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• Transcriptome of (monocytes and dendritic cells ), from donor S3, replicate 2 patient

  Dataset EGAD00001009011

• Transcriptome of (monocytes and dendritic cells ), from donor S3, replicate 1 patient

  Dataset EGAD00001009010

• Transcriptome of (monocytes and dendritic cells ), from donor S2, replicate 1 control

  Dataset EGAD00001009008

• Transcriptome of (monocytes and dendritic cells ), from donor S1, replicate 2 control

  Dataset EGAD00001009007

• Transcriptome of (monocytes and dendritic cells ), from donor S1, replicate 1 control

  Dataset EGAD00001009006

• Transcriptome of (monocytes and dendritic cells ), from donor S2, replicate 2 control

  Dataset EGAD00001009009

• Exome sequencing of nine PCC/PGL tumors

  Exome sequencing of nine PCC/PGL tumors, SF and FFPE samples

  Dataset EGAD00001001854

• MSI-Exome-DAC Team Microsatellites Instability and Cancer, INSERM Hospital Saint-Antoine, Paris 12, France Carte d'identité des tumeurs, French league against cancer, Paris France

  Dac EGAC00001000665

• Early on-treatment changes in circulating tumor DNA fraction and response to enzalutamide or abiraterone in metastatic castration-resistant prostate cancer - Data Access Committee

  Dac EGAC00001003128

• High throughput profiling of undifferentiated pleomorphic sarcomas identifies two main subgroups with distinct immune contexture, clinical outcome and sensitivity to targeted therapies

  Study EGAS00001004612

• Mutation and Microsatellite Burden Predict Response to PD-1 Inhibition in Children with Germline DNA Replication Repair Deficiency: An Observational Registry Study

  Study EGAS00001005579

• DNA_Methylation_450K

  BLUEPRINT DNA methylation profiles of monocytes, neutrophils and T cells from healthy donors

  Dataset EGAD00010000850

• ORIENT study

  scRNAseq dataset containing 5 healthy donors and 4 asthmatic donors.

  Dataset EGAD00001009687

• RNA-Sequencing generated from 180 human putamen and substantia nigra

  Dataset EGAD00001005526

• Osteosarcoma exome sequencing dataset

  Whole exome sequencing data of primary, secondary and tertiary tumor from a patient.

  Dataset EGAD00001002145

• RNA-seq data from diagnosis and relapse samples of Down Syndrome acute lymphoblastic leukemia.

  Dataset EGAD00001003280

• Exome sequencing of hepatocellular carcinomas identifies new mutational signatures and potential therapeutic targets

  Dataset EGAD00001001096

• Disorders of growth and insulin action

  Illumina paired-end sequencing of whole- exome pulldown DNA from Severe Insulin Resistant patients.

  Dataset EGAD00001000381

• RNA-seq analysis of BMP-stimulated glioma initiating cells

  Bone morphogenetic protein (BMP) signaling has been shown to suppress progression of glioblastoma by promoting astrocytic differentiation; however, roles of BMP signaling in cell proliferation and apoptosis of glioblastoma cells remains to be elucidated. We here performed RNA-seq analysis of glioma initiating cells to identify transcriptional target(s) of BMP.

  Study JGAS000077

• Chondrosarcoma_Targeted_Sequencing_Study

  This Study uses a focused bait pull down library method to target findings of Chondrosarcoma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these finding in a larger set of patients.

  Study EGAS00001000277

• Geographic and age-related variations in mutational processes in colorectal cancer - patient metadata files (Mutographs)

  Geographic and age-related variations in mutational processes in colorectal cancer - patient metadata files (Mutographs)

  Dataset EGAD00001015437

• Transcriptome sequencing of hepatocellular carcinoma biopsies (TACE study)

  Illumina-based RNA-Seq analysis of 93 liver samples. Biopsies of tumors and non-tumor tissues are included. Samples are stratified by response and non-response to TACE treatment.

  Dataset EGAD00001008158

• WES of blood and patient-matched cecum tumor tissue samples, Panel NGS of patient-matched cfDNA

  WES using IDT xGen Research Exome on Illumina NovaSeq 2x150bp: Normal sample (buffy coat), cecum tumor biopsy at diagnosis, ileocecal valve region tumor sample at week 19, pericolonic metastasis at week 19, lymph node metastasis at week 19, peritoneal metastasis at week 19. Week 19 samples from hemicolectomy. Deep coverage cfDNA NGS using PanCeq pan-cancer panel on NextSeq 2x150bp: week 2 and week 10.

