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McGill EMC Community projects Release 7 for cell line "SaOS-2"
Dataset
EGAD00001007678
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Sequencing data for oesophageal and related samples - Nowicki-Osuch, Zhuang et al (bulk RNA)
Dataset
EGAD00001005388
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NIHR BioResource Rare Diseases WGS project - Neuropathic Pain Disorders (NPD) Rare Disease domain
Dataset
EGAD00001004516
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BLUEPRINT release August 2015, DNase-Hypersensitivity for alternatively activated macrophage, on genome GRCh38
Dataset
EGAD00001001545
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WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB10_M
Dataset
EGAD00001001696
-
Single-cell TCR sequencing of DQ2.2-glut-L1-specific T cells
Dataset
EGAD00001005047
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BLUEPRINT release August 2016, DNase-Hypersensitivity for alternatively activated macrophage, on genome GRCh38
Dataset
EGAD00001002481
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Sequencing files for "A Unifying Paradigm for Transcriptional Heterogeneity and Squamous Features in Pancreatic Ductal Adenocarcinoma."
Dataset
EGAD00001005519
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cfMeDIP data for 30 CPC-GENE samples
Dataset
EGAD00001007972
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Whole exome sequencing files for St. Jude Clinical Pilot
Dataset
EGAD00001004287
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WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB55_C
Dataset
EGAD00001001766
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FFPE CRC sequence data and somatic variants
Dataset
EGAD00001007723
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BLUEPRINT release August 2016, RNA-Seq for macrophage - T=6days LPS, on genome GRCh38
Dataset
EGAD00001002337
-
Whole Exome PC9 and A375 (2019-04-03)
Dataset
EGAD00001004891
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Whole-exome/genome sequencing of childhood acute leukemia in Iraq
Dataset
EGAD00001007873
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Sequencing Data for Sample 51_Hf01_BlCM_Ct
Dataset
EGAD00001002255
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Genome and transcriptome sequence data from a liposarcoma patient
Dataset
EGAD00001002541
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WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB44_F
Dataset
EGAD00001001752
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TN
Dataset
EGAD00001003351
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Whole-exome sequencing of rare autoimmune-related phenotypes
Dataset
EGAD00001000408
-
Human tumor single-cell
Dataset
EGAD00001005129
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Reliable detection of somatic mutations in single DNA molecules
Dataset
EGAD00001006595
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Genome and transcriptome sequence data from a liposarcoma patient
Dataset
EGAD00001003060
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Genomic characterization (through whole-exome sequencing) of bone marrow clonal plasma cells before and after VRD treatment from multiple myeloma patients.
Dataset
EGAD00001006302
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NGS-ProToCol prostate cancer RNA-seq data.
Dataset
EGAD00001004215
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BLUEPRINT release August 2014, DNase-Hypersensitivity for CD34-negative, CD41-positive, CD42-positive megakaryocyte cell
Dataset
EGAD00001000942
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Whole genome sequencing on HiSeq platform of tumour-normal sample pairs from 67 mucosal melanoma cases
Dataset
EGAD00001004409
-
Whole genome sequencing on HiSeq platform of melanocytic nevi and normal sample pairs from 14 cases
Dataset
EGAD00001004474
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: MW52_M
Dataset
EGAD00001001843
-
Sequencing data for Hepatoblastoma samples
Dataset
EGAD00001006621
-
NIHR BioResource Rare Diseases WGS project - Primary Membranoproliferative Glomerulonephritis (PMG) Rare Disease domain
Dataset
EGAD00001004517
-
WGS of 50 Intellectual Disability (ID) trios with Complete Genomics Sequencing. Dataset of sample: BvB10_C
Dataset
EGAD00001001694
-
Whole Genome Sequencing of hiPS cells
Dataset
EGAD00001000362
-
scATAC sequencing of FACS sorted CD4+ T and CD25+ T from isolated tissues
Dataset
EGAD00001006779