-
Single cell chromatin accessibility profiles from myelofibrosis patients
Dataset
EGAD50000000234
-
Sequencing data for oesophageal and related samples - BOs release 4 (RNA)
Dataset
EGAD00001004023
-
Finding structural variation from the patient-derived xenografts of pediatric T-cell leukemia at the single-cell level
Dataset
EGAD00001004499
-
Targeted sequencing of genes recurrently mutated in AML - part2
Dataset
EGAD00001000747
-
Sequencing data for oesophageal and related samples - Mourikis et al (WGS)
Dataset
EGAD00001004775
-
RNA-seq data from 121 tumor samples with muscle invasive bladder cancer.
Dataset
EGAD00001006238
-
RNA of peripheral blood for pancreatic cancer and chronic pancreatitis
Dataset
EGAD00001006915
-
Raw molecular data for "Subclonal immune evasion in non-small cell lung cancer"
Dataset
EGAD00001015537
-
Therapeutic Resistance to PI3K-alpha Inhibitors
Study
EGAS00001000991
-
RNAseq of whole blood in 359 idiopathic pulmonary arterial hypertension patients reveals biological heterogeneity
Dataset
EGAD00001007981
-
WTCCC case-control study for Breast cancer - Combined Controls
Study
EGAS00000000025
-
cfDNA dataset with expanded panel for cfDNA cohort
Dataset
EGAD50000000667
-
Fastq data for smRNA-Seq assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001401
-
NGS sequencing for genes from the patients of OU Genome Project
Study
JGAS000568
-
WTCCC case-control study for Tuberculosis
Study
EGAS00000000027
-
cfDNA dataset with whole genome sequencing for cfDNA cohort
Dataset
EGAD50000000666
-
WGS files for Klco PanAML data
Dataset
EGAD00001011295
-
RNASeq files for Klco PanAML data
Dataset
EGAD00001011294
-
WXS files for Klco PanAML data
Dataset
EGAD00001011296
-
Re-aligned BAM files for manuscript titled Discrepancies in Tumour Mutation Burden (TMB) reporting from sequential Endobronchial ultrasound trans bronchial needle aspiration (EBUS TBNA) samples within single lymph node stations for Copy Number Variant Calling.
Dataset
EGAD00001012638
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Cryopreservation of human cancers conserves tumour heterogeneity for single-cell multi-omics analysis
Dataset
EGAD00001007030
-
WTCCC case-control study for Ankylosing Spondylitis - Combined Controls
Study
EGAS00000000019
-
WTCCC case-control study for Autoimmune Thyroid Disease - Combined Controls
Study
EGAS00000000021
-
Whole Genome Sequencing Reveals Potential Therapeutic Strategy for Monomorphic Epitheliotropic Intestinal T-cell Lymphoma
Study
EGAS00001003876
-
Fastq data for whole genome shotgun sequencing for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001400
-
Fastq data for stranded mRNA-Seq assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001402
-
Fastq data for ChIP-Seq (H3K27ac) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001403
-
Fastq data for ChIP-Seq (H3K27me3) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001404
-
Fastq data for ChIP-Seq (H3K36me3) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001405
-
Fastq data for ChIP-Seq (H3K4me1) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001406
-
Fastq data for ChIP-Seq (H3K4me3) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001407
-
Development of a fully human glioblastoma-in-brain-spheroid model for accelerated translational research
Study
EGAS50000000757
-
Patient-Parent trio sequencing for 100 sporadic ID patients
Dataset
EGAD00001000680
-
DAC for Melanoma Exome Dataset for Identification of Mutated Epitopes
Dac
EGAC00001000546
-
Helmholtz Centre for Infection Research, Centre for Individualised Medicine
Dac
EGAC00001002208
-
Helmholtz Centre for Infection Research, Centre for Individualised Medicine
Dac
EGAC00001002844
-
Helmholtz Centre for Infection Research, Centre for Individualised Medicine
Dac
EGAC00001003086
-
Helmholtz Centre for Infection Research, Centre for Individualised Medicine
Dac
EGAC00001003058
-
NIHR BioResource Rare Diseases WGS project - Bleeding, Thrombotic and Platelet Disorders (BPD) Rare Disease domain
Dataset
EGAD00001004519
-
NIHR BioResource Rare Diseases WGS project - Neurological and Developmental Disorders (NDD) Rare Disease domain
Dataset
EGAD00001004522
-
Whole genome sequencing in prime-edited human organoids
Dataset
EGAD00001006352
-
Fecal WMS HV sequencing data
Dataset
EGAD00001008841
-
Single nuclei RNA-Seq from 5 regions of the human fetal brain
Dataset
EGAD00001009303
-
Organoid Derivation Project - GRCh38 - WGS (2023-06-22)
Dataset
EGAD00001011093
-
Helmholtz Centre for Infection Research, Centre for Individualised Medicine
Dac
EGAC00001002303
-
DAC for Sarcopenia HNSCC
Dac
EGAC50000000420
-
Center for Technology Licensing at Cornell University for data associated with Nature Medicine 2024 paper
Dac
EGAC50000000207
-
GoT2D WGS analysis files
Dataset
EGAD00010001185
-
Whole Exome Sequencing of healthy Spanish individuals
Study
EGAS00001000938