-
Correction of the cytosine deamination artifacts in FFPE-based sequencing experiments
Study
EGAS50000001354
-
ABHD11 inhibition drives sterol metabolism to modulate T cell effector function and alleviate autoimmunity
Study
EGAS50000001297
-
NOUS-209 off-the-shelf immunotherapy has the potential to hit primary and metachronous colorectal and urothelial cancer in Lynch syndrome
Study
EGAS50000001336
-
Single-nuclei histone modification profiling of the adult human central nervous system unveils epigenetic memory of developmental programs
Dataset
EGAD50000000410
-
A non-canonical lymphoblast in refractory childhood T-cell leukaemia
Study
EGAS50000000767
-
Aberrant expression of SLAMF6 constitutes a targetable immune escape mechanism in acute myeloid leukemia
Study
EGAS50000001085
-
WES analysis of paired tumor and non-tumoral DNA of 4 patients with non-muscle-invasive bladder cancer
Study
EGAS50000001382
-
Oligodendroglia as functional effectors of Multiple Sclerosis risk variants (iPS derived hOPC scCRISPRi/a-seq)
Study
EGAS50000001417
-
Adult B-precursor acute lymphoblastic leukemia RoCK and ROI single-cell transcriptome
Study
EGAS50000001366
-
Whole genome sequencing data of paediatric KMT2A-rearranged acute lymphoblastic leukemia
Study
EGAS50000001079
-
B cell activation
Study
EGAS50000001468
-
Comprehensive genetic landscape, immune checkpoint profiling, and establishment of patient-derived xenograft (PDX) of metachronous brain tumors from constitutive mismatch repair deficiency with a biallelic variant on MSH6
Study
EGAS50000000351
-
Drug Perturbation of Primary Lymphoma Patient Samples and RNA Sequencing
Study
EGAS50000001500
-
Paired DNA and RNA sequencing uncovers common and rare genomic variants regulating gene expression in the human retina
Study
EGAS50000001443
-
RNAseq profile of monomorphic epitheliotropic intestinal T-cell lymphoma and enteropathy associated T-cell lymphoma
Study
EGAS50000001125
-
Whole Exome Sequencing of monomorphic epitheliotropic intestinal T-cell lymphoma and enteropathy associated T-cell lymphoma
Study
EGAS50000001126
-
Transcriptomic profiles studies CAREs group - IDIBGI
Dac
EGAC50000000607
-
Transcriptomic profiling of skin biopsies from psoriasis patients following treatment with Zasocitinib
Study
EGAS50000001548
-
RNAseq of MCL cell lines
Study
EGAS50000001087
-
PD-associated regulatory variants in human dopaminergic neurons reveals modulators of SCARB2 and BAG3 expression
Dataset
EGAD50000002258
-
Discordant_Monozygotic_Twins_ALS(Transcriptomics)
Study
EGAS50000000909
-
Transcriptional characterization of human innate lymphoid cells (ILCs) and natural killer (NK) cells from fresh umbilical cord blood
Study
EGAS50000001204
-
Bleomycin Induced Pneumonitis cohort of the Exceptional Responders Program of the Garvan Institute of Medical Research
Study
EGAS50000001545
-
Spatial predictors of response to immunotherapy in microsatellite stable metastatic colorectal cancer
Dataset
EGAD50000002244
-
Identification_of_drug_resistance_genes_in_cancer_cell_lines_by_insertional_mutagenesis
Study
EGAS00001001035
-
463 newly diagnosed patients with Multiple Myeloma underwent whole exome sequencing of tumour and peripheral blood DNA.
Study
EGAS00001001147
-
Breast Cancer - Very young women
Study
EGAS00001001908
-
Genetic_background_for_cardio_vascular_disorders_in_the_general_Finnish_population
Study
EGAS00001000229
-
RNA_sequencing
Study
EGAS00001000310
-
Longitudinal analysis of treatment induced genomic alterations in gliomas
Study
EGAS00001002168
-
Canadian Prostate Cancer Genome Network
Study
EGAS00001000900
-
ICGC Oesophageal adenocarcinoma - lymph-node samples
Study
EGAS00001000727
-
Leucocyte eQTLs in autoimmune disease and health
Study
EGAS00001001251
-
Novel Epigenetic Markers for Toxicity after Intraoperative and Conventional Radiotherapy for Breast Cancer
Study
EGAS00001001279
-
HipSci___RNAseq___Rare_BBS
Study
EGAS00001001318
-
RNA-seq analysis of megakaryocytes and granulocytes in Quebec platelet disorder
Study
EGAS00001001840
-
TMD_AMKL_targeted_follow_up
Study
EGAS00001000569
-
The_Causes_of_Clonal_Blood_Cell_Disorders_Study___SCOR
Study
EGAS00001002132
-
Methylation_changes_in_OA_patients_with_chronic_exposure_to_cobalt_and_chromium
Study
EGAS00001001180
-
Lethal malformation syndrome
Study
EGAS00001000061
-
Hypermutation of the inactive X chromosome is a frequent event in cancer
Study
EGAS00001000565
-
Illumina ExomeChip genotyping data from the Cretan Greek isolate collection HELIC MANOLIS
Study
EGAS00001000630
-
TMD_AMKL_targeted_follow_up_part_2
Study
EGAS00001000732
-
A WTCCC2 genome-wide association study for psychosis endophenotype (PE) in individuals from UK, Germany, Holland, Spain and Australia.
Study
EGAS00001000817
-
Transcriptomics_of_human_olfactory_mucosa
Study
EGAS00001001486
-
Linking genes, genomic instability and molecular subgroups in medulloblastoma
Study
EGAS00001000085
-
PAS Pedigrees: Identification of novel genetic variants contributing to cardiovascular disease in pedigrees with premature atherosclerosis.
Study
EGAS00001000052
-
Whole genome bisufite sequencing of smoking and non-smoking mother-child pairsBisufite sequencing, RNA-seq and ChIP-Seq data of whole blood samples from smoking and non-smoking mothers and their children at gestation/birth and follow-up years.
Study
EGAS00001000455
-
Genetic landscape of pediatric Infant Acute Lymphoblastic leukemia
Study
EGAS00001000246
-
DNA from colon cancer samples and matched normal samples was hybridized on Human 660W-Quad SNP arrays and sequenced in Illumina HiScanSQ.
Study
EGAS00001000558