22958 results for "ega"

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• 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

• Indel/point mutation of chondrosarcoma

  Indel/point mutation of chondrosarcoma

  Dataset EGAD00001000874

• 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

• WXS of 3 samples

  WXS of 3 samples

  Dataset EGAD00001004994

• Illumina_WGS_BL

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

  Dataset EGAD00001002082

• Swedish schizophrenia patients

  The genomic sequence of brain expressed miRNA genes was sequenced in Swedish schizophrenia patients

  Dataset EGAD00001001849

• 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

• PCa RNASeq data

  RNASeq data from paired malignant/benign prostate tissues

  Dataset EGAD00001005931

• OT2_Illumina_WXS_BL

  Whole-exome sequencing on Illumina HiSeq2000/2500 of Blood EDTA (OT2_cohort)

  Dataset EGAD00001003377

• BCL2 Break NegativeFollicular Lymphoma

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

  Dataset EGAD00001003509

• PRECISION WES

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

  Dataset EGAD00001009639