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Heterogeneous metabolic signatures are linked to cancer cell differentiation in colorectal cancer
Dataset
EGAD00001005524
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Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells
Dataset
EGAD00001007997
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Single-cell RNA-seq of peripheral blood mononuclear cells in classic Hodgkin lymphoma
Dataset
EGAD00001011360
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Colorectal cancer organoid-stroma biobank cohort
Dataset
EGAD00001011173
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An integrated single-cell reference atlas of the human endometrium
Dataset
EGAD00001015446
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Follicular lymphoma shallow whole genome sequencing and targeted sequencing of lymphoma panel
Dataset
EGAD00001008385
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RNA sequencing in primary inflammatory (TPP) macrophages treated with a MEK1/2 inhibitor
Dataset
EGAD00001011337
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Identification of rare variants associated with cardiovascular traits in Cilento isolates
Dataset
EGAD00001002195
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WGS short read and 10X linked read sequencing of HR Deficient breast cancers
Dataset
EGAD00001010326
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Single-cell RNA sequencing on 11,138 single T cells from 12 colon and rectal cancer (CRC) patients
Dataset
EGAD00001003910
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Genomic alterations in MM - BAM
Dataset
EGAD00001004117
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Whole Genome Sequencing of Liver Cancers
Dataset
EGAD00001003281
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Identifying autosomal recessive mutations causing neurological disorders
Dataset
EGAD00001000340
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Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: KARE
Study
phs001096
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Ashkenazi
Study
phs001095
-
Type 2 Diabetes Genetic Exploration by Next-Generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: Singapore
Study
phs001097
-
Type 2 Diabetes Genetic Exploration by Next-generation Sequencing in Multi-Ethnic Samples (T2D-GENES) Project 1: London Life Sciences Population Study (LOLIPOP) UK South Asian
Study
phs001093
-
Rare Genetic Steroid Disease Consortium (GSD) Apparent Mineralocorticoid Excess (AME) Syndrome Natural History Clinical Protocol
Study
phs000603
-
Genetic Causes of Congenital Anosmia
Study
phs003328
-
All you need to know about the new Submitter Portal
Blog
new-submitter-portal
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Molecular_characterization_of_invasive_lobular_carcinoma
Study
EGAS00001000292
-
GCAT| WGS Imputation Panel V1
Dataset
EGAD00010002153
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Expression array
Dataset
EGAD00010002596
-
Whole genome sequencing of Sinonasal hemangiopericytoma and patient derived cell line model
Study
EGAS50000000025
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RNA-Sequencing of cervical cancers
Dataset
EGAD50000000120