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• chr19_allsamples_imputated

  Chromosome 19 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002524

• chrX_allsamples_imputated

  Chromosome X imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002522

• chr3_allsamples_imputated

  Chromosome 3 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002521

• chr18_allsamples_imputated

  Chromosome 18 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002520

• chr8_allsamples_imputated

  Chromosome 8 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002519

• chr22_allsamples_imputated

  Chromosome 22 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002518

• chr9_allsamples_imputated

  Chromosome 9 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002535

• chr12_allsamples_imputated

  Chromosome 12 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002517

• chr2_allsamples_imputated

  Chromosome 2 imputed genotypes of samples genotyped on the Axiom Human Genotyping SARS-CoV-2 array (GRCh38)

  Dataset EGAD00010002523

• EGAD00010000288

  All cases and Finnish, Dutch, Italian control samples (Hap550)

  Dataset EGAD00010000288

• EGAD00010000286

  All cases and controls (Hap550)

  Dataset EGAD00010000286

• EGAD00010000292

  All cases and Finnish, Dutch, Italian control samples (Hap300)

  Dataset EGAD00010000292

• EGAD00010000298

  All cases and controls (Hap300)

  Dataset EGAD00010000298

• Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires forlibrary A96176A

  Transposase-based amplification-free single-cell genome direct library preparation in nanowell chips; 531 samples; filetype=bam

  Dataset EGAD00001004769

• GRP sWGS plasma DNA

  The dataset consists of shallow whole genome sequencing from plasma DNA of 1002 individuals, including 1048 samples. Raw fastq files from Illumina HiSeq series are available.

  Dataset EGAD00001008627

• Genome sequence data from a metastatic rectal carcinoma patient

  Genome sequence data from a metastatic rectal carcinoma patient, generated as part of the BC Cancer Agency's Personalized OncoGenomics (POG) study

  Dataset EGAD00001010972

• Genome sequence data from a metastatic paraganglioma patient

  Genome sequence data from a metastatic paraganglioma patient, generated as part of the BC Cancer Agency's Personalized OncoGenomics (POG) study

  Dataset EGAD00001010985

• Transcriptome sequence data from a metastatic breast cancer patient

  Transcriptome sequence data from a metastatic breast cancer patient, generated as part of the BC Cancer Agency's Personalized OncoGenomics (POG) study

  Dataset EGAD00001003690

• EGAD00010000246

  Coeliac disease cases and control samples. (1958BC samples excluded)

  Dataset EGAD00010000246

• Next Generation Children project

  Whole genome sequencing of sick children in neonatal and paediatric intensive care units, aligned to reference assembly GRCh37.

  Dataset EGAD00001007780

• A body map of somatic mutagenesis in morphologically normal human tissues

  This dataset contained raw sequencing fastq data of the article "A body map of somatic mutagenesis in morphologically normal human tissues". We sampled morphologically normal tissue biopsies from 5 donors. We performed low-depth WGS on 1,764 samples, high-depth WGS on 48 samples and WES on 1,772 samples.

  Dataset EGAD00001007859

• Solve-RD_ITHACA_cohort-1_DF1+2_V1

  Solve-RD data submitted to the ERN-ITHACA cohort for re-analysis (Data freeze 1+2) v1

  Dataset EGAD00001009770

• Mutation analysis of core biopsies from localized breast cancer patients

  Targeted next-generation sequencing (NGS) of 93 frequently mutated genes in breast cancer using the QIAseq Human Breast Cancer Targeted Panel (QIAGEN), which uses digital sequencing by incorporating unique molecular barcodes (UMI).

  Dataset EGAD00001008396

• WGS of OvCa

  WGS data relative to 63 primary and treatment-naive ovarian carcinomas, from independent donors.

  Dataset EGAD00001008581

• Irish Covid19 WGS Raw Reads

  Dataset contains 483 Irish origin Individuals with Covid19. paired end sequencing has been performed For WGS and later processed by using sention v 201808.03.

  Dataset EGAD00001010186