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Endometrial Cancer Association Consortium - OncoArray Genotypes
Study
phs001885
-
Context-specific regulatory genetic variation in MTOR dampens neutrophil-T cell crosstalk in pneumonia-associated sepsis, modulating disease
Study
EGAS50000000894
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Mutational signature in colorectal cancer induced by genotoxic pks+ E. coli
Study
EGAS00001003934
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BLUEPRINT DNase accessibility of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000954
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BLUEPRINT RNA-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000953
-
BLUEPRINT ChIP-seq of Epigenetic programming during monocyte to macrophage differentiation and trained innate immunity
Study
EGAS00001000951
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Origins and functional consequence of somatic mitochondrial DNA mutations
Study
EGAS00001000968
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Targeted de novo phasing and long-range assembly by template mutagenesis
Dataset
EGAD00001008444
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CRISPR screening in human trophoblast stem cells reveals both shared and distinct aspects of human and mouse placental development
Study
JGAS000659
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Bulk-tissue paired-end RNA-sequencing of anterior cingulate cortex samples derived from Lewy body disease patients
Dataset
EGAD00001007698
-
Microsatellite unstable colorectal cancers
Study
EGAS00001003366
-
Metagenomic data of patients with bipolar disorder or schizoprhenia spectrum disorder
Dataset
EGAD50000001414
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CSER: Exome Sequencing in Diverse Populations in Colorado and Oregon/CHARM Cancer Health Assessments Reaching Many
Study
phs002111
-
Temporal Evolution Reveals Bifurcated Lineages in Aggressive Neuroendocrine Small Cell Prostate Cancer Trans-Differentiation
Study
phs003230
-
Genome analysis of common diseases among older Japanese adults and development of clinical genome information storage
Study
JGAS000755
-
Discover Cancer Image Europe, the first release of the EUCAIM platform to fuel cancer research and data sharing
Blog
discover-cancer-image-europe
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A Scalable, GMP-Compatible, Autologous Organotypic Cell Therapy for Dystrophic Epidermolysis Bullosa
Study
phs003271
-
Metadata Submission
Documentation
submission/metadata/submission
-
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Gene Discovery in Autosomal Dominant Focal Segmental Glomerulosclerosis (FSGS)
Study
phs000777
-
Programmatic submission based on XML
Documentation
submission/metadata/submission/programmatic-submission-xml
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NSIGHT BabySeq Project
Study
phs002093
-
A study of the genetic basis of evation by Acute Myeloid Leukaemia of Graft vs Leukaemia effects after allogeneic bone marrow transplantation
Dataset
EGAD00001000404
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Molecular Tumor Board to Inform on Personalized Medicine for a Man with Advanced Prostate Cancer
Study
EGAS00001004648
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Deterministic Evolution and Stringent Selection During Pre-Neoplasia
Study
phs003249
-
RNA-seq
Dataset
EGAD50000002023
-
Transcriptional profiling of ovarian tumours and cell lines
Study
EGAS00001004814
-
Genomic characterization of NUT midline carcinoma
Study
EGAS00001001934
-
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Study
EGAS00001000599
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Genetic Basis of Early Onset Bicuspid Aortic Valve Disease
Study
phs003705
-
How upcycled prostate cancer sequences enabled key findings on telomeres length
Blog
prostate-cancer-sequences-enabled-key-findings-on-telomeres-length
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Mutational signatures in head and neck cancer (H019)
Study
EGAS00001004588
-
HiDEF-seq Single-Molecule Sequencing of Single-Strand Mismatches and Damage
Study
phs003604
-
Clonal dominance defines metastatic dissemination in pancreatic cancer
Study
EGAS00001006358
-
Parallel CRISPR Editing of Familial ALS Mutations
Study
phs002440
-
Whole genome sequencing data from tumor and normal samples
Dataset
EGAD50000001909
-
National Human Genome Research Institute (NHGRI) Clinical Sequencing Exploratory Research (CSER) The MedSeq Project: Integration of Whole Genome Sequencing into Clinical Medicine (HG006500)
Study
phs000958
-
Public Access Defibrillation Community Trial (PAD)(PAD-BioLINCC)
Study
phs003858
-
Maintenance of Brain Tumor Profile on Organotypic Brain Slice Culture (OBSC)
Study
phs003268
-
Download Metadata
Documentation
access/download/metadata
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Deep single-cell RNA sequencing data for 11138 T cells from tumour, adjacent normal tissue and peripheral blood of treatment-naive CRC patients. The DATA ACCESS AGREEMENT is provided at https://github.com/zhangyybio/single-T-cell-data-access. Applicants can request access to the data by directly downloading it or by sending an email to cancerpku@pku.edu.cn. The process that is used to approve an application includes verifying the institution, participants and research purposes of the application. In general this process will take about two weeks. In principal, any scientific research program complying with the laws and bioethic regulation policies of China will be approved.
Study
EGAS00001002791
-
Probabilistic cell type assignment of single-cell transcriptomic data reveals spatiotemporal microenvironment dynamics in human cancers
Study
EGAS00001003452
-
APOBEC3 mutagenesis drives therapy resistance in breast cancer
Study
EGAS50000000875
-
Structural Expression of BMMF in tissues of colorectal, lung and pancreatic cancer patients
Study
EGAS00001006744
-
Resource for Genetic Epidemiology Research on Adult Health and Aging (GERA)
Study
phs000674
-
CIDR: The Role of Rare Coding Variation in Prostate Cancer in Men of African Ancestry - RESPOND Project 2
Study
phs002637
-
Resuscitation Outcomes Consortium (ROC) Cardiac Epidemiologic Registry (Cardiac Epistry) Versions 1 and 2 (ROC-Cardiac Epistry 1 and 2-BioLINCC)
Study
phs003803
-
Timing and trajectory of BCR-ABL1 driven chronic myeloid leukaemia
Dataset
EGAD00001015473
-
The Primary Open-Angle Glaucoma Genes and Environment (GLAUGEN) Study
Study
phs000308
-
Innate myeloid cell sbuset-specific gene expression patterns in the human colon are altered in Crohn's disease patients
Study
JGAS000127
-
Microsatellite data show recent demographic expansions in sedentary but not in nomadic human populations in Africa and Eurasia.
Study
EGAS00001000652