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Human induced pluripotent stem cells display a similar mutation burden as embryonic pluripotent cells in vivo
Study
EGAS00001005939
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Transcriptome analysis in very preterm infants with chronic lung disease after birth
Study
EGAS00001002586
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Epigenomic alterations define lethal CIMP-positive ependymomas of infancy
Study
EGAS00001000443
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Whole-exome ultra-high throughput sequencing in brain samples of suicide victims who had suffered from major depressive disorder and control subjects who had died from other causes
Study
EGAS00001002818
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Single-cell RNA-seq of cervix and placenta
Study
EGAS00001007044
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MGA-NUTM1 fusion in high grade spindle cell sarcoma
Study
EGAS00001003341
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Biallelic DICER1 mutations in sporadic pleuropulmonary blastoma
Study
EGAS00001000662
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Inferring expressed genes by whole-genome sequencing of plasma DNA
Study
EGAS00001001754
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Genomic analyses of gynecologic carcinosarcomas reveal frequent mutations in chromatin remodeling genes
Study
EGAS00001000941
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Epigenomics and Single-cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
Study
EGAS00001003822
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Translation of non-canonical open reading frames as a cancer cell survival mechanism in childhood medulloblastoma
Study
EGAS00001007426
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SG10K_Pilot - Large-scale whole-genome sequencing of three diverse Asian populations in Singapore
Study
EGAS00001003875
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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
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HCA_Gonads_Foetal_EU_H2020_HUGODECA_RNA
Study
EGAS00001004723
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Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
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Clinical Implications of Genomic Alterations in the Tumor and Circulation of Pancreatic Cancer Patients
Study
EGAS00001001257
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Spatial genomic heterogeneity in multiple myeloma revealed by multi- region sequencing
Study
EGAS00001002111
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Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
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Genome analysis of oesophageal cancer and Barrett's oesophagus
Study
EGAS00001002864
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Novel mutational mechanisms and drivers in Pancreatic Neuroendocrine Tumours
Study
EGAS00001001732
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A Genomic History of Aboriginal Australia
Study
EGAS00001001766
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Comparing nodal versus bony metastatic spread using tumour phylogenies
Study
EGAS00001001801
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Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015
Study
EGAS00001001570
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Tracking the genomic evolution of esophageal adenocarcinoma through neoadjuvant chemotherapy
Study
EGAS00001001254