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• Whole genome sequencing dataset from: Biased allelic expression in human primary fibroblast single cells.

  Dataset EGAD00001001083

• Germline snv g.vcf for EGAS00001004572

  Bulk Germline snv vcfs from haplotypecaller analysis in EGAS00001004572

  Dataset EGAD00001006910

• Genetics of gene expression in primary human immune cells Data Access Committee

  Dac EGAC01000000009

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

  Metagenomic sequencing of human fecal samples

  Dataset EGAD50000000258

• CNS and systemic relapse in DLBCL

  Microarray data for 230 DLBCL patients

  Dataset EGAD00010001909

• Transcriptome dataset from: Biased allelic expression in human primary fibroblast single cells.

  Dataset EGAD00001001084

• Deep sequencing of 151 cancer genes

  Deep sequencing of 151 cancer genes in 6 synchronous CRC of 3 patients

  Dataset EGAD00001001870

• Heterogeneous Genomic Evolution and Immune Microenvironments in Metastatic Lung Cancer

  WES data of paired primary and metastatic tumors

  Dataset EGAD00001006213

• A non-canonical lymphoblast in refractory childhood T-cell leukaemia

  This dataset contains 75 WGS samples of T-ALL (including matched remission samples where available).

  Dataset EGAD00001015727

• EHMT2 alterations cause a Kleefstra-like syndrome

  We report clinical and molecular correlates associated with six de novo EHMT2 variants identified in patients presenting with a Kleefstra syndrome–like phenotype. Transcriptomic profiling of patient-derived fibroblasts and induced pluripotent stem cells (iPSCs) reveals shared gene expression signatures between EHMT2 variant carriers and Kleefstra syndrome, compared with cell lines derived from healthy donors.

  Study EGAS50000001637