23083 results for "ega"

in 52.60 milliseconds.

• Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Stockholm, Sweden (Pedersen)

  Study EGAS00001005856

• Study of renal cancers and renal cancer metastases

  Study EGAS00001001176

• The BAF chromatin remodeling complex is a novel target of spliceosome dysregulation in SF3B1-mutated chronic lymphocytic leukemia

  Study EGAS00001006771

• Elucidating the heterogeneity of immunotherapy response and immune-related toxicities by longitudinal ctDNA and immune cell compartment tracking in lung cancer

  Study EGAS00001007291

• Integrative genomic analyses of European intrahepatic cholangiocarcinoma: new ROS1 fusion gene and PBX1 as prognostic marker

  Study EGAS00001007525

• DAC for Hematological toxicity following CAR-T cells injection

  Data access committee to have access to Hematological toxicity following CAR-T cells injection

  Dac EGAC50000000490

• Cardiac fibroblast DAC

  DAC for reviewing requests to access data on cardiac fibroblasts as described by Aguado-Alvaro et al (Nature Communications, 2025)

  Dac EGAC50000000479

• BCR-HGBCL-DH-BCL2 project DAC

  Data Access Committee for high-grade B cell lymphomas MYC-BCL2 datasets

  Dac EGAC50000000500

• Liquid Biopsy High Grade Serous Ovarian Cancer WGS

  Liquid Biopsy High Grade Serous Ovarian Cancer WGS.

  Dataset EGAD50000001520

• Therapy and RNA group Ghent DAC

  This is a Data Access Committee for datasets of the Therapy and RNA group Ghent (TaRGeT, Belgium).

  Dac EGAC50000000491

• Trained immunity DNA methylation data

  This dataset contains the DNA methylation data of 904 samples from Dutch healthy individuals.

  Dataset EGAD00010002738

• Preoperative ipilimumab plus nivolumab in locoregionally advanced urothelial cancer (NABUCCO Cohorts 1 and 2)

  Study EGAS00001004521

• CeDNN Data Access Committee UMCG

  Celiac Disease Northern Netherlands cohort, set up by the Genetics department of the University Medical Center Groningen (UMCG).

  Dac EGAC50000000584

• HDBR exome sequencing data (August 2024)

  Exome sequencing data from fourteen phenotypically abnormal human fetal samples.

  Dataset EGAD50000000722

• HDBR exome sequencing data (December 2024)

  Exome sequencing data from sixteen phenotypically abnormal human fetal samples.

  Dataset EGAD50000001809

• Whole Exome Sequencing of Bipolar cases and matched controls performed at the Broad Institute on a cohort from Cardiff, UK (Owen)

  Study EGAS00001005855

• Small Intestine Adenocarcinoma Subtyping Data Access Committee

  DAC created for the Molecular classification of small intestinal adenocarcinomas Study in Amsterdam UMC.

  Dac EGAC50000000663

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

  Study EGAS00001007469

• HNSCC Patients Treated with Immune Checkpoint Blockade

  HNSCC Patients Treated with Immune Checkpoint Blockade

  Study EGAS50000001175

• Kinomics data

  To ellucidate protein activity in mRCC, Kinomics data was generated as part of the EuroTarget study

  Dataset EGAD50000002293

• Study of PD-1 negative CD8 effector T-cells in advanced HCC with single-cell sequencing

  Study EGAS00001007547

• Genome-wide DNA Methylation Analysis Reveals a Unique Methylation Pattern for Pleural Mesothelioma Compared to Healthy Pleura and Other Lung Diseases

  Study EGAS00001007783

• Chordoma_Extension_Study

  Extension analysis to pursue candidate genes of interest in chordoma

  Study EGAS00001000892

• Chordoma_Extension__known_cancer_genes_

  Extension analysis to pursue candidate genes of interest in chordoma

  Study EGAS00001000895

• Giant congenital nevi exome sequencing

  Characterization of the genomic landscape of giant congenital nevi.

  Study EGAS00001004541

• Very short reads file for testing purposes

  Very short FASTQ reads file for testing purposes

  Study EGAS00001001701

• Kidney_tumour_DNA_exome

  This is an exome DNA sequencing study of human renal tumours

  Study EGAS00001003616

• TST170 Pilot RNA BAM

  TST170 Pilot RNA BAM files

  Dataset EGAD00001006044

• ADAPTeR Study: RNAseq data from ccRCC patients

  RNAseq from tumour, mets, and PEACE study

  Study EGAS00001005637

• WGS

  Whole-genome sequencing of pancreatic cancer organoids and matched germline controls.

  Study EGAS00001007211

• DLBCLR

  Evaluating gene expression in DLBCL using a quantitative nuclease protection assay

  Study EGAS00001007479

• SNP array ARID1B patients

  SNP array ARID1B patients. Data from PBMCs and iPSCs.

  Study EGAS00001007381

• Brain mets discovery cohort variant calls

  These are the variant calls for the 50 brain tumour samples in the discovery cohort.

  Dataset EGAD00001005982

• RNAseq data

  RNAseq data for 10 patients: 10 tumors and 10 cell lines

  Dataset EGAD00001002691

• G_WTS_001 data

  RNA-seq data from Korean CRC samples

  Dataset EGAD00001006985

• Neurodegenerative_TGS

  An investigation of clonal haematopoiesis in patients with neurodegenerative disease.

  Dataset EGAD00001006392

• PRECISION WES

  WES dataset obtained using Illumina HiSeq 2500, Swift Bioscience library kit, paired reads.

  Dataset EGAD00001009639

• WXS of 3 samples

  WXS of 3 samples

  Dataset EGAD00001004994

• Whole-genome sequencing

  Whole-genome sequencing (WGS) data.

  Dataset EGAD00001008778

• 36 mouse plasma cell-free DNA cases

  36 mouse plasma cell-free DNA cases

  Dataset EGAD00001008810

• Retinal Dystrophy Dataset

  Dataset form patines with retinal dystrophies.

  Dataset EGAD00001007755

• HiChIP fastq files

  HiChIP experiments with two sequencing libraries each. Illumina HiSeq 4000/2500.

  Dataset EGAD00001006278

• Hessequa-descendants mitogenomes

  Complete sequence of the mitochondrial DNA of 87 Hessequa-descendant individuals

  Dataset EGAD00001007676

• RNA-Seq data for Juvenile Pilocytic Astrocytomas

  RNA-Seq data for 9 JPA samples.

  Dataset EGAD00001009043

• Bulk RNAseq

  Bulk RNAseq from 183 premalignant gastric biopsies

  Dataset EGAD00001010131

• Indel/point mutation of chondrosarcoma

  Indel/point mutation of chondrosarcoma

  Dataset EGAD00001000874

• WGS and WXS files for Dyer ATRX study

  WGS and WXS files for Dyer ATRX study

  Dataset EGAD00001003389

• BCL2 Break NegativeFollicular Lymphoma

  Whole Exome Sequencing reads consisting of BAM paired end reads from Follicular Lymphoma samples.

  Dataset EGAD00001003509

• Exome sequencing VCF files for glioma progression

  Exome sequencing VCF files describing mutations during glioma progression.

  Dataset EGAD00001001887

• Illumina_WGS_BL

  Whole-genome sequencing on Illumina HiSeq2000/2500 of Blood EDTA

  Dataset EGAD00001002082