-
Long-term organoid culture of a small intestinal neuroendocrine tumor rna-seq
Study
EGAS00001007108
-
ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Cardiovascular disease biomarkers derived from circulating cell-free DNA methylation
Study
EGAS00001007263
-
Whole-Genome sequencing of hepatocellular carcinomas
Study
EGAS00001000706
-
Phylogenetic analysis of paired breast carcinomas identifies genetic events associated with clonal recurrence and invasive progression
Study
EGAS50000001298
-
Single_Cell_Sequencing_of_Sperm__scSperm_
Study
EGAS00001000935
-
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Study
EGAS00001001000
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal
Study
EGAS00001003774
-
Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring
Study
EGAS00001003963
-
Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
-
Pancreatic tropism of metastatic renal cell carcinoma
Study
EGAS00001004208
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183
-
CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA
Study
EGAS00001002211
-
Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas
Study
EGAS00001000572
-
Accurate sample assignment in a multiplexed, ultra-sensitive, high-throughput sequencing assay for minimal residual disease
Study
EGAS00001001303
-
Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Study
EGAS00001002440
-
High Grade Serous Ovarian Carcinomas Originate in the Fallopian Tube
Study
EGAS00001002589
-
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
-
Single cell transcriptomic landscape of pediatric B-cell acute lymphoblastic leukemia: dissection of transcriptional heterogeneity and B-cell developmental state
Study
EGAS00001007512
-
Ewing and Ewing-like-sarcoma tumoroid biobank reveals distinct drug sensitivities: translocation makes the difference
Study
EGAS00001007941
-
Pooled scRNA-seq of iPSC-derived neural stem cells from ADHD and control individuals
Study
EGAS00001008169
-
Genomic profiling of Acute Lymphoblastic Leukemia in Ataxia Telangiectasia patients reveals tight link between ATM mutations and chromothripsis
Study
EGAS00001002270
-
Recurrent intra-tumour heterogeneity is a hallmark of metastatic prostate cancer
Study
EGAS50000001312
-
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
-
Botswana 15 autosomal unlinked microsatellites
Study
EGAS00001002380
-
The evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion
Study
EGAS00001002432
-
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathy
Study
EGAS00001002454
-
Direct Detection of Early-stage Cancers Using Circulating Tumor DNA
Study
EGAS00001002577
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
CancerDetector: Ultrasensitive and Non-Invasive Cancer Detection at the Resolution of Individual Reads using Cell-free DNA Methylation Sequencing Data
Study
EGAS00001002728
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
Assessing gene expression profiling from FFPE Patient Samples: A Comparison of Two Library Preparation Approaches and Recommendations
Study
EGAS50000001066
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
UK10K_RARE_SIR
Study
EGAS00001000130
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-009
Study
EGAS00001004290
-
UK10K RARE CHD
Study
EGAS00001000125
-
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR02
Study
EGAS00001001028
-
Efficacy of two different FGFR-inhibitors in a patient with extrahepatic cholangiocarcinoma harboring an FGFR2 mutation
Study
EGAS50000000015
-
Cell type mapping of inflammatory muscle diseases highlights selective myofiber vulnerability in inclusion body myositis
Study
EGAS50000000310
-
P647_Targeted_resequencing_project
Study
EGAS00001000305
-
Identifying New Genetic Subtypes in Follicular Lymphoma
Study
EGAS50000000435
-
Exome sequencing of a novel cervical cancer cell line
Study
EGAS00001003343
-
IMPRESS: Improved methylation profiling using restriction enzymes and smMIP sequencing, combined with a new biomarker panel, creating a multi-cancer detection assay
Study
EGAS50000000624
-
Human inflammatory cardiomyopathies following SARS-CoV2 infection and COVID-19 vaccination
Study
EGAS50000000769
-
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Study
EGAS00001003438
-
Use of new methodologies to achieve a thorough molecular characterization in pediatric acute leukemia
Study
EGAS50000000701
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution
Study
EGAS00001003443
-
Molecular determinants of response to PD-L1 blockade across tumor types
Study
EGAS00001004343