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Exome sequencing
Study
EGAS00001005761
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Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
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Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements
Study
EGAS00001003415
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Neuroblastoma tumor heterogeneity and cell plasticity (from PDX and cell lines)
Study
EGAS00001004781
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Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
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Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
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Capturing sex-specific and infertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome
Study
EGAS00001006643
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STREP GENE: Genetics and Severe Streptococcal Infections
Study
EGAS00001003421
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Molecular landscape of blastic plasmacytoid dendritic cell neoplasm
Study
EGAS00001006166
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Study the genetic susceptibility of esophagus squamous cell carcinomas (ESCC) in high-risk area Henan Chinese
Study
EGAS00001003423
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Genomic_profiling_of_B_other_Adult_ALL_RNA
Study
EGAS00001003428
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Genomic analysis of a hypermutated gliosarcoma
Study
EGAS00001004864
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Targeted de-methylation of the FOXP3-TSDR
Study
EGAS00001004867
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Proteogenomics of chronic lymphocytic leukemia
Study
EGAS00001005746
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Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas
Study
EGAS00001003430
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Functional and genomic heterogeneity of long-term self-renewing compartment as the origin of treatment resistance in pancreatic tumors
Study
EGAS00001003442
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Analysis of error profiles in deep next-generation sequencing data
Study
EGAS00001003444
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BinDel: software tool for detecting clinically significant microdeletions in low-coverage WGS-based NIPT samples
Study
EGAS00001006663
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Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Study
EGAS00001005863
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Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing
Study
EGAS00001005872
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Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors
Study
EGAS00001006205
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Adenoma to Carcinoma transition in Colorectal Cancer
Study
EGAS00001003468
-
Dedifferentiated_Melanoma
Study
EGAS00001003471
-
Exome sequencing of synchronous colorectal cancers
Study
EGAS00001003474
-
The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
-
The Proteogenomic Subtypes of Acute Myeloid Leukemia
Study
EGAS00001005950
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MutWP5__CRUK_Mutographs_of_Cancer__BRCA_Carriers___WG__Novaseq_
Study
EGAS00001003523
-
An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs
Study
EGAS00001005974
-
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma (H033)
Study
EGAS00001003481
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Comprehensive epigenomic profiling reveals the extent of disease-specific chromatin states and informs drug target discovery in ankylosing spondylitis
Study
EGAS00001006233
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Human genome-wide variations in the Massim region
Study
EGAS00001006010
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq)
Study
EGAS00001006017
-
EXCEED Study
Study
EGAS00001003499
-
Chromatin profiles classify castration-resistant prostate cancers suggesting therapeutic targets
Study
EGAS00001006059
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GENOMIC MUTATION LANDSCAPE OF SKIN CANCERS FROM DNA REPAIR-DEFICIENT XERODERMA PIGMENTOSUM PATIENTS
Study
EGAS00001006732
-
Data containing genome-wide SNP data from Northwestern Amazonia
Study
EGAS00001006767
-
Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer
Study
EGAS00001006118
-
Genetic immune escape landscape in primary and metastatic cancer
Study
EGAS00001006123
-
Genetic regulation of gene expression in human brain cell types
Study
EGAS00001006345
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Pancreatic_Organoids
Study
EGAS00001003520
-
Loss of Epigenetic Barrier is Required for Enhancer Hijacking-Mediated Oncogenic Transcription
Study
EGAS00001006140
-
Single cell multi-omic data of glioblastoma evolution under therapy
Study
EGAS00001004909
-
Mapping genetic effects on cell type-specific chromatin accessibility using single nucleus ATAC-seq
Study
EGAS00001006184
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MutWP5__CRUK_Mutographs_of_Cancer__Cancer_Mastectomy__Exome__Novaseq_
Study
EGAS00001003528
-
Long-term temporal stability of peripheral blood DNA methylation alterations in patients with inflammatory bowel disease.
Study
EGAS00001006501
-
MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__clear_cell_renal_cell_carcinoma___2
Study
EGAS00001003542
-
DNA methylation atlas of normal human cell types
Study
EGAS00001006791
-
Rare coding variants in lupus risk genes
Study
EGAS00001003548
-
Genetic and epigenetic variation at regulatory regions contribute to cancer evolution under endocrine treatment
Study
EGAS00001006340
-
Insights from genome-wide data from Thailand and Laos
Study
EGAS00001006053