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• Data access committee handling data access requests for biomarker data from the clinical trial IMmotion150.

  Dac EGAC00001000946

• Data access policy for PDTX Breast Cancer RNA-seq data from Ros et al (2020)

  Dac EGAC00001001620

• DAC for "Detection of Gene Fusions using Targeted Next-Generation Sequencing – a Comparative Evaluation"

  Dac EGAC00001001905

• Data Access Committee for study Genetics of Preeclampsia at High Altitudes

  Dac EGAC00001002097

• DAC for YCC Sarcoma

  Access can be granted by contacting Hyo Song Kim (hyosong77@yuhs.ac).

  Dac EGAC50000000046

• DAC Endoresist

  Data access committee for the Endoresist project of panel sequencing: Professor Johan Hartman

  Dac EGAC50000000174

• CReATe Fertility Centre DAC

  DAC for the management of dataset own by CReATe Fertility Centre.

  Dac EGAC50000000646

• Human glioblastoma single cell DAC (Linnarsson)

  DAC for human glioblastoma single cell sequencing samples

  Dac EGAC50000000575

• Human developing meninges single cell DAC (Linnarsson)

  DAC for human developing meninges single cell sequencing

  Dac EGAC50000000576

• Asan Medical Center Data Access Committee

  Asan Medical Center Data Access Committee for BRISK study.

  Dac EGAC50000000733

• Hepatocellular Carcinoma Spatial transcriptomics Data Access Committee

  This is the DAC for study ST HCC

  Dac EGAC50000000635

• Pan Prostate Cancer Group Data Access Control Committee

  DACC for the PanProstate Cancer Group projects

  Dac EGAC50000000602

• DAC SysMed

  Data access control for datasets submitted by SysMed

  Dac EGAC50000000089

• MOSAIC Window DAC

  Data Access Committee for the MOSAIC Window initiative.

  Dac EGAC50000000398

• DAC for Genetic and Microenvironmental Analysis of PTCL at Department of Hematology, University of Tsukuba

  Dac EGAC50000000600

• DAC for "H3K27me3-mediated epigenetic repression regulates neuroblastoma development and contributes to biological heterogeneity"

  Dac EGAC00001003620

• CD3 bispecific antibody-induced cytokine release is dispensable for cytotoxic T cell activity

  Study EGAS00001003734

• Circulating tumor cells for comprehensive and multiregional non-invasive genetic characterization of multiple myeloma

  Study EGAS00001004288

• A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome

  Study EGAS00001006280

• EGAD00010000052

  Monozygotic twins that are discordant for schizophrenia (Genotyping)

  Dataset EGAD00010000052

• EGAD00000000027

  eQTL data for European newborns

  Dataset EGAD00000000027

• Exome reads

  Exome sequencing for 2 infertile brothers

  Dataset EGAD00001003193

• Exome data for PDXs

  Exome data of PDX models.

  Dataset EGAD00001001863

• WGS dataset for Genomic rearrangements in Pediatric Cancer

  Dataset EGAD00001008272

• Deep sequencing analysis of human iPSC-specific SNVs in donor cell population

  CR products were obtained from each target loci using genomic DNA from human iPS cells. Subsequently, PCR products are pooled and subjected to Illumina library preparation. The library will be sequenced either by HiSeq or MiSeq. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/

  Dataset EGAD00001000605

• Subclonal analysis in S7RE2 and S7RE14 iPS cells

  PCR products were obtained from each target loci using genomic DNA from human iPS cells. Subsequently, PCR products are pooled and subjected to Illumina library preparation. The library will be sequenced either by HiSeq or MiSeq. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/

  Dataset EGAD00001000608

• Validation of SNVs found by Exome-seq in S2-SF1, -SF5 and -SF9 hiPSCs

  PCR products were obtained from each target loci using genomic DNA from human iPS cells. Subsequently, PCR products are pooled and subjected to Illumina library preparation. The library will be sequenced either by HiSeq or MiSeq. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/

  Dataset EGAD00001000631

• Dataset for urologic_cancer-RNA

  Rare cancer sequencing data of 75 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired

  Dataset EGAD00001008851

• Dataset for soft_tissue_tumor-EXON

  Rare cancer sequencing data of 246 runs in tumor/control pairs, which were uploaded to umbrella studies. The sequencing was always paired

  Dataset EGAD00001008897

• WXS and RNA-seq raw sequence data for TG project

  WXS sequence data from 112 samples, RNA-seq sequence data from 117 samples, all sequence data are raw sequence data in fastq format, sequenced by Illumina platform.

  Dataset EGAD00001007989

• CHILD Study Dataset

  This data set contains the CRAM files for the samples in the CHILD cohort, sequenced on the Illumina HiSeq X platform.

  Dataset EGAD00001009710

• Genetics of gene expression in primary human immune cells Data Access Committee

  Dac EGAC00001003318

• Genetics of gene expression in primary human immune cells Data Access Committee

  Dac EGAC00001003327

• Longitudinal DNA methylation in the Lothian Birth Cohorts of 1921 and 1936

  Dac EGAC00001000218

• Associations between APOE and cognitive ability in Generation Scotland.

  Dac EGAC00001000332

• MeDIP-seq data in the Peri/postnatal Epigenetics Twins Study (PETS)

  Dac EGAC00001000596

• GWAS data (Illumina 2.5 M SNPs) in Cuban cohorts of dengue disease

  Dac EGAC00001000601

• Presence of fungal infection in brains of patients with Parkinson's disease (PD).

  Dac EGAC00001001199

• DKFZ Heidelberg - Genome Instability in Tumors

  Dac EGAC00001002855

• Expression quantitative trait loci influence DNA damage-induced apoptosis in cancer

  Dac EGAC50000000430

• Panic study

  To manage Panic saliva microbiota 16S data produced in collaboration.

  Dac EGAC50000000408

• Mitochondrial DNA (mtDNA) analyses in patients with schizophrenia and healthy control individuals

  Study EGAS00001003269

• Mechanisms of active DNA demethylation in human monocytes

  Study EGAS00001004784

• Quantitative Exploratory Proteomics Analysis of Glioblastoma in Initial and Recurrent Tumors

  Study EGAS00001006395

• Targetable ERBB2 Mutations in Neurofibroma/Schwannoma Hybrid Nerve Sheath Tumors

  Study EGAS00001003776

• Activating AKT1 and PIK3CA mutations in metastatic castration-resistant prostate cancer

  Study EGAS00001004328

• Atrial appendage miRNA-seq in non-, paroxysmal and persistent atrial fibrillation

  Study EGAS00001005296

• Human gut microbiome in babies with biliary atresia and normal controls

  Study EGAS00001005350

• Myeloid cell programming in patients with non-medullary thyroid carcinoma

  Study EGAS00001005594

• PIK3CA mutation in a case of CTNNB1 mutant sinonasal glomangiopericytoma

  Study EGAS00001005653