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• Transcriptome of (monocytes and dendritic cells ), from donor S13, replicate 2 control

  Dataset EGAD00001009031

• Transcriptome of (monocytes and dendritic cells ), from donor S12, replicate 1 patient

  Dataset EGAD00001009028

• Transcriptome of (monocytes and dendritic cells ), from donor S11, replicate 2 patient

  Dataset EGAD00001009027

• Transcriptome of (monocytes and dendritic cells ), from donor S11, replicate 1 patient

  Dataset EGAD00001009026

• Transcriptome of (monocytes and dendritic cells ), from donor S10, replicate 2 control

  Dataset EGAD00001009025

• Transcriptome of (monocytes and dendritic cells ), from donor S10, replicate 1 control

  Dataset EGAD00001009024

• Transcriptome of (monocytes and dendritic cells ), from donor S9, replicate 2 control

  Dataset EGAD00001009023

• Transcriptome of (monocytes and dendritic cells ), from donor S9, replicate 1 control

  Dataset EGAD00001009022

• Transcriptome of (monocytes and dendritic cells ), from donor S8, replicate 2 patient

  Dataset EGAD00001009021

• Transcriptome of (monocytes and dendritic cells ), from donor S8, replicate 1 patient

  Dataset EGAD00001009020

• Transcriptome of (monocytes and dendritic cells ), from donor S7, replicate 2 patient

  Dataset EGAD00001009019

• Transcriptome of (monocytes and dendritic cells ), from donor S7, replicate 1 patient

  Dataset EGAD00001009018

• Transcriptome of (monocytes and dendritic cells ), from donor S6, replicate 2 control

  Dataset EGAD00001009017

• Transcriptome of (monocytes and dendritic cells ), from donor S6, replicate 1 control

  Dataset EGAD00001009016

• Transcriptome of (monocytes and dendritic cells ), from donor S5, replicate 2 control

  Dataset EGAD00001009015

• Transcriptome of (monocytes and dendritic cells ), from donor S5, replicate 1 control

  Dataset EGAD00001009014

• Transcriptome of (monocytes and dendritic cells ), from donor S4, replicate 2 patient

  Dataset EGAD00001009013

• Transcriptome of (monocytes and dendritic cells ), from donor S4, replicate 1 patient

  Dataset EGAD00001009012

• 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

• Targeted Sequencing Xenturion

  Targeted sequencing of a biobank of PDOs PDXs and LMHs

  Dataset EGAD00001009653

• 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

• Somatic L1 retrotransposition dynamics in high-grade serous ovarian cancer

  Somatic L1 retrotransposition was mapped in high-grade serous carcinoma (HGSC) tumors using LDI-PCR/Nanopore-seq method. This method identifies somatic L1 insertions originating from two active L1 loci at chr22q12.1 and chrXp22.2. Multiple tumors from same patient were utilised to understand L1-mediated intrapatient heterogeneity.

  Study EGAS50000001198

• 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

• Identification of causal mutation in two patients with Sotos Syndrome Features

  We performed whole exome sequencing (WES) on genomic DNA derived from two patients with Sotos Syndrome Features. Sequencing (100 base pair paired-end) was performed on an Illumina Hiseq 2000 sequencer after enrichment of 62Mb of exonic and adjacent intronic sequences with TruSeq Exome Enrichment Kit (Illumina, San Diego, CA, USA).

  Study EGAS00001000993

• Multifocal Breast Project

  Comparison of genomic rearrangements and DNA methylation patterns between different foci of multiple synchronous (multifocal and multicentric) invasive breast cancers.

  Dataset EGAD00001001041

• WGS of multi-centric liver cancers and intra-haptatic metastasis of liver cancer.

  RIKEN collection of WGS read of 59 multi-centric liver cancers or intra-haptatic metastasis and matched blood samples from 19 donors.

  Dataset EGAD00001001643

• 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

• 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

• 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

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

  Dataset EGAD00001005526

• 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

• Osteosarcoma exome sequencing dataset

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

  Dataset EGAD00001002145

• ORIENT study

  scRNAseq dataset containing 5 healthy donors and 4 asthmatic donors.

  Dataset EGAD00001009687

• Comprehensive Characterization of Early Relapse and End-Stage Relapsed Refractory Multiple Myeloma (HIPO K08K/H067/H021+nonHIPO)

  Study EGAS00001007469

• 20210708_EGA_Melanoma_mk2 WGS 570 donors

  Illumina platform whole genome sequencing data for matched tumour-normal DNA samples from 570 melanoma patients

  Dataset EGAD00001008798

• MDS PacBio LRTS IsoSeq

  This dataset contains long read transcriptome sequencing of 25 myelodysplastic sndrome (MDS) patients with or without mutation in SF3B1. The BAM files are unaligned CCS reads.

  Dataset EGAD50000000077

• RNA sequencing

  RNAseq of 45 high-grade serous ovarian cancer tumour samples. Libraries were generated using the NEB Ultra II Directional RNA library Prep kit with polyA enrichment. Libraries were sequenced as paired-end 50 or 100bp on an Illumina NextSeq or NovaSeq.

  Dataset EGAD00001009844

• 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