  Dataset EGAD00001005737

• RNAseq dataset of ovarian cancer patients

  Dataset of transcriptomics data from a cohort of individuals diagnosed with ovarian cancer. This dataset includes RNAseq sequencing data from 68 individuals. A total of 109 tumor samples were sequenced. Samples were prepared with the Illumina TruSeq Stranded RNA library. Sequencing data are paired end.

  Dataset EGAD50000001556

• High-grade serous ovarian carcinoma tumour whole genome sequencing variants

  Tumour somatic variants (in VCF format) called from paired tumour-germline whole genome sequencing (using IDT library preparation system followed by sequencing on Illumina NovaSeq platform) of three high-grade serous ovarian tumour samples. The dataset comprises three VCF variant files.

  Dataset EGAD50000001131

• Whole Exome Sequencing Data of 34 indolent primary renal B-Cell lymphoma cases

  Here, 34 iNHL samples were sequenced using whole exome sequencing to describe the mutational landscape of indolent primary renal B-Cell lymphomas. Mutational profiles were compared to other Marginal Zone Lymphomas.

  Dataset EGAD50000001136

• Variants Derived From Kids Heart BioBank TOF Probands (Australia)

  Short variants identified in 245 TOF probands enrolled through the Kids Heart BioBank (Australia).

  Dataset EGAD50000000839

• Variants Derived From CONCOR Biobank TOF Probands (Netherlands)

  Short variants identified in 125 TOF probands enrolled through the CONCOR Biobank (Netherlands).

  Dataset EGAD50000000837

• Longitudinal WES data from MEMORI trial

  70 bam files generated from deep whole exome sequencing from samples from oesophageal adenocarcinoma from 17 patients. 17 bam files generated from deep whole exome sequencing from matching blood (germline control) from patients with oesophageal adenocarcinoma. Samples were collected within the clinical MEMORI trial.

  Dataset EGAD50000000355

• EBNA2 ChIP-Re-ChIP in primary B-cells infected with EBV virus

  EBNA2 ChIP-Re-ChIP in primary bulk B cells 4 days post EBV-infection with B95-8. DNA binding elements of the viral master regulator EBNA2, EBNA2-CBF transcription factor complex or EBNA2-EBF1 transcription factor complex were analyzed to identify virally targeted genes.

  Dataset EGAD50000000301

• Whole-exome sequencing of IMFT tumor samples f

  Whole-exome sequencing of IMFT tumor samples from 24 participants in the clinical phase II trial EORTC 90101 “CREATE” (CREATE IMFT cohort)

  Dataset EGAD00001007803

• CONTAGIOUS trial - COVID-19 16S dataset

  16S amplicon data of nasopharyngeal swabs in a COVID-19 cohort recruited at UZ Leuven. The dataset contains a single experiment, comprising 150 runs corresponding to 125 unique samples. Runs comprise paired fastq files (2*250 bases) obtained from an Illumina MiSeq instrument.

  Dataset EGAD00001006864

• Genomic Landscape of Radiation Induced Meningiomas

  EGAS00001002317 - Whole exome sequencing of data of 18 RIMs with matched bloods. Median depth of 112x (range of 110-120). Performed on Illumina HiSeq Platform. EGAS00001002318 - RNA sequencing data of 18 RIMs on the Illumina HiSeq Platform.

  Dataset EGAD00001004358

• Baulac Lab - Paris Brain Institute

  Raw 10X single-nucleus RNA-seq data from human postoperative brain samples of patients with epilepsy and cortical malformations.

  Dac EGAC50000000546

• Single cell sequencing reveals expanded cytotoxic CD4+ T cells and two clusters of peripheral helper T cells in synovial fluid of ACPA+ RA patients

  Study EGAS00001005241

• ILC RNAseq dataset

  RNAseq data from ILC (n=168) and IC-NST/IDC (n=79)

  Dataset EGAD50000002527

• CRISPR_perturbations_IRF4_PRDM1_Bcells

  CRISPR perturbations of IRF4, PRDM1, and AAVS1 (within PPP1R12C gene) in activated B cells

  Dataset EGAD50000002113

• DLBCL cfDNA seq

  Sequencing dataset of 290 DLBCL and HGBL cfDNA samples of paired end 150bp sequencing runs.

