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• NeurOmics_HD_Biomarker-1_V1

  This data set includes RNAseq data from 136 samples from the TRACK-HD cohort including premanifest, manifest and control subjects. Data can only be used for Huntington's disease related research.

  Dataset EGAD00001002699

• Somatic genetic basis of Wilms' tumour

  We investigated the somatic genetic basis of Wilms' tumour and found complex phylogenetic relations between tumours

  Dataset EGAD00001005136

• Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing

  The dataset comprises of muscle samples from three patients with mitochondrial disease: Patient 1, age9; Patient 2, age16; and Patient 3, age 58.

  Dataset EGAD00001006079

• RNA-Seq data of de novo assembly individual EGYPT

  This is the blood RNA-Seq read data used for expression analysis such as haplotypic expression (mapped against GRCh38).

  Dataset EGAD00001006036

• NICHE - RNA-seq of MMR proficient and MMR deficient early stage colon cancers

  The dataset includes 77 FASTQ files from single-end total RNA sequencing on Illumina HiSeq2500 for 39 patients.

  Dataset EGAD00001006042

• Alveolar Rhabdomyosarcoma sequencing data

  This dataset comprises DNA sequencing for tumor and matched normal from an Alveolar Rhabdomyosarcoma patient. It also include RNA sequencing data from the tumor sample.

  Dataset EGAD00001006622

• WES of CTCL patients

  Paired end whole exome sequencing (WES) data of tumor/normal pairs (sorted malignant CD3+/Vb+ T-cells and CD19+ non-malignant B-cells) for the identification of somatic mutation.

  Dataset EGAD00001006895

• GCAT| WGS VCF QC Genotype V1

  This dataset contains genotypes (35.4M of SNVs, Indels and SVs), from 785 samples, after QC filtering, from the 808 WGS GCAT cohort.

  Dataset EGAD00001007774

• 666PG Somatic CNA calls

  Filtered somatic CNA calls detected using Battenberg from the CPCGGene 666PG study

  Dataset EGAD00001007699

• Sequencing data for the manuscript "Multi-focal sampling of de novo metastatic prostate cancer reveals complex polyclonality and enables accurate clinical genotyping"

  This submission includes targeted and whole exome paired-end fastq files.

  Dataset EGAD00001009651