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• nNGM analysis of treatment-naive MIBC and NMIBC

  nNGM analysis of treatment-naive MIBC (N=49) and NMIBC (N=16).

  Dataset EGAD00001010899

• DATA ACCESS WITH REGARDS TO EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION

  Dac EGAC00001000420

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Dac EGAC00001002145

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Dac EGAC00001002151

• UKB_Genotyped 2018

  The UK BioBank directly genotyped dataset 2018

  Dataset EGAD00010001497

• HCEMM - Semmelweis University Molecular Oncohematology Research Group DAC

  Data Access Committee of the HCEMM - Semmelweis University Molecular Oncohematology Research Group

  Dac EGAC50000000091

• HPRU in Respiratory Infections DAC

  DAC to oversee data owned from the HPRU in Respiratory Infections at Imperial College London

  Dac EGAC50000000307

• TFTAK Data Access Committee

  The TFTAK Data Access Committee (TFTAK DAC) oversees access to data generated by TFTAK research projects.

  Dac EGAC50000000885

• Molecular determinants of outcomes in relapsed mantle cell lymphoma treated with ibrutinib or temsirolimus in the MCL3001 (RAY) trial

  Study EGAS00001006342

• iMED DNA methylation data

  This dataset contains the DNA methylation data of 439 samples from iMED cohort

  Dataset EGAD00010002765

• GSA_2023_hg19

  Genopyting of 45 individuals using the Illumina Global Screening Array-24 v3

  Dataset EGAD00010002707

• GSA_2020_hg38

  Genopyting of 65 individuals using the Illumina Global Screening Array-24 v2

  Dataset EGAD00010002706

• GSA_2022_hg19

  Genopyting of 45 individuals using the Illumina Global Screening Array-24 v3

  Dataset EGAD00010002705

• The study of response to EGFR Blockade in Colorectal Cancer

  Dataset EGAD00001001628

• The study of response to EGFR Blockade in Colorectal Cancer

  Dataset EGAD00001001674

• Somatic mutations in angiosarcoma

  Here we present the genomes of three secondary angiosarcomas

  Dataset EGAD00001000735

• AML-MRD

  AML-MRD: Aligned sequences used in the error modeling study

  Dataset EGAD00001005270

• The_mutational_landscape_of_recurrent_Glioblastome_multiforme

  Targeted gene screen of approx 120 patients with primary GBM and recurrent samples.

  Study EGAS00001001764

• WGS_of_Somatic_Mosaicism_of_BRCA1_Methylation_in_Malignant_and_Nonmalignant_Breast_Tissue

  WGS of Somatic Mosaicism of BRCA1 Methylation in Malignant and Nonmalignant Breast Tissue

  Study EGAS00001008235

• EMseq_of_Somatic_Mosaicism_of_BRCA1_Methylation_in_Malignant_and_Nonmalignant_Breast_Tissue

  EMseq of Somatic Mosaicism of BRCA1 Methylation in Malignant and Nonmalignant Breast Tissue

  Study EGAS00001008236

• scRNAseq data of HGSOC patients before and after treatment

  scRNAseq data of HGSOC patients before and after treatment

  Dataset EGAD50000000191

• Whole exome sequencing of bulk primary tumor (and one lymph node metastasis) and matched blood of six non-metastatic breast cancer patients

  Dataset EGAD00001002746

• RNA-Seq and WXS from 6 glioblastoma patients

  RNA-Seq and WXS from 6 glioblastoma patients

  Dataset EGAD00001003293

• IfGH-10772

  Clinical and genetic information of an individual with RVOT-VT and a KCNK2 (TREK1) gene mutation obtained after whole exome sequencing.

  Dataset EGAD00001003328

• H3Africa NEEDI SNPs and INDELs

  SNPs and INDELs of novel hereditary neurological disease genes in Mali using Beckman 8800, ABI 3730/3730xl.

  Dataset EGAD00001006295