-
Mutational signatures in normal tissues of patients treated with clinical stage G-quadruplex binder CX5461
Study
EGAS50000001145
-
Transcriptome profiling of megakaryocytes and platelets: application to GP9- and IKZF5-related thrombocytopenia
Study
EGAS50000001276
-
Complex genotype-phenotype relationships shape the response to treatment of Down Syndrome Childhood Acute Lymphoblastic Leukaemia
Study
EGAS50000001287
-
Heterogeneity of IKZF1 genomic alterations and risk of relapse in childhood B-cell precursor acute lymphoblastic leukemia
Study
EGAS50000000106
-
WES analysis of a mixed cohort of pituitary tumors
Study
EGAS00001001714
-
Genome-Wide Association Study of aspirin-induced PUD in a UK cohort
Study
EGAS00001002052
-
Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Study
EGAS00001000652
-
Exome sequencing of uterine leiomyosarcomas
Study
EGAS00001001612
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
DNA methylation and the adverse metabolic outcomes of adiposity
Study
EGAS00001001922
-
Methylation differences in trisomy 21 using monozygotic twins
Study
EGAS00001001051
-
RB Loss in Resistant EGFR Mutant Lung Adenocarcinomas that Transform to Small Cell Lung Cancer
Study
EGAS00001001102
-
High-throughput Detection of Clinically Relevant Mutations in Archived Tumor Samples By Multiplexed PCR and Next Generation Sequencing
Study
EGAS00001000674
-
Exome Sequencing Of 75 Individuals From Multiply Affected Coeliac Families
Study
EGAS00001001093
-
UK10K NEURO FSZNK
Study
EGAS00001000119
-
UK10K NEURO ASD SKUSE
Study
EGAS00001000114
-
UK10K_NEURO_MUIR
Study
EGAS00001000122
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Chromatin immunoprecipitation linked to next-generation whole genome sequencing (ChIP-Seq) for H3K36me3 in paediatric high grade glioma cell lines KKNS4 and SF188 with and without a G34V mutation in H3F3A
Study
EGAS00001001437
-
Spatial and temporal evolution of distal 10q deletion, a prognostically unfavorable event in diffuse low-grade gliomas
Study
EGAS00001000643
-
Study on the consequences of prenatal famine exposure on DNA methylation.
Study
EGAS00001000668
-
Dilgom_Exome
Study
EGAS00001000086
-
Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Study
EGAS00001000642
-
Prediction and quantification of splice events from RNA-seq data
Study
EGAS00001001026