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Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in Metastasis
Study
EGAS00001001788
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The proliferative history shapes the DNA methylome of B-cell tumor and predicts clinical outcome
Study
EGAS00001004640
-
Risk and modifying factors in Frontotemporal Dementia
Study
EGAS00001004895
-
Single cell RNA sequencing of synovial B cells in early Rheumatoid Arthritis
Study
EGAS00001005144
-
Whole genome sequence and RNA-seq data from paired tumour and germline samples from mesothelioma patients.
Study
EGAS00001005196
-
Linking the epigenetic landscape in chronic lymphocytic leukemia to deregulated chromatin networks
Study
EGAS00001002518
-
Monitoring of leukemia clones in B-cell acute lymphoblastic leukemia at diagnosis and during treatment by single-cell DNA amplicon sequencing
Study
EGAS00001005029
-
TRACERx Renal 100
Study
EGAS00001002793
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228
-
Khoe-San genomes reveal unique variation and confirm deepest population divergence in Homo sapiens
Study
EGAS00001004459
-
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
-
De novo assembly of 150 Danish genomes reveals rich structural complexity
Study
EGAS00001002108
-
Resequencing (MIPS) of candidate genes for Keratoconus (2020)
Study
EGAS00001004267
-
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
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
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
-
An Atlas of Cells in the Human Tonsil
Study
EGAS00001006375
-
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
-
MutWP1: CRUK Grand Challenge Mutographs of Cancer: Oesophageal adenocarcinoma
Dataset
EGAD00001006083
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Functional single-cell characterization of immune aplastic anemia shows convergence of NK and NK-like CD8+ T cells with disease-associated TCR signature
Study
EGAS00001007602
-
Functional single-cell characterization of immune aplastic anemia shows convergence of NK and NK-like CD8+ T cells with disease-associated TCR signature
Study
EGAS00001007604
-
Discovery of immunotherapy targets for pediatric solid and brain tumors by exon-level expression
Study
EGAS00001007766
-
Genomic_Advances_in_Sepsis__GAinS__genotyping
Study
EGAS00001007786
-
H3Africa - Identification and characterization of novel hereditary neurological disease genes in Mali.
Study
EGAS00001003016
-
H3Africa - Kidney Disease Research Network
Study
EGAS00001006558
-
After the completion of CINECA, EUCANCan, and euCanSHare. What's next?
Blog
cineca-eucancan-and-eucanshare-were-concluded-in-june
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Surgical Treatment for Ischemic Heart Failure (STICH-BioLINCC)
Study
phs003493
-
EOSC4Cancer Longitudinal Synthetic Colorectal Cancer Genomic data developed at BSC
Dataset
EGAD50000000276
-
DIAMOND PCR : plasma DNA LINE-1 targeted bisulfite sequencing, a new non-invasive multi-cancer detection marker
Dataset
EGAD50000000646
-
Variant calling dataset from the whole-exome study of familial pulmonary fibrosis in the Canary Islands-VCF files
Dataset
EGAD50000001152
-
Low T cell diversity is associated with poor outcome in bladder cancer - Bulk TCRseq data
Study
EGAS50000000940
-
Microbiome
Dataset
EGAD50000002027
-
Catalogue Statistics
Documentation
about/statistics/catalogue
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RNA-seq FASTQ files from newborn screening dried blood spot samples
Dataset
EGAD00001004991
-
Profiling molecular heterogeneity in human primary microglia
Dataset
EGAD00001005736
-
WES data for Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Dataset
EGAD00001015413
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006643
-
The mutational landscape of human somatic and germline cells
Dataset
EGAD00001006642
-
PELICAN33 Phenomic Dataset
Dataset
EGAD00001007800
-
Prediction of HLA genotypes using NGS data
Dataset
EGAD00001007733
-
Transcriptome Analysis of Malignant Peripheral Nerve Sheath Tumor-like Melanoma
Dataset
EGAD00001007000
-
Somatic L1 retrotransposition in normal colorectal epthelium
Dataset
EGAD00001010183