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Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
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Infant Glioma Molecular Subtype
Study
EGAS00001003714
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CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
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Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
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Myelodysplastic cells in patients re-program mesenchymal stromal cells to establish a transplantable stem cell-niche disease unit.
Study
EGAS00001000716
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Whole exome sequencing for gallbladder cancer in Xinhua Hospital Affiliated to Shanghai Jiao Tong University, School of Medicine
Study
EGAS00001000853
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Origins and functional consequence of somatic mitochondrial DNA mutations
Study
EGAS00001000968
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Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
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Single cell transcriptomic analysis of the immune cell compartment in the human small intestine and in Celiac disease
Study
EGAS00001003751
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Immune-awakening revealed by peripheral T cell dynamics after one cycle of immunotherapy
Study
EGAS00001004043
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Patient-Derived Lung Cancer Organoid
Study
EGAS00001003786
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A Genomic History of Aboriginal Australia
Study
EGAS00001001766
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Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Study
EGAS00001003822
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Comparing nodal versus bony metastatic spread using tumour phylogenies
Study
EGAS00001001801
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EATL-II STUDY
Study
EGAS00001001879
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SG10K_Pilot - Large-scale whole-genome sequencing of three diverse Asian populations in Singapore
Study
EGAS00001003875
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Inactivation of TGFβ receptors in stem cells drives cutaneous squamous cell carcinoma - 30 whole exomes
Study
EGAS00001001892
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Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
Study
EGAS00001001916
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Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Study
EGAS00001001940