-
T cell receptor repertoire sequencing reveals chemotherapy-driven clonal expansion in colorectal liver metastases
Study
EGAS00001007136
-
Bacterial SNPs in the human gut microbiome associate with host BMI
Study
EGAS00001007204
-
Evolutionary origin and methylation status of human intronic CpG islands that are not present in mouse
Study
EGAS00001000719
-
Cistrome-partitioning reveals convergence of somatic mutations and risk-variants on master transcription regulators in primary prostate tumors
Study
EGAS00001003928
-
Characterization of HCV-specific CD4 T cells during DAA-Therapy
Study
EGAS00001003950
-
Molecular Attributes Underlying Central Nervous System and Systemic Relapse in Diffuse Large B-cell Lymphoma
Study
EGAS00001004057
-
UK10K_RARE_HYPERCHOL
Study
EGAS00001000129
-
Integration of genomics and histology reveals diagnosis and effective therapy of refractory cancer of unknown primary with PDL1 amplification (H021)
Study
EGAS00001001846
-
Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
-
Negligible impact on missing heritability of autoimmune-locus rare coding-region variants
Study
EGAS00001000476
-
Massively parallel nanowell-based single-cell gene expression profiling
Study
EGAS00001002320
-
Genome of the Netherlands
Study
EGAS00001000644
-
Cisplatin increases sensitivity to FGFR inhibition in patient-derived xenograft models of lung squamous cell carcinoma
Study
EGAS00001002423
-
Identification_of_synthetic_lethal_genes_by_CRISPR_Cas9_library
Study
EGAS00001002117
-
The evolutionary history of human colitis-associated colorectal cancer
Study
EGAS00001003028
-
Tissue-specific mutation accumulation in human adult stem cells during life
Study
EGAS00001001682
-
Germline variants collaborate with somatic mutations and initiate and/or drive disease in primary myelodysplastic syndrome (MDS) and therapy-related myeloid neoplasms (t-MN)
Study
EGAS00001003547
-
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Study
EGAS00001007573
-
Preclinical Pediatric Molecular Analysis for Therapy Choice (MATCH)
Study
EGAS00001008011
-
Genetic and epigenetic characterization of adenoid cystic carcinoma
Study
EGAS00001001457
-
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family
Study
EGAS00001002272
-
Successful BRAF/MEK-inhibition in a young patient with BRAF V600E-mutated extrapancreatic acinar cell carcinoma (HIPO-021)
Study
EGAS00001004282
-
UK10K COHORT TWINSUK
Study
EGAS00001000108
-
UK10K NEURO ASD BIONED
Study
EGAS00001000111
-
UK10K NEURO ASD GALLAGHER
Study
EGAS00001000112