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High Resolution Maps of the HeLa 3D Genome Using Hi-C
Study
phs001010
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PD-1 antibody-bound progenitor-exhausted CD8+ T cells in lymph nodes boost PD-1-blockade anti-tumor immunity in gastrointestinal cancer
Study
JGAS000720
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Deciphering craniopharyngioma subtypes: Single-cell analysis of tumor microenvironment and immune networks
Study
JGAS000722
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Single Cell Transcriptional Analysis of Human Adenoids Identifies Molecular Features of Airway Microfold Cells
Study
phs004103
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WGS analysis of Japanese liver cancer
Study
JGAS000151
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Parent-of-origin dependent DNA methylation and gene expression in the human placenta
Study
JGAS000038
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The genomic landscape of relapsed infant and childhood KMT2A-rearranged acute leukemia
Study
EGAS00001008197
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EATL-II STUDY
Study
EGAS00001001879
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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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GEenetic landscape of hypodiploid acute lymphoblastic leukemia
Study
EGAS00001000380
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Whole genome sequencing data for 10 hepatocellular carcinomas (HCC) and matched non-tumor liver tissues + optical mapping data for 4 HCC and 3 matched non-tumor liver tissues.
Study
EGAS00001005629
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Genetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Study
EGAS00001002182
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miR-200-regulated CXCL12β promotes fibroblast heterogeneity and immunosuppression in ovarian cancers
Study
EGAS00001002184
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DONSON encodes a novel replication fork protection factor mutated in microcephalic dwarfism.
Study
EGAS00001002224
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Whole-Genome Sequencing of a Healthy Aging Cohort.
Study
EGAS00001002306
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Orthotopic Patient-Derived Xenografts of Pediatric Solid Tumors
Study
EGAS00001002528
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DNA methylation and transposable element landscapes define human regulatory T cells in tissues and identify their blood recirculating counterpart
Study
EGAS50000000738
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Early evolutionary branching across spatial domains predisposes to clonal replacement under chemotherapy in neuroblastoma
Study
EGAS00001007650
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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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MethylBERT enables read-level DNA methylation pattern identification and tumour deconvolution using a Transformer-based model
Study
EGAS50000000806
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Whole_genome_sequencing_in_a_multiplex_Crohn_s_disease_family
Study
EGAS00001000060
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single cell sequencing of resting and Influenza-stimulated mononcluear phagocytes of African and Europeans with varying degree of ex-vivo susceptibility to Influenza
Study
EGAS00001005000
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Motif-directed chromatin repression by BCL11B shapes ectopic targeting and lineage commitment
Study
EGAS50000001719
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Monosomy 7 delineates a primitive acute myeloid leukemia with adverse prognosis and responsiveness to epigenetic therapy
Study
EGAS50000001641
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STimage: Robust and interpretable prediction of gene markers and cell types from spatial transcriptomics data
Study
EGAS50000001503