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• Complex structural variation patterns in pediatric solid tumors WGS

  Paired tumor-normal whole genome sequencing data from primary tumors of patients diagnosed with neuroblastoma, Ewing sarcoma, Wilms tumor, hepatoblastoma and rhabdomyosarcoma

  Dataset EGAD00001011378

• Dataset RNAseq from regions of insitu and invasive human mammary ductal disease

  BAM files from RNAseq study from regions of insitu and invasive human mammary ductal disease

  Dataset EGAD00001008586

• 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

• scRNAseq of ARID1B+/+ (control) and ARID1B+/- human telencephalic organoids at D120

  This dataset contains scRNAseq data of human telencephalic organoids, at day 120, from 4 different sequencing runs (libraries), as follows (please see cell line clone nomenclature in original publication): 1. Library 177136: Pat.2 ARID1B+/+ clone 2c (2 organoids, E11rep_1, E11rep_2), Pat.2 ARID1B+/- clone 2a (2 organoids: B002orig_1, B002orig_2) 2. Library 178119: Pat.2 ARID1B+/+ clone 2c (3 organoids: E11rep_1, E11rep_2, E11rep_3), Pat.2 ARID1B+/- clone 2a (3 organoids: B002orig_1, B002orig_2, B002orig_3) 3. Library 178120: Pat.2 ARID1B+/+ clone 2d (3 organoids: A3rep_1, A3rep_2, A3rep_3), Pat.2 ARID1B+/- clone 2b (3 organoids: B002_F7_1, B002_F7_2, B002_F7_3) 4. Library 184337: Pat.1 ARID1B+/- clone 1a (3 organoids: B001orig_1, B001orig_2, B001orig_3), HD.1 ARID1B+/+ clone 3a (3 organoids: 176_1, 176_2, 176_3), HD.1 ARID1B+/- clone 3b (3 organoids: F10_1, F10_2, F10_3)

  Dataset EGAD50000000498

• prcmd-G-1

  Genetic studies of pregnancy-related cardiometabolic disorders in Central Asian, Northern European, and Colombian populations

  Dataset EGAD00010001212

• Chondrosarcoma Targeted Sequencing Study

  This Study uses a focused bespoke bait pull down library method to target findings of Chondrosarcoma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Dataset EGAD00001000265

• Osteosarcoma Targeted Sequencing Study

  This Study uses a focused bespoke bait pull down library method to target findings of Osteosarcoma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Dataset EGAD00001000266

• Chordoma Targeted Sequencing Study

  This Study uses a focused bespoke bait pull down library method to target findings of Chordoma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Dataset EGAD00001000267

• Meningioma Targeted Sequencing Study

  This Study uses a focused bespoke bait pull down library method to target findings of Meningioma whole genome and whole exome sequencing studies in order to validate findings. This method will also be used on a larger set of tumour only samples in order to find precedence of these findings in a larger set of patient samples.

  Dataset EGAD00001000273

• Whole genome sequencing data of high-grade serous ovarian cancer samples (set 6)

  Whole genome sequencing data of 31 high-grade serous carcinoma (HGSC) patients (101 samples) sequenced with HiSeq X Ten and BGISEQ-500

  Dataset EGAD00001010202

• WES data

  WES FASTq files of 76 bulk pre-treatment tumors and 76 matched peripheral blood mononuclear cells from GO30140 group A

  Dataset EGAD00001008129

• 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

• 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

• 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

• 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

• 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

• TRACERx NSCLC - Whole exome multiregion sequencing data from the 421 cohort

  TRACERx NSCLC - Whole exome multiregion sequencing data from the 421 cohort

  Dataset EGAD00001009825

• LBC1936 fastq files

  1075 members of the LBC1936 were sequenced using the Illumina HiSeq X platform. This dataset contains the paired fastq files.

  Dataset EGAD00001008774

• Covid19 Gene expression

  The dataset contains the gene expression profile of each individual along with gene fusion events.

  Dataset EGAD00001010185

• WGS of OvCa

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

  Dataset EGAD00001008581

• UK10K_COHORT_ALSPAC REL-2012-06-02

  UK10K_COHORT_ALSPAC REL-2012-06-02: Low-coverage whole genome sequencing; variant calling, genotype calling and phasing

  Dataset EGAD00001000740

• UK10K_COHORT_TWINSUK REL-2012-06-02

  UK10K_COHORT_TWINSUK REL-2012-06-02: Low-coverage whole genome sequencing; variant calling, genotype calling and phasing

  Dataset EGAD00001000741

• Whole genome landscape of adult T-cell leukemia/lymphoma

  Whole-genome sequence (WGS) data of tumor-normal pairs from 139 ATL patients and RNA sequence (RNA-seq) data of tumors from 28 ATL patients.

  Dataset EGAD00001008289

• Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer

  Dataset EGAD00001007858

• Dual targeting of polyamine synthesis and uptake in diffuse intrinsic pontine gliomas

  Bulk RNA-seq data of tumour data.

  Dataset EGAD00001006794

• EPICC: Evolutionary Predictions in Colorectal Cancer

  ATAC-seq profiling bam files from colorectal carcinoma and adenoma.

  Dataset EGAD00001008140

• Next Generation Children project

  Whole genome sequencing of sick children in neonatal and paediatric intensive care units, aligned to reference assembly GRCh38.

  Dataset EGAD00001007868

• EPICC: Evolutionary Predictions in Colorectal Cancer WGS-3

  WGS profiling bam files from colorectal carcinoma and adenoma.

  Dataset EGAD00001008642

• WGS samples for study EGAS00001001623

  Dataset EGAD00001001856