  Dataset EGAD50000000602

• Whole-exome sequencing of buccal mucosa samples

  40 buccal mucosa samples and a paired blood sample were whole-exome sequenced.

  Dataset EGAD50000000080

• miRNA profiling of human plucked hair follicle

  miRNA profiling of human plucked hair follicle from frontal and occipital scalp

  Dataset EGAD00010001500

• EGAD00010000450

  Genome Wide Genotype Data

  Dataset EGAD00010000450

• Medulloblastoma Illumina RNA-Seq

  Illumina RNA-sequencing of Medulloblastoma primary and relapse tumor.

  Dataset EGAD00001009425

• Medulloblastoma Illumina WGS

  Illumina whole genome sequencing of Medulloblastoma Blood, Primary tumor, and Relapse tumor

  Dataset EGAD00001009424

• Exome Sequencing of Gastric Cancer Samples

  We perform whole exome sequencing on 50 pairs of gastric cancer and matched normal samples.

  Dataset EGAD00001006957

• Transcriptomic profiling of lymphedema

  RNA-seq of skin from human subjects with and without lymphedema

  Dataset EGAD00001006246

• Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends

  Dataset EGAD00001003778

• High-grade meningioma sequencing data

  Whole genome, whole exome, and custom panel sequencing of high-grade meningioma cohort

  Dataset EGAD00001003220

• Whole Genome Sequencing of acral melanoma

  Whole Genome Sequencing of 5 acral melanomas and matched normal samples

  Dataset EGAD00001000944

• Single-cell RNA sequencing data of human lymph node samples generated with BD Rhapsody

  The single cell data were generated based on four cartridges. The samples are multiplexed: 0. Sample Run Id Hash Gender Age 1. FL-6 Run1_C1 4 f 71 2. rLN-3 Run1_C1 6 f 72 3. DLBCL-4 Run1_C1 7 f 68 4. DLBCL-1 Run1_C1 8 m 66 5. FL-4 Run1_C1 9 m 41 6. DLBCL-3 Run1_C2 10 f 60 7. rLN-4 Run1_C2 11 f 58 8. rLN-5 Run1_C2 12 m 61 9. FL-1 Run2_C1 1 f 81 10. DLBCL-2 Run2_C1 2 m 80 11. rLN-2 Run2_C1 3 f 42 12. FL-5 Run2_C1 4 m 66 13. DLBCL-8 Run2_C1 5 m 64 14. DLBCL-6 Run2_C2 6 m 76 15. rLN-1 Run2_C2 7 m 39 16. FL-3 Run2_C2 8 f 76 17. DLBCL-5 Run2_C2 9 m 66 18. FL-2 Run2_C2 10 f 58 19. DLBCL-7 Run2_C2 11 f 71

  Dataset EGAD00001010044

• JKLab, SNU College of Medicine

  JKLab, Lab of Cellular Translational Medicine, Department of Anatomy and Cell Biology, Seoul National University College of medicine.

  Dac EGAC50000000288

• Immunopeptidomics of colorectal cancer organoids reveals a sparse HLA class I neoantigen landscape and no increase in neoantigens with interferon or MEK-inhibitor treatment

  Study EGAS00001003886

• MPNST study - LCM WGS data

  LCM WGS data from one MPNST patient, including one primary and five recurrence regions

  Dataset EGAD50000002568

• Methylation_PBL_UC_Tofacitinib

  Longitudinal whole-genome DNA methylation profiling of PBL obtained from UC patients categorized as responders and non-responders

  Dataset EGAD00010002590

• Groupe_case

  Illumina EPIC arrays of human osteoblastomas and their mimics

  Dataset EGAD00010002279

• Whole transcriptome and 850k methylome profiling of human MBM

  Assessment of methylation status of ~850,000 sites

  Dataset EGAD00010002281

• Methylation_monocytes_female_CD

  Whole-genome DNA methylation profiling of CD14+ monocytes obtained from CD-active, CD-remissive and non-CD individuals

