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Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
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Same-day genomic and epigenomic diagnosis of brain tumors using realtime nanopore sequencing
Study
EGAS00001002213
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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
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WES_of_adult_intellectual_disabilities_with_co_morbid_psychiatric_disorders
Study
EGAS00001002962
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Short and long-read genome sequencing methodologies for somatic variant detection; genomic analysis of a patient with diffuse large B-cell lymphoma
Study
EGAS00001004266
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Reduced Representation Bisulfite Sequencing (RRBS) in various tissues to discover DNA methylation markers for the diagnosis of breast and ovarian cancer.
Study
EGAS00001002609
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Multiple Myeloma Total Therapy trial patient sequencing
Study
EGAS00001003223
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High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Study
EGAS00001006103
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Immune induction strategies to enhance the sensitivity to PD-1 blockade in metastatic triple negative breast cancer: the TONIC-trial
Study
EGAS00001003535
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GDAP___Genome_Diversity_in_Africa_Project
Study
EGAS00001003602
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Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge
Study
EGAS00001006419
-
Repurposing azacitidine and carboplatin to prime immune checkpoint blockade-resistant melanoma for anti-PD-L1 re-challenge
Study
EGAS00001006420
-
ctDNA quantification in Ewing sarcoma patients
Study
EGAS00001006433
-
Single Cell Dissection of the Tumour Microenvironment Reveals Dynamic Interplay Shaping the Tumour Immunity Continuum in Ovarian Cancer
Study
EGAS00001004935
-
Somatic copy number alteration and fragmentation analysis in circulating tumor DNA for cancer screening and treatment monitoring in colorectal cancer patients
Study
EGAS00001006490
-
The University of Hong Kong Colon Cancer GCV Study
Study
EGAS00001006707
-
High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform, P49-P104 and run1 replicates
Study
EGAS00001006595
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ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy
Study
EGAS00001006883
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One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Study
EGAS00001006886
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Separation of chronic myeloid leukemia stem cells from normal hematopoietic stem cells at single-cell resolution
Study
EGAS00001006904
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Molecular characterization of Barrett’s esophagus at single cell resolution
Study
EGAS00001005221
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Genome-wide DNA methylation sequencing identifies epigenetic perturbations in the upper airways under long-term exposure to moderate levels of ambient air pollution
Study
EGAS00001007374
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Substantial somatic genomic variation and selection for BCOR mutations in human induced pluripotent stem cells
Dataset
EGAD00001007029
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Dataset for Sarcoma RNA sequencing linked from study EGAS00001004813
Dataset
EGAD00001010276
-
RNAseq dataset for MALT1 in MCL
Dataset
EGAD00001009771
-
Solve-RD_RND_cohort-1_DF1+2_V1
Dataset
EGAD00001009769
-
A circulating biomarker for severity of facioscapulohumeral muscular dystrophy
Study
EGAS00001007350
-
Nala GSI GSAv3 PGx Study
Study
EGAS00001007710
-
NEOPREDICT-Lung: Neoadjuvant Immunotherapy for Resectable NSCLC
Study
EGAS00001007753
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The G2 gene expression signature and MYC overexpression are independent poor prognostic factors in childhood high-grade osteosarcoma
Study
EGAS00001008073
-
Whole exome and RNA sequencing of organoid samples derived from TRACERx patients
Study
EGAS00001008092
-
Raw bulk TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008118
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Molecular features of adenomas predicting metachronous colorectal cancer: a nested-case control study
Study
EGAS00001007039
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Whole genome and whole exome sequencing of serial biopsies of relapsed/refractory diffuse large B-cell lymphoma.
Study
EGAS00001007053
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Proteomic Analysis of Non-Muscle Invasive and Muscle Invasive Bladder Cancer Highlights Distinct Subgroups With Metabolic, Matrisomal, and Immune Hallmarks
Study
EGAS00001007290
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Single cell TCRseq data fromTIL and non-TIL expanded TRACERx samples in the manuscript Bulk TCRseq from TRACERx samples from 'Subclonal immune evasion in non-small cell lung cancer'
Study
EGAS00001008161
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Procardis study on novel susceptibility genes for coronary artery disease (CAD)
Study
EGAS00000000055
-
Wellcome Trust Sanger Institute
Dac
EGAC00001000205
-
Knoll et al.: The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Study
EGAS00001007461
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Neoadjuvant atezolizumab plus chemotherapy in gastric and gastroesophageal junction adenocarcinoma: the phase 2 PANDA trial
Study
EGAS50000000168
-
B cell receptor silencing reveals origin and dependencies of high-grade B cell lymphomas with MYC and BCL2 rearrangements
Study
EGAS50000001047
-
Expanding the SPTBN1 Spectrum: A Case of Neurodevelopmental Disorder with GI and Musculoskeletal Involvement
Study
EGAS50000001213
-
German early-onset prostate cancer cohort of the Pan-Prostate Cancer Genome (PPCG) project
Study
EGAS00001003373
-
Ancient Yakuts genomes and metagenomes
Dataset
EGAD50000001903
-
Automated machine-learning approach for next generation profiling of sequence alterations, mutation burden, microsatellite instability, and structural variants in human cancers
Study
EGAS00001005556