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• Genomewide association studies in ankylosing spondylitis

  The aim of this study was to identify genes associated with ankylosing spondylitis susceptibility in British and Australian individuals of European descent.

  Study EGAS00000000104

• ATAC-seq in KMS11 vs TKO cells

  ATAC-seq to determine chromatin accessibility in t(4;14) Myeloma cell line KMS11 and KMS11 cells with knock-out of the translocated NSD2 allele.

  Study EGAS50000000076

• MicroC in KMS11 and TKO cells

  MicroC to show high resolution chromatin interactions in t(4;14) Myeloma cell line KMS11 and KMS11 cells with knock-out of translocated NSD2 allele (KMS11 TKO).

  Study EGAS50000000078

• RNA sequencing of OM-ALI cultures derived from control and AD individuals exposed to SARS-CoV-2

  RNA sequencing of air-liquid interface (ALI) cultures of olfactory mucosa (OM) cells derived from control (n=3) and AD (n=3) individuals exposed to SARS-CoV-2.

  Dataset EGAD50000000598

• Elucidation of the pathomechanism of inflammatory muscle diseases using multi-omics analysis

  This study aims to elucidate the pathomechanism of inflammatory muscle disease. We performed multi-omics analysis of muscle biopsy samples from the patients.

  Study JGAS000636

• Whole-genome-sequencing and Whole-exome-sequencing in Spastic paraplegia

  To identify the genetic cause and modifiers of Spastic paraplegia, we performed Whole-genome-sequencing and Whole-exome-sequencing of Spastic paraplegia patients.

  Study JGAS000494

• Fluctuating DNA methylation tracks cancer evolution at clinical scale

  Long-read Nanopore data of fCpGs from Gabbutt & Duran-Ferrer (2025) for developing the EVOFLUx method to study cancer evolution via DNA methylation fluctuations.

  Study EGAS50000001192

• Nanopore sequencing of FSHD, BAMS and healthy control fibroblast cell lines

  The goal was to resolve the complex genetic and epigenetic structures of D4Z4 alleles, a macrosatellite whose desilencing results in FSHD.

  Study EGAS50000001065

• Pediatric B-cell precursor acute lymphoblastic leukemia RNA sequencing

  This dataset included 33 childhood B-cell precursor acute lymphoblastic leukemia RNA sequencing samples. All samples were subjected to Illumina pair-end sequencing.

  Study EGAS50000000763

• miRNA

  The purpose is to perform miRNA analysis on FACS sorted target immune cell populations to uncover novel potential miRNA diagnostic markers biomarkers predictive of therapy response but also possibly identify perturbed signaling pathways or miRNA targets of intervention with the use of agomirs/antagomirs.

  Dataset EGAD50000002025