  Dataset EGAD00010001846

• Illumina_450K

  Primary renal cell carcinoma (RCC), RCC metastases and cell lines by Illumina 450K

  Dataset EGAD00010001001

• 450K_DKFZ_CLL_NB

  CLL and normal B cell samples using 450K

  Dataset EGAD00010000871

• IBC Whole exome sequencing

  Bam files of IBC whole exome sequencing, including tumor and matching normal

  Dataset EGAD00001011648

• RCRF release 1

  exome data from leiomyosarcoma, large cell neuroendocrine carcinoma, and clear cell sarcoma

  Dataset EGAD00001010197

• TCR β-chain repertoire characterization of regulatory and conventional T cells in breast tumors from breast cancer patients.

  Dataset EGAD00001006428

• Leeds GLASS Data Release 1

  Paired end Illumina whole exome sequencing of 9 GBM trios (blood, primary and recurrent tumour).

  Dataset EGAD00001004856

• 20180221_EGA_OESO

  Illumina platform sequencing of whole genome libraries prepared from normal, Barrett's oesophagus and oesophageal cancer samples from 44 donors

  Dataset EGAD00001003996

• Maastricht Irritable Bowel Syndrome metagenomic sequencing

  Metagenomic shotgun sequencing of Irritable bowel syndrome patients and matched controls

  Dataset EGAD00001002668

• Dataset of PPB

  Whole exome sequencing and miRNA-seq data of PPB.

  Dataset EGAD00001000822

• WEHI AML Multiome Committee

  This committee oversees access to data generated as part of AML research study at WEHI, ensuring compliance with privacy regulations and ethical standards.

  Dac EGAC50000000912

• ADARIO Dataset

  RNA editing analyses of BRCA-isogenic cell lines and patient-derived xenografts (PDX)

  Dataset EGAD50000000739

• Transcriptome data

  Transcriptome data of affected and controls.

  Dataset EGAD50000000466

• Stability of gut microbiome after COVID-19 vaccination in healthy and immuno-compromised individuals

  Metagenomic sequencing of human fecal samples

  Dataset EGAD50000000258

• Methylation data

  Methylation data on tumor (n=102) and normal nerve (n=7) DNA samples

  Dataset EGAD00010002441

• EPIC methylation array of human lung fibroblasts

  EPIC Array data from human lung fibroblasts isolated from fresh and cryopreserved lung tissue (16 samples, 3 donors)

  Dataset EGAD00010002463

• MB_450k_methylation

  450k methylation arrays of primary and relapse tumor of a single case of sonic hedgehog medulloblastoma with Li-Fraumeni syndrome

  Dataset EGAD00010002370

• SNParray copy number dataset

  4 oesophageal cancer derived organoid lines and 2 ovarian cancer derived organoid lines

  Dataset EGAD00010002002

• BM-eGFP+ MSC expression arrays

  original population (oMSC) and highly migrative subpopulation (sMSC) of murine eGFP+ bone marrow MSC

  Dataset EGAD00010001265

• EGAD00010000496

  Genome-wide SNP genotyping of African rainforest hunter-gatherers and neighbouring agriculturalists

  Dataset EGAD00010000496

• Carcinosarcoma Exome Sequencing Data

  Whole exome sequencing data from tumor and normal samples from carcinosarcoma (malignant mixed mullerian tumor) patients

  Dataset EGAD00001000987

• RNAseq of fibroblasts

  RNA sequencing data of fibroblasts from 3 controls and 3 patients with RBMX variants.

  Dataset EGAD50000002371

• Methylation_PBL_IBD_LTS

  Longitudinal whole-genome DNA methylation profiling of PBL obtained from IBD patients (CD and UC) at two different time points

  Dataset EGAD00010002402

• PDAC organoid genomic heterogeneity

  Two primary tumor-derived PDAC organoids were subjected to SNP array, RNA-seq, and single-cell WGS

  Dataset EGAD00010002408

• H3Africa TrypanoGEN+ Fastq

  TrypanoGEN+ data containing fastq files of 183 samples from DRC, Malawi and Uganda using NextSeq500.

