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• WGS Sequencing of Urothelial Carcinoma from Taiwan

  Normal and Tumor paired WGS sequencing of UC Tissues

  Dataset EGAD50000001547

• WES of HNSCC PDX models

  Whole exome sequencing of cetuximab-sensitive and -resistant patient-derived xenograft models from two HNSCC patients.

  Dataset EGAD50000001176

• Targeted nanopore sequencing of FGF14 repeat expansions

  This dataset includes FASTQ files from FGF14 alleles sequenced by targeted nanopore in 67 patients, 64 control individuals and three unaffected relatives.

  Dataset EGAD50000000692

• Breast Invasive Lobular Carcinoma CDH1 WGS dataset

  We subjected to whole genome sequencing (WGS) one ILC case lacking CDH1 biallelic mutations. Both tumor and normal samples were sequenced.

  Dataset EGAD50000000696

• Normalised mRNA expressions

  Quantile-normalised and batch corrected

  Dataset EGAD00010001561

• APCDR AGV Baganda

  APCDR AGV Project: Array data from 100 Baganda. Raw data, intensity files and post-QC Plink files.

  Dataset EGAD00010001055

• WES dataset of mesothelioma CONFIRM study

  This dataset comprises 33 whole-exome sequencing (WES) samples from mesothelioma patients, including 18 tumor, 13 matched normal, and 2 relapsed samples.

  Dataset EGAD50000002621

• HGSOC-celllines-SmartSeq3

  Smart-seq3 scRNA-seq of cells from primary (OV2295) and metastatic (OV2295R2) high-grade serous ovarian cancer cell-line

  Dataset EGAD00001009798

• WGS from 68 MM patients

  Mutations calls from 68 MM patients collected with Mutect2. All tumor samples were CD138+ cells at diagnosis and all control samples were PBMCs.

  Dataset EGAD00001009692

• Colorectal Microenvironment Spatial Mapping Dataset

  Two samples derived from a colorectal cancer female patient - tumor tissue and normal adjacent tissue analyzed via Visium Spatial Gene Expression.

  Dataset EGAD00001015675

• Genomic heterogeneity recapitulated in a PDXovo model - WXS mapped reads

  Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance - WXS mapped reads

  Dataset EGAD00001003589

• Genomic heterogeneity recapitulated in a PDXovo model - WXS unaligned reads

  Ultra-Fast Patient-Derived Xenografts Identify Functional and Spatial Tumour Heterogeneities that Drive Therapeutic Resistance - WXS unaligned reads

  Dataset EGAD00001003590

• Whole-exome sequencing data of Hepato-Cholangiocarcinoma

  Hepatocellular carcinoma specimens, intrahepatic cholangiocarcinoma specimens and liver normal tissues collected from 7 samples, including 44 fastq files from whole exome sequencing.

  Dataset EGAD00001003892

• Integrated Genomic, Epigenetic, and Expression Analyses of Ovarian Cancer Cell Lines

  In this dataset there are 55 whole genome sequencing samples of epithelial ovarian carcinoma (bam files).

  Dataset EGAD00001004532

• Gene expression from human iPSC derived cortical neurons

  RNASeq gene expression profiles from 3 icas9 human iPSC derived cortical neurons treated with and without doxycycline.

  Dataset EGAD00001006559

• Whole-exome and transcriptome in RMS

  Whole-exome sequencing in 16 RMS casesWhole-transcriptome sequencing in 8 RMS cases

  Dataset EGAD00001001105

• DNMT3A microcephalic primordial dwarfism RRBS data

  RRBS sequence data from one control and one patient with de novo DNMT3A mutations resulting in microcephalic primordial dwarfism.

  Dataset EGAD00001004472

• Chad genetic diversity reveals an African history marked by multiple Holocene Eurasian migrations

  Whole-genome sequencing data from Chad and Lebanon.

  Dataset EGAD00001002742

• aGCT_WGS

  Contains 46 aGCT tumor sample WGS BAMs from 33 patients and corresponding 33 germline reference WGS BAMs from those 33 patients

  Dataset EGAD00001005999

• PitNET normal-tumor exome sequencing samples

  PitNET white blood cell DNA - tumor DNA exome sequencing samples with Illumina exome sequencing. Fifteen patients and total of 30 exomes.

  Dataset EGAD00001006390

• HNSCC Whole Exome Sequencing

  Whole exome sequencing data of 28 matched normal-tumor-relapse patients from Lübeck and Munich (Germany).

  Dataset EGAD00001006919

• Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia

  Large structural variants are easily detected by Hi-C sequencing as strong, distant signals on a Hi-C contact map. Translocations are frequently evident in B-ALL and accurate identification of these translocations can guide clinical treatment options. Here were apply shallow Hi-C sequencing as an unbiased, cost-effective approach to identify translocations among B-ALL patients.

  Study EGAS00001005605

• FWO-project G.0687.12_X10-WGS

  Profiling subclonal architecture and phylogeny in tumors by whole-genome sequence data mining and single-cell genome sequencing

  Dataset EGAD00001001429

• Colorectal organoids and tumour tissue

  Whole genome sequencing of single cell derived organoids from normal colon tissue and colorectal cancer.

  Dataset EGAD00001001447

• Comprehansive analysis of somatic mutations and genetic variations with whole genome sequencing

  Indetification of stractural variations by using of long read whole genome sequencing data

  Study JGAS000516