoma
Study
EGAS00001001540
-
ALPI deficiency causes refractory Inflammation Bowel Disease
Study
EGAS00001003350
-
The spatial organization of intratumor heterogeneity andevolutionary trajectories of metastases in hepatocellular carcinoma
Study
EGAS00001001603
-
UK10K NEURO IOP COLLIER
Study
EGAS00001000121
-
Genetic landscape of Early T-cell precursor acute lymphoblastic leukaemia
Study
EGAS00001000348
-
Small molecule inhibitors of LOXL synergize with 5-AZA to restore erythropoiesis in myeloid neoplasms
Study
EGAS00001006174
-
Genome-wide mutation analysis of germinal-center B-cell derived lymphomas within the ICGC MMML-Seq Consortium
Study
EGAS00001000394
-
Cancer_Cell_Line_Exome_Sequencing_
Study
EGAS00001000978
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
TBA
Study
EGAS00001000803
-
Uveal melanoma patient with germline MBD4 nonsense mutation
Study
EGAS00001003362
-
Germline variants in the SEMA4A gene predispose to familial colorectal cancer type X
Study
EGAS00001000957
-
Spatio-temporal evolution of the primary glioblastoma genome
Study
EGAS00001001041
-
Efficacy of nivolumab in pediatric cancers with high mutation burden and mismatch-repair deficiency
Study
EGAS00001007393
-
Single-cell RNA sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004233
-
Human_Colorectal_Cancer_Exome_Sequencing
Study
EGAS00001000077
-
CRLF2_sequencing_project_
Study
EGAS00001000080
-
Linking genes, genomic instability and molecular subgroups in medulloblastoma
Study
EGAS00001000085
-
Targeted_NanoSeq_Buccal
Study
EGAS00001005925
-
UK10K COHORT TWINSUK
Study
EGAS00001000108
-
Family-based GWAS for CRSwNP
Study
EGAS00001002665
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
Therapeutic Targeting of Ependymoma as Informed by Oncogenic Enhancer Profiling
Study
EGAS00001002696
-
UK10K NEURO ASD TAMPERE
Study
EGAS00001000115
-
UK10K NEURO EDINBURGH
Study
EGAS00001000117
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty___WG__Novaseq_
Study
EGAS00001003524
-
Understanding_the_multicellular_dynamics_of_clear_cell_renal_cell_carcinoma___DNA_sequencing
Study
EGAS00001003517
-
UK10K NEURO FSZ
Study
EGAS00001000118
-
The integrated genomic and immune landscapes of lethal metastatic breast cancer.
Study
EGAS00001002703
-
Identification_of_drug_resistance_genes_in_melanoma_by_mRNA_gene_expression
Study
EGAS00001000815
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
Evolution of GBM through therapy
Study
EGAS00001003546
-
2014_AML_WES_51 samples
Study
EGAS00001002819
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T-cell lymphomas with hemophagocytic lymphohistiocytic syndrome
Study
EGAS00001002765
-
Single cell transcriptomic and genomic profiling of carcinogenesis in patients with familial adenomatous polyposis
Study
EGAS00001003598
-
UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
UK10K NEURO IMGSAC
Study
EGAS00001000120
-
Neoantigen responses to Immunotherapy in Prostate Cancer
Study
EGAS00001004050
-
UK10K RARE COLOBOMA
Study
EGAS00001000127
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000198
-
Cancer_Exome_Resequencing
Study
EGAS00001000206
-
Genetic characterization patients affected by Cancer of Unknown Primary
Study
EGAS00001006621
-
MMR (DNA mismatch repair) pathway in human samples
Study
EGAS00001002694
-
ICGC PedBrain: Deep-sequencing of childhood brain tumors.
Study
EGAS00001000215
-
Genomic profiling of matched well differentiated and de-differentiated liposarcoma.
