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ERG ALTERATIONS DEFINE A NOVEL SUBTYPE OF ACUTE LYMPHOBLASTIC LEUKEMIA
Study
EGAS00001000514
-
An RCOR1 loss-associated gene expression signature identifies a prognostically significant DLBCL subgroup
Study
EGAS00001001000
-
Accurate sample assignment in a multiplexed, ultra-sensitive, high-throughput sequencing assay for minimal residual disease
Study
EGAS00001001303
-
Rare SNPs in receptor tyrosine kinases are negative outcome predictors in multiple myeloma
Study
EGAS00001001665
-
Recurrent somatic JAK-STAT mutations within a novel RUNX1-mutated pedigree
Study
EGAS00001001862
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
Genomics of enteropathy associated T cell lymphoma (EATL)
Study
EGAS00001001954
-
Whole genome sequencing of tumour and normal paired samples of diffuse intrinsic pontine gliomas
Study
EGAS00001000572
-
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia is Characterized by Distinct Genomic Subsets with Varying Outcomes
Study
EGAS00001002183
-
Whole-exome and targeted sequencing of pediatric hyperdiploid B-cell precursor acute lymphoblastic leukemia
Study
EGAS00001001113
-
Novel genes for Intellectual Disability identified using whole genome sequence and pathway analysis
Study
EGAS00001001386
-
Ethiopia_Genome_Project__high_coverage_
Study
EGAS00001000237
-
UK10K_RARE_NEUROMUSCULAR
Study
EGAS00001000101
-
UK10K_RARE_FIND
Study
EGAS00001000128
-
UK10K_RARE_CILIOPATHIES
Study
EGAS00001000126
-
UK10K_RARE_SIR
Study
EGAS00001000130
-
Stratifying and Targeting Pediatric Medulloblastoma through Genomics
Study
EGAS00001000273
-
UK10K RARE CHD
Study
EGAS00001000125
-
Genomic Alterations in Gingivo-buccal Cancer: ICGC-India Project_YR02
Study
EGAS00001001028
-
P647_Targeted_resequencing_project
Study
EGAS00001000305
-
The Genomic Landscape of Childhood and Adolescent Melanoma
Study
EGAS00001000901
-
Developmental_Dysplasia_of_the_Hip__DDH_
Study
EGAS00001000916
-
Comprehensive genomic profiles of small cell lung cancer
Study
EGAS00001000925
-
Exploring the role of mtDNA variation in Multiple Sclerosis in a large cohort of discordant monozygotic twins
Study
EGAS00001001240
-
Clonal selection and double hit events involving tumor suppressor genes underlie relapse from total therapy
Study
EGAS00001001810
-
A somatic reference standard for cancer genome sequencing with COLO829
Study
EGAS00001001385
-
The HLA-DQβ1 insertion is a strong achalasia risk factor and displays a geospatial north-south gradient among Europeans
Study
EGAS00001001515
-
Whole exome sequencing on primary retinoblastoma tissues and matching lymphocyte DNA.
Study
EGAS00001001690
-
Ethiopia_Genome_Project__low_coverage_
Study
EGAS00001000238
-
UK10K OBESITY TWINSUK
Study
EGAS00001000306
-
The Prediction and Prevention of Preeclampsia
Study
EGAS00001001898
-
Convergent somatic mutations in effectors of insulin signalling in chronic liver disease
Dataset
EGAD00001006255
-
PSCP_bisulphite analysis in hESCs (2018-08-13)
Dataset
EGAD00001004295
-
NIPT samples for systematic evaluation of NIPT aneuploidy detection software tools
Dataset
EGAD00001007712
-
Mutational landscape of normal epithelial cells in Lynch Syndrome patients
Dataset
EGAD00001008092
-
FASTQ files of total RNA-Seq data from the POPS PET (pre-eclamptic) samples
Dataset
EGAD00001003508
-
RNA-seq analysis of transcriptome variation with human ESC subclones
Dataset
EGAD00001004266
-
Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Dataset
EGAD00001007862
-
PSCP_bisulphite analysis in hESCs
Dataset
EGAD00001002235
-
FASTQ files of total RNA-Seq data from the POPS SGA (Small for Gestational Age) samples
Dataset
EGAD00001003507
-
Swarm Learning to identify COVID-19, tuberculosis and leukemia patients based on blood transcriptomes
Dataset
EGAD00001006231
-
PSCP_mutation analysis in hESCs
Dataset
EGAD00001002231
-
Whole Exome Sequencing PPGL
Study
EGAS00001006043
-
The Spatial Heterogeneity in Multiple Myeloma - from the Subclonal Architecture to the Immune Microenvironment (partly hipo_K08K)
Study
EGAS00001006090
-
Cardiovascular disease biomarkers derived from circulating cell-free DNA methylation
Study
EGAS00001007263
-
Human liver NPCs single cell project
Study
EGAS00001007194
-
Comparison of structural variations from 10X Genomics linked-reads and conventional Illumina short-reads sequencing
Study
EGAS00001004093
-
Pancreatic, Small-intestinal and Pulmonary Neuroendocrine Tumors
Study
EGAS00001004878
-
Sclerosing epithelioid fibrosarcoma case report
Study
EGAS00001005214
-
Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414