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• PNG_GWAS-2.5M_b37_2019

  EGAS00001001311: Genome-wide study of resistance to severe malaria in eleven worldwide populations:PNG

  Dataset EGAD00010001735

• Ghana_GWAS-2.5M_b37_2019

  EGAS00001001311: Genome-wide study of resistance to severe malaria in eleven worldwide populations:Ghana

  Dataset EGAD00010001734

• Vietnam_GWAS-2.5M_b37_2019

  EGAS00001001311: Genome-wide study of resistance to severe malaria in eleven worldwide populations:Vietnam

  Dataset EGAD00010001733

• CRU303 GWAS Raw Data Batch 1 Cases

  Raw data files of samples in batch 1 of CRU303 GWAS

  Dataset EGAD00010001954

• CRU303 GWAS Raw Data Batch 2 Cases

  Raw data files of samples in batch 2 of CRU303 GWAS

  Dataset EGAD00010001952

• Raw mRNA expressions

  WG mRNA profiling in FFPE primary melanoma

  Dataset EGAD00010001562

• Multi-site tumor sampling highlights molecular intra-tumor heterogeneity in malignant pleural mesothelioma

  Dataset EGAD00001007762

• RNA-Seq of SMARCB1 re-expression and HDAC+mTOR inhibition experiments in malignant rhabdoid tumor organoids

  Dataset EGAD00001006574

• RNA-seq, WGS and WES of Hepatocellular carcinomas, enriched in fibrolamellar carcinomas

  Dataset EGAD00001005308

• Angiosarcoma follow up study

  A bespoke targeted pulldown experiment will be performed on patients with Angiosarcoma. the resulting products will be sequenced to determine the prevalence of previously found mutations in these patients.

  Dataset EGAD00001000620

• Annotation file of DNA sequencing data and response

  Annotation file of DNA sequencing data of the pre-treatment biopsies in the PRADO trial and the response outcomes of the patients

  Dataset EGAD50000002547

• MMR (DNA mismatch repair) pathway in human samples

  This data are related to the manuscript by Germano et al. Ms2016-04-06029

  Study EGAS00001002694

• Identification of cis-regulatory mutations generating de novo edges in personalized cancer gene regulatory networks

  Whole genome sequencing data on 10 human cancer cell lines

  Dataset EGAD00001003824

• GENOMIC INSTABILITY IN MISMATCH REPAIR DEFICIENT COLORECTAL CANCER WES MSI Colorectal Cancer

  This dataset contains Whole Exome Sequencing of 47 MSI colorectal cancers (CRCs) and paired adjacent normal mucosa

  Dataset EGAD00001004550

• Four lymphoma cell lines (AGO2-PAR-CLIP)

  PAR-CLIP was performed on the Argonaute-2 protein (AGO2) in four lymphoma cell lines:NamalwaRajiSU-DHL-4SU-DHL-6

  Dataset EGAD00001001468

• bam files Targeted BS

  Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015

  Dataset EGAD00001001667

• BAM Files MBD-SEQ

  Data from the paper Context-specific Effects of TGFβ/SMAD3 in Cancer Are Modulated by the Epigenome. Tufegdzic et al, Cell Reports 2015

  Dataset EGAD00001001668

• Organoid Derivation Project TGS: Release 1

  Targeted gene sequencing of cancer driver genes to determine the driver mutations present in newly-derived cancer organoid models

  Dataset EGAD00001004368

• Exome sequencing reads

  Exome sequencing reads of two UFM individuals and their family members (totally 11 individuals) belonging to two different Fragile X families. Alignment files in BAM format are provided.

  Dataset EGAD00001002276

• Whole genome SMRT sequencing in the HF-GBM-Tumor-Neurosphere-Xenograft study

  This data set consists of whole genome SMRT sequencing fastqs generated from 2 xenograft samples.

  Dataset EGAD00001002264

• Dateset of clonal evolution in myelofibrosis

  This dataset includes bam files of tumor and paired normal samples derived from 15 patients with myelofibrosis. Tumor samples includes those before and after treatment.

  Dataset EGAD00001005282

• Promoter-Capture Hi-C datasets in human islets

  4 Promoter-Capture Hi-C datasets of human pancreatic islets from 4 human islet donors

  Dataset EGAD00001005206

• subset of dataset EGAD00001002528, as used in EGAS00001004517

  linking 3 samples out of EGAD00001002528 to EGAS0001004517

  Dataset EGAD00001006263

• Panel sequencing data of IMPACT2 patients

  Patient samples were sequenced by Foundation Medicine, Inc. (Cambridge, MA), using FoundationOne CDx, a comprehensive NGS-based in vitro diagnostic device designed to capture cancer genes.

  Dataset EGAD00001006887

• Pre-neoplastic liver colonization by 11p15.5 altered mosaic cells in young children with hepatoblastoma

  Additional datasets linked to EGAS00001006692

  Dataset EGAD00001011097