Study
EGAS00001002807
-
Stratifying and Targeting Pediatric Medulloblastoma through Genomics
Study
EGAS00001000273
-
De_novo_mutations_in_cell_free_foetal_DNA__cffDNA_
Study
EGAS00001000322
-
Breast_Cancer_Somatic_Genetics_Study_
Study
EGAS00001000195
-
Myeloproliferative_Disorder_Sequencing
Study
EGAS00001000199
-
Targeted_NanoSeq___TwinsUK_Blood
Study
EGAS00001007595
-
The spatio-temporal evolution of lymph node spread in early breast cancer
Study
EGAS00001002947
-
UK10K RARE CHD
Study
EGAS00001000125
-
Parallel Detections of Somatic Gene Mutations in Surgically Resected Tumor tissues and Matched Plasma Specimens in Early-Stages of Primary Breast Cancer
Study
EGAS00001003075
-
RNA-seq, WGS and WES of Hepatocellular carcinomas, enriched in fibrolamellar carcinomas
Study
EGAS00001003837
-
UK10K NEURO GURLING
Study
EGAS00001000225
-
Integrative_Oncogenomics_of_multiple_myeloma
Study
EGAS00001000244
-
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR01
Study
EGAS00001000249
-
SSBP1
Study
EGAS00001004003
-
WGS/RNA-seq pair of an inflammatory hepatocellular adenoma (IHCA)
Study
EGAS00001003025
-
A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma
Study
EGAS00001003974
-
Wilm's tumor sequencing data
Study
EGAS00001005690
-
Genomic and transcriptomic profiling of combined hepatocellular and intrahepatic cholangiocarcinoma reveals distinct molecular subtypes
Study
EGAS00001003093
-
Targeted_EMSeq___Development
Study
EGAS00001007202
-
Renal_Follow_Up_Series
Study
EGAS00001000095
-
Location specific ACVR1, FGFR1 and TP53 mutations in pediatric glioblastomas in conjunction with H3.3 K27M.
Study
EGAS00001000720
-
Molecular Characterization of ETMRs
Study
EGAS00001003256
-
Clonal evolution study of Intrahepatic cholangiocarcinoma in Zhongshan Hospital
Study
EGAS00001002625
-
Pancreatic tropism of metastatic renal cell carcinoma
Study
EGAS00001004208
-
Targeted_NanoSeq_Sperm
Study
EGAS00001005920
-
Whole transcriptome sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004232
-
BLUEPRINT RNA-seq data for common cells in the haematopoietic lineages, from adult and cord blood samples.
Study
EGAS00001000327
-
Crohn_s_Exome_Sequencing
Study
EGAS00001000385
-
Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors
Study
EGAS00001000708
-
Long-read trio sequencing of unsolved patients with intellectual disability
Study
EGAS00001004319
-
Integrative_Oncogenomics_of_multiple_myeloma
Study
EGAS00001000243
-
BLUEPRINT Bisulfite-seq (CNAG)
Study
EGAS00001000418
-
Prediction of HLA genotypes using NGS data
Study
EGAS00001005274
-
EORTC RP1335 SPECTA Lung cancer data
Study
EGAS00001004485
-
early onset lone atrial fibrillation case-control study
Study
EGAS00001003208
-
WES sequencing of malignant peripheral nerve sheath tumours
Study
EGAS00001004527
-
A Multifactorial Tumor and Immune Cell Profile Determines Response to Immune Checkpoint blockade in Melanoma
Study
EGAS00001004548
-
A GWAS for cutaneous leishmaniasis in Brazil
Study
EGAS00001004596
-
Mutational context and diverse clonal development in early and late bladder cancer
Study
EGAS00001000641
-
Exploiting evolutionary steering in cancer therapy
Study
EGAS00001003200
-
Clonal Driver Neoantigen Loss under EGFR TKI and Immune Selection Pressures
Study
EGAS00001007926
-
Korean Lung Cancer - 36 pair WES data
Study
EGAS00001002843
-
Multiomic profiling of early-passage melanoma cell lines.
Study
EGAS00001004536
-
Anaplastic_Meningioma_WGS_X10
Study
EGAS00001000859
-
Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
-
RE_NanoSeq___TwinsUK_Buccal
Study
EGAS00001007740
-
Network-based systems pharmacology identifies heterogeneity in LCK and BCL2 signaling and differential vulnerability of T-cell acute lymphoblastic leukemia to targeted therapy
Study
EGAS00001004700