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SS18-SSX-mediated hijacking of BAF complexes drives synovial sarcoma
Study
EGAS00001002920
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
Kidney_transplant_nephrectomy_scRNAseq
Study
EGAS00001003935
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
Patient-derived neuroblastoma model system OHC-NB1
Study
EGAS00001003031
-
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
BARIA baseline first 100 individuals transcriptomes
Study
EGAS00001005704
-
A Single-cell Atlas of Progressive TKI Resistance in Chronic Myeloid Leukemia
Study
EGAS00001005509
-
Molecular_risk_stratification_in_patients_with_T1_colorectal_cancer_WES
Study
EGAS00001005734
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001005784
-
De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
B cell receptor repertoire kinetics after SARS-CoV-2 infection and vaccination
Study
EGAS00001005816
-
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing
Study
EGAS00001003190
-
Target gene sequencing for human normal endometrial glands
Study
EGAS00001005914
-
Full blood mRNA sequencing of myotonic dystrophy type 1 patients after cognitive behavioural therapy
Study
EGAS00001005830
-
Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
-
Targeted sequencing of diffuse large B-cell lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005953
-
Changes in alternative splicing and associated neo-antigens due to therapy
Study
EGAS00001004524
-
Patient-tailored design for selective co-inhibition of leukemic cell subpopulations
Study
EGAS00001004614
-
Allele-specific expression of GATA2 due to epigenetic dysregulation in double mutated CEBPA AML
Study
EGAS00001004684
-
Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
Heat selection enables highly scalable methylome profiling in cell-free DNA for noninvasive monitoring of cancer patients
Study
EGAS00001006198
-
Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
Study
EGAS00001006200
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
MGP Panel: a comprehensive targeted genomics panel for molecular profiling of multiple myeloma patients
Study
EGAS00001006222
-
Discovery of a highly widespread bacteriophage family and its associations to metabolic syndrome gut microbiomes
Study
EGAS00001006260
-
Clonal relationships of ductal carcinoma in situ and recurrent invasive breast cancers defined by genomic analysis
Study
EGAS00001006306
-
Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers
Study
EGAS00001003556
-
An Atlas of Cells in the Human Tonsil
Study
EGAS00001006375
-
PDAC organoid genomic heterogeneity
Study
EGAS00001006782
-
Genomic_characterisation_of_MGUS__
Study
EGAS00001004124
-
Treatment-mediated selection of lethal prostate cancer clones defined by copy number architectures
Study
EGAS00001006598
-
DNA methylation landscape of prostate cancer
Study
EGAS00001006670
-
Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma
Study
EGAS00001006692
-
Targeted therapy of advanced parathyroid carcinoma guided by genomic and transcriptomic profiling (hipo_021)
Study
EGAS00001006747
-
The impact of BNT162b2 mRNA vaccine against SARS-CoV-2 on adaptive and innate immune responses
Study
EGAS00001006818
-
Case Report: Rare IKZF1 gene fusions identified in neonate with congenital KMT2A-rearranged Acute Lymphoblastic Leukemia
Study
EGAS00001006947
-
Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children
Study
EGAS00001005461
-
The immunological characterization of expanded tumor-infiltrating lymphocytes in renal cell carcinoma patients
Study
EGAS00001006952
-
Gut microbiome dynamics unravelled with metagenomics sequencing
Blog
gut-microbiome-dynamics-unravelled
-
Genome Diversity in Africa Project: Benin (2021-02-16)
Dataset
EGAD00001006970
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Oesophageal adenocarcinoma
Dataset
EGAD00001006083
-
CM067 WES - Clinical Outcomes by Tumor Mutational Burden and Inflammatory Gene Expression With Combined Nivolumab and Ipilimumab or Monotherapy in Advanced Melanoma
Dataset
EGAD00001007573
-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001009048
-
Whole genome sequencing of retinoblastoma reveals the diversity of rearrangements disrupting RB1 and uncovers a treatment related mutational signature
Dataset
EGAD00001006431
-
panALL exome data set3, 650 samples
Dataset
EGAD00001008290
-
RNA-seq of high grade serous ovarian tumours
Dataset
EGAD00001010139
-
Medulloblastoma cfDNA low-coverage WGS
Dataset
EGAD00001008277