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• WES files for Newman MAP3K8 melanoma

  WES files for Newman MAP3K8 melanoma paper titled "Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas"

  Dataset EGAD00001004566

• WGS files for Newman MAP3K8 melanoma

  WGS files for Newman MAP3K8 melanoma paper titled "Clinical genome sequencing uncovers potentially targetable truncations and fusions of MAP3K8 in spitzoid and other melanomas"

  Dataset EGAD00001004579

• Dataset for "Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability"

  Dataset for "Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability"

  Dataset EGAD00001000691

• Thymic epithelial transplantation for complete DiGeorge syndrome: RNA (2025-10-02)

  Single cell transcriptomics study of thymic transplant biopsies . This dataset contains all the data available for this study on 2025-10-02.

  Dataset EGAD00001015721

• Tumour sample for patient SA1026

  Whole genome sequencing of tumour sample for triple negative breast cancer patient SA1026

  Dataset EGAD00001009607

• DATA FILES FOR MULLIGHAN MEF2D RNASEQ UNSTRANDED

  DATA FILES FOR MULLIGHAN MEF2D RNASEQ UNSTRANDED

  Dataset EGAD00001002704

• Illumina Reads for patient with ataxia-pancytopenia syndrome.

  Illumina BAMs for a patient with ataxia-pancytopenia syndrome and both of their parents.

  Dataset EGAD00001005034

• Whole Genome Sequencing data for epigenetic subgroups of meningioma

  Bam files for 124 samples (62 tumor vs blood pairs); Whole Genome Sequencing performed on Illumina HiSeq X Ten

  Dataset EGAD00001005061

• ChIP-seq for AR, FOXA1 and HOXB13 on 8 prostectomy samples

  ChIP-seq for AR, FOXA1 and HOXB13 on 8 prostectomy samples, both regions with/-out tumor cells, Fastq files.

  Dataset EGAD00001005374

• SCRNA10X_SA_CHIP0141_004

  Transcriptome profiling by high-throughput sequencing for single cells for library SCRNA10X_SA_CHIP0141_004 1 samples; filetype=fastq

  Dataset EGAD00001006463

• TENX068

  Transcriptome profiling by high-throughput sequencing for single cells for library TENX068 1 samples; filetype=fastq

  Dataset EGAD00001006482

• TENX069

  Transcriptome profiling by high-throughput sequencing for single cells for library TENX069 1 samples; filetype=fastq

  Dataset EGAD00001006483

• IMpower133 processed RNA-seq data whole transcriptome

  This dataset contains log2(TPM + 1) for 271 tumor samples profiled by RNA-seq for the entire transcriptome.

  Dataset EGAD00001006927

• Normal sample for patient SA533

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA533

  Dataset EGAD00001009571

• Normal sample for patient SA597

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA597

  Dataset EGAD00001009572

• Normal sample for patient SA997

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA997

  Dataset EGAD00001009573

• Normal sample for patient SA1027

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA1027

  Dataset EGAD00001009588

• Normal sample for patient SA1028

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA1028

  Dataset EGAD00001009589

• Normal sample for patient SA1040

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA1040

  Dataset EGAD00001009590

• Normal sample for patient SA1058

  Whole genome sequencing of normal sample for triple negative breast cancer patient SA1058

  Dataset EGAD00001009672

• single cell RNA sequencing for healthy controls and patients having NFATc1 deficiency

  single cell RNA sequencing for 4 healthy controls and 2 patients having NFATc1 deficiency

  Dataset EGAD00001011044

• Genotype-Tissue Expression (GTEx) (2025-07-28)

  Dual snRNAseq and ATACseq of replicate PBMC samples for 10X beta testing. . This dataset contains all the data available for this study on 2025-07-28.

  Dataset EGAD00001015663

• WTCCC case-control study for Coronary Artery Disease - Combined Controls

  WTCCC genome-wide case-control association study for Coronary Artery Disease (CAD) using six disease collections together with the 1958 British Birth Cohort and the UK National Blood Service collections as controls.

  Study EGAS00000000004

• WTCCC case-control study for Type 1 Diabetes - Combined Controls

  WTCCC genome-wide case-control association study for Type 1 Diabetes (T1D) using six disease collections together with the 1958 British Birth Cohort and the UK National Blood Service collections as controls.

  Study EGAS00000000015

• WTCCC case-control study for Type 2 Diabetes - Combined Controls

  WTCCC genome-wide case-control association study for Type 2 Diabetes (T2D) using six disease collections together with the 1958 British Birth Cohort and the UK National Blood Service collections as controls.

  Study EGAS00000000017