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Targeted_sequencing_of_embryonic_variants___Warm_Autopsy
Study
EGAS00001003952
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Molecular classification improves risk assessment in adult B-lineage ALL: Patients on the international UKALLXII-ECOG2993 trial.
Study
EGAS00001004638
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Whole genome sequencing of EBV Associated Nasopharyngeal Carcinoma
Study
EGAS00001004705
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Single Cell ATAC-Seq on human cord-blood derived HSPC.
Study
EGAS00001004740
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Pan-neuroblastoma analysis reveals age- and signature-associated driver alterations
Study
EGAS00001003931
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Germline SDHB-inactivating mutation in gastric spindle cell sarcoma (HIPO-021)
Study
EGAS00001004277
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Coding and non-coding drivers of mantle cell lymphoma identified through exome and genome sequencing
Study
EGAS00001004289
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Prime editing for functional repair in patient-derived disease models
Study
EGAS00001004611
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Bulk ATAC-Seq on sorted cord blood hematopoietic populations
Study
EGAS00001004742
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Targeting AXL Kinase Uniquely Sensitizes Therapy-Insensitive Leukemic Stem and Progenitor Cells to Venetoclax Treatment in Acute Myeloid Leukemia
Study
EGAS00001004663
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Hi-C on the OCIAML-2 Cell Line
Study
EGAS00001004743
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Low-C on Human CB-derived LT-HSC and ST-HSC
Study
EGAS00001004744
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ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line
Study
EGAS00001004741
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Genomics-based personalized oncology in cancer of unknown primary (CUP, project H021)
Study
EGAS00001004786
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Whole exome sequencing identifies clinically relevant mutational signatures in resected hepatocellular carcinoma
Study
EGAS00001004371
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Non-coding mutations reveal cancer driver cistromes in luminal breast cancer
Study
EGAS00001005235
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Adult-type Granulosa Cell Tumour of the Ovary
Study
EGAS00001005414
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Characterization of DLBCL with a PMBL gene expression signature
Study
EGAS00001005057
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Single-cell landscapes of primary glioblastomas and matched organoids and cell lines reveal variable retention of inter- and intra-tumor heterogeneity
Study
EGAS00001005227
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SmMIP-tools:a computational toolset for processing and analysis of single-molecule molecular inversion probes derived data
Study
EGAS00001005359
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Identifying transcriptional programs underlying anti-EGFR small molecule response and resistance with TraCe-seq
Study
EGAS00001005405
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Germline variants in patients with rare cancers and their implications for precision cancer medicine: experiences from the Multicenter MASTER Trial by the German Cancer Consortium (HIPO_021)
Study
EGAS00001005537
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WGS_of_healhy_mesothelial_cells_and_primary_mesothelima_cell_lines
Study
EGAS00001005559
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Defining structural variation associated with breast cancer susceptibility by long-read genome sequencing
Study
EGAS00001005872
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Multi-omic Profiling of Central Nervous System Leukemia Identifies mRNA Translation as a Therapeutic Target
Study
EGAS00001005647