  Dataset EGAD00001011666

• COVID-19 Postmortem Medulla and Olfactory Mucosa snRNA-seq

  Time-dependent characterization of CNS response in COVID-19

  Dataset EGAD00001009075

• AML exome sequencing

  Raw data (fastq files) from whole exome sequencing of AML patients (paired diagnosis and complete remission samples)

  Dataset EGAD00001002116

• Hiseq 2000 and GA whole genome sequecing of 14 paired hepatocellular carcinomas

  Dataset EGAD00001001645

• Sardinia Population SNPs frequencies

  List of SNPs, and their frequencies, extracted from a low pass whole genome sequencing of 3,514 individuals.

  Dataset EGAD00001003141

• GCP Challenges in Hepatology

  raw RNAseq data from blood plasma of patients diagnosed with liver disease. Total RNA libraries were prepared using the SMARTer Stranded Total RNA-Seq-Kit v3 - Pico Input Mammalian (Takara Bio). Libraries were paired-end sequenced (2x100) o a NovaSeq 6000 instrument using NovaSeq S2 or S1 kit (Illumina).

  Dataset EGAD50000000775

• Variants Derived From Heart Centre Biobank CHD Probands (Canada)

  Short variants identified in 731 CHD probands enrolled through the Heart Centre Biobank Registry (Canada).

  Dataset EGAD50000000838

• HiC-sequencing in human monocyte differentiation

  This dataset consists of in situ HiC-seq data from human monocytes, monocyte-derived dendritic cells as well as monocyte-derived cells that were subjected to siRNA treatment targeting CTCF or RAD21. In total, the data set includes 42 samples.

  Dataset EGAD00001007955

• Transcriptome sequencing of replication repair deficient brain cancers

  Hypermutant tumors which harbor many somatic mutations may obscure the interpretation of targetable genomic events. This dataset contains transcriptome sequencing from 21 replication repair deficient brain tumor samples as well as healthy controls.

  Dataset EGAD00001006921

• Measurable residual disease in elderly acute myeloid leukemia: results from the PETHEMA-FLUGAZA phase III clinical trial

  In our study, we hypothetyzed that CD34progenitors from cases with undetectable Minimal residual Disease (MRD) by flow cytometry would contain cells with leukemic-initiating-potential that could be identified on genetic (rather than phenotypic) grounds by Whole Exome Sequencing.

  Dataset EGAD00001006585

• WGS from PDAC samples

  Bam files from WGS of PDAC samples used in the PCSI mismatch repair study

  Dataset EGAD00001006262

• Chordoma_Targeted_Sequencing_Study

  This Study uses a focused bespoke bait pull down library method to target findings of Chordoma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Study EGAS00001000280

• Osteosarcoma_Targeted_Sequencing_Study

  This Study uses a focused bespoke bait pull down library method to target findings of Osteosarcoma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Study EGAS00001000278

• Meningioma_Targeted_Sequencing_Study

  This Study uses a focused bespoke bait pull down library method to target findings of Meningioma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Study EGAS00001000282

• Childhood Cancer Model Atlas

  we establish a single-site collection of 243 cell lines, including 207 paediatric cancer cell lines representing 14 distinct extracranial and brain childhood tumour types. We subjected 164 paediatric cancer cell lines to multi-omic analyses across three dimensions (DNA-sequencing, RNA-sequencing, DNA methylation) to classify them based on clinically relevant molecular subtypes.

  Study EGAS00001006320

• Epigenome cohort 30 Patient DNA and RNA

  This dataset includes RNA-seq, DNA and Chip-Seq data of samples from our paper.

  Dataset EGAD00001009041

• WGS and RNA-Seq data from a GBM patient PT-PR5617

  WGS and RNA-Seq data from a GBM patient PT-PR5617

  Dataset EGAD00001008525

• WGS and RNA-Seq data from a GBM patient PT-ML9537

  WGS and RNA-Seq data from a GBM patient PT-ML9537

  Dataset EGAD00001008523

• WGS and RNA-Seq data from a GBM patient PT-LC6372

  WGS and RNA-Seq data from a GBM patient PT-LC6372

  Dataset EGAD00001008522

• WGS and RNA-Seq data from a GBM patient PT-JR9883

  WGS and RNA-Seq data from a GBM patient PT-JR9883

  Dataset EGAD00001008521

• WGS and RNA-Seq data from a GBM patient PT-GI2070

  WGS and RNA-Seq data from a GBM patient PT-GI2070

  Dataset EGAD00001008520