-
HSC_population_dynamics_KSP_samples
Study
EGAS00001002762
-
Diet driven microbial ecology underpins associations between cancer immunotherapy outcomes and the gut microbiome
Study
EGAS00001006982
-
CINECA_synthetic_cohort_EUROPE_UK1 referencing fake samples
Dataset
EGAD00001006673
-
pancreatic ductal adenocarcinoma exomes in study: Pro-immunogenic Impact of MEK inhibition combined with an anti-CD40 immunostimulatory antibody
Study
EGAS00001004196
-
Evolution of an adenomacarcinoma in response to selection by targeted kinase inhibitors
Study
EGAS00000000074
-
Quantification of chromosomal copy number aberrations by shallow whole-genome sequencing
Study
EGAS00001000642
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis
Study
EGAS00001001258
-
Sequencing-based counting and size profiling of plasma Epstein-Barr virus DNA enhance population screening of nasopharyngeal carcinoma.
Study
EGAS00001002707
-
Oncogenic fate conversion by PRDM16s causes acute myeloid leukemia
Study
EGAS00001003235
-
Healthspan and lifespan extension by fecal microbiota transplantation in progeroid mice
Study
EGAS00001003656
-
Neoadjuvant immunotherapy leads to pathological responses in MMR proficient and MMR deficient early stage colon cancers
Study
EGAS00001004160
-
Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib
Study
EGAS00001004539
-
Robust methylation-based classification of brain tumours using nanopore sequencing
Study
EGAS00001006540
-
Non-viral precision T cell receptor replacement for personalized cell therapy
Study
EGAS00001006898
-
Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
eMERGE: Genetics of Complex Pediatric Disorders from the Center for Applied Genomics
Study
phs001165
-
STAMPEED: Whole Genome Association Analysis of Hematopoietic Cell Transplant (HCT) Outcomes
Study
phs001918
-
Prader-Willi Syndrome and Early-onset Morbid Obesity Natural History Protocol
Study
phs000575
-
Kids First: Genomic Etiologies of CHARGE Syndrome, Related Conditions and Structural Anomalies
Study
phs002592
-
sWGS of HGSOC samples for fixative comparison study
Dataset
EGAD00001001938
-
The mutational landscape of skin tumours in CYLD cutaneous syndrome determined
Dataset
EGAD00001004573
-
Targeted Myeloid DNA-Panelsequencing, MLL
Dataset
EGAD00001008485
-
Guardians_of_the_genome__protecting_DNA_from_endogenous_sources_of_damage_
Study
EGAS00001000874