-
CD49f single-cell methylomes
Study
EGAS00001002789
-
Population_dynamics_in_abnormal_haematopoiesis
Study
EGAS00001003181
-
The double-hit signature identifies double-hit diffuse large B-cell lymphoma with genetic events cryptic to FISH
Study
EGAS00001004285
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
RNA-sequencing data from 195 B-cell precursor acute lymphoblastic leukemias and mate pair whole genome sequencing data from 15 B-cell precursor acute lymphoblastic leukemias
Study
EGAS00001001795
-
PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice
Study
EGAS00001002903
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
502 present-day genotypes included in the '137 ancient human genomes from across the Eurasian steppe' publication
Study
EGAS00001002926
-
503 genotypes from Inner Asia used in 'Close inbreeding and low genetic diversity in Inner Asian human populations despite geographical exogamy' publication
Study
EGAS00001002951
-
A genome scan for genes underlying adult body size differences between Central African hunter-gatherers and farmers.
Study
EGAS00001002975
-
CTCF/cohesin-binding sites are frequently mutated in cancer
Study
EGAS00001003010
-
Allele Balance Bias Identifies Systematic Genotyping Errors and False Disease Associations
Study
EGAS00001003027
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
FBSeq: RNA sequencing of human fetal brain.
Study
EGAS00001003214
-
Genome_Diversity_in_Africa_Project___GemCode_libraries
Study
EGAS00001001589
-
WES analysis in identifying additive genetic factors that may contribute to the occurrence of moyamoya in neurofibromatosis type 1
Study
EGAS00001003053
-
Indonesian Genome Diversity Project
Study
EGAS00001003054
-
The evolutionary landscape of colorectal tumorigenesis
Study
EGAS00001003066
-
SLC9A3R1 variant associated with age-related hearing loss
Study
EGAS00001003072
-
Ovarian cancer organoid biobank
Study
EGAS00001003073
-
UK10K COHORT ALSPAC
Study
EGAS00001000090
-
Exome sequencing of advanced hepatocellular carcinoma
Study
EGAS00001003130
-
Exome_Sequencing__to_Identify_Causes_of_Leukaemia_Predisposing_Congenital_Neutropenias
Study
EGAS00001000100
-
High Altitude Pulmonary Hypertension
Study
EGAS00001003171
-
UK10K_RARE_HYPERCHOL
Study
EGAS00001000129
-
A Single Complex Agpat2 Allele In A Patient With Partial Lipodystrophy
Study
EGAS00001003177
-
HipSci_Illumina 450K Methylation analysis_Healthy volunteers
Study
EGAS00001000865
-
Genetic_factors_underlying_premature_coronary_heart_disease_in_patients_with_normal_coronary_arteries
Study
EGAS00001000133
-
Low frequency and rare coding variation contributes to multiple sclerosis risk
Study
EGAS00001003195
-
Matched_Pair_Cancer_Cell_line_Whole_Genomes
Study
EGAS00001000160
-
Genome-wide association study of cervical cancer in East Asian populations
Study
EGAS00001003199
-
Assessment_of_genetic_and_epigenetic_variation_in_human_IPS_cells_RNA
Study
EGAS00001000367
-
Epigenetics/genetics of the patient-derived xenografts of pediatric T-cell leukemia
Study
EGAS00001003248
-
Comparison of EGF and PDGF driven glioblastomas.
Study
EGAS00001001900
-
1 Intratumoral genetic heterogeneity and clonal evolution following neoadjuvant chemoradiotherapy (nCRT) in locally advanced rectal tumors.
Study
EGAS00001003250
-
MYCN Amplification and ATRX Mutations are Incompatible in Neuroblastoma
Study
EGAS00001003257
-
Preeclampsia InterPregGen Consortium: Whole Genome Sequencing of 100 unrelated Kazakhs (DNA samples from the Scientific Center of Obstetrics, Gynecology and Perinatology, Almaty, Kazakhstan; Gulnara Svyatova, Principal Investigator
Study
EGAS00001000417
-
Genomic landscape of oral cancers (Complete Genomics WGS)
Study
EGAS00001002393
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - RNA-seq
Study
EGAS00001003274
-
Genetic characterization of B-cell prolymphocytic leukemia: a hierarchical prognostic model involving MYC and TP53 abnormalities - WXS
Study
EGAS00001003275
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__Exome_
Study
EGAS00001003313
-
MutWP5__CRUK_Mutographs_of_Cancer__Breast__Reduction_Mammoplasty__WG_
Study
EGAS00001003311
-
STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
-
MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___Exome__Novaseq_
Study
EGAS00001003526
-
Whole genome sequencing with linked reads of pediatric glioblastoma samples
Study
EGAS00001003432
-
Intratumoural Heterogeneity Underlies Distinct Therapy Responses and Treatment Resistance in Glioblastoma
Study
EGAS00001003438
-
Sequencing_probands_and_families_with_severe_insulin_resistance_syndromes
Study
EGAS00001000488
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Colorectal_LCM
Study
EGAS00001003455
-
An efficient and comprehensive strategy for genetic diagnostics of polycystic kidney disease
Study
EGAS00001001003