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Long-read trio sequencing of unsolved patients with intellectual disability
Study
EGAS00001004319
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Persistent STAG2 mutation in recurrent pediatric glioblastoma
Study
EGAS00001004340
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The Medical Genome Reference Bank: a whole genome data resource of 4,000 healthy elderly individuals.
Study
EGAS00001003511
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Initial whole genome sequencing of plasma cell neoplasms in First Responders exposed to the World Trade Center attack of September 11, 2001
Study
EGAS00001004467
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Targets of MEK inhibition in DIPG
Study
EGAS00001004495
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RRBS sequencing of 7 tumour regions and a normal sample from a single TRACERx patient.
Study
EGAS00001002484
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Renal_habitat_WXS
Study
EGAS00001003703
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Copy number profiling of putative cancer stem from pleural effusion aspirates from breast cancer patients
Study
EGAS00001002343
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ATRX mutant neuroblastoma is sensitive to EZH2 inhibition via modulation of neuronal differentiation.
Study
EGAS00001002507
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Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia
Study
EGAS00001003975
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The Southern African Human Genome Programme
Study
EGAS00001002639
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Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
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DNA hypermethylation and differential gene expression associated with Klinefelter syndrome
Study
EGAS00001002797
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Atypical 3q26/MECOM rearrangements genocopy inv(3)/t(3;3) in acute myeloid leukemia
Study
EGAS00001004325
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WGS and WES data of invasive micropapillary carcinoma of breast
Dataset
EGAD00001008450
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Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing
Study
EGAS00001003964
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Memory-like HCV-specific CD8+ T cells retain a chronic scar after cure of chronic HCV infection
Study
EGAS00001004538
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Identification of the mutational consequences of precancerous liver disease (including alcohol abuse) on the genomes of human adult stem cells.
Study
EGAS00001002983
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Mutational Signature and Transcriptomic Classification Analyses as the Decisive Diagnostic Tools for a Cancer of Unknown Primary with Neuroendocrine Differentiation
Study
EGAS00001003026
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Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Study
EGAS00001005235