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Extracellular transcriptome in seminal plasma for non-invasive prostate cancer diagnosis
Study
EGAS00001005277
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Genomic landscape of inflammatory breast cancer by whole-genome sequencing
Study
EGAS00001004117
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INSIGHT: VHL Case Report
Study
EGAS00001005895
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Circulating tumor cell copy-number heterogeneity in ALK-rearranged non-small-cell lung cancer resistant to ALK inhibitors
Study
EGAS00001005301
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The genomic and radiomic complexity of multifocal prostate cancer
Study
EGAS00001002767
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An integrated molecular study of 20 hepatoblastoma pairs using whole genome sequencing and RNA sequencing
Study
EGAS00001002772
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Phylogenetic analysis of treatment-naive metastases using whole exome and genome sequencing data
Study
EGAS00001002777
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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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Real-time response profiling through serial plasma analyses during FOLFOX treatment in patients with colorectal cancer
Study
EGAS00001004213
-
MutWP4__CRUK_Grand_Challenge_Mutographs_of_Cancer__Gastric_Organoids
Study
EGAS00001003151
-
Ulcerative colitis study - WES data
Study
EGAS00001003801
-
Comprehensive molecular profiling of high-grade serous ovarian cancer
Study
EGAS00001003804
-
NanoSring of PBMC from bladder cancer and RCC patients
Study
EGAS00001004229
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MutWP1__CRUK_Grand_Challenge_Mutographs_of_Cancer__Oesophageal_adenocarcinoma
Study
EGAS00001003702
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
Single-cell RNA sequencing of chemotherapy-resistant muscle-invasive urothelial bladder cancer
Study
EGAS00001004233
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Integrated genomic analysis identifies driver genes and cisplatin-resistant progenitor phenotype in pediatric liver cancer
Study
EGAS00001005108
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Pediatric tumor in a single child of three large nuclear families
Study
EGAS00001005321
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Accurate detection and classification of pediatric sarcomas based on cell-free DNA fragmentation patterns
Study
EGAS00001005127
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Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
Study
EGAS00001005325
-
Mutational_landscape_in_haemochromatosis__exome_
Study
EGAS00001005158
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Clonal_dynamics_and_mutation_burden_in_male_germline___DupSeq
Study
EGAS00001005135
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A novel breast cancer cell line derived from a metastatic bone lesion of a breast cancer patient
Study
EGAS00001002840
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Epigenomic profile of diverse cancer
Study
EGAS00001004352
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Genomic and functional fidelity of small cell lung cancer patient-derived xenografts
Study
EGAS00001002853
-
Colorectal adenomas, carcinomas and adjacent normal NKI-AvL TGO series NGS-ProToCol
Study
EGAS00001002854
-
Evolution_of_the_cancer_epigenome_in_myeloproliferative_neoplasms_TGS
Study
EGAS00001003863
-
Small_molecule_inhibitors_in_melanoma___Kenski___Kong___WES
Study
EGAS00001002863
-
Exploring_the_heterogeneity_of_sarcoma_using_single_cell_sequencing_
Study
EGAS00001002866
-
Whole genome analysis of mutation hotspots in gastric cancer
Study
EGAS00001002872
-
Foundation Medicine Genomic Data Used to Identify Prognostic Markers and Fusion Genes in Multiple Myeloma
Study
EGAS00001002874
-
Phylogenetic reconstruction of breast cancer
Study
EGAS00001004356
-
RNA-seq of Liver Cancer
Study
EGAS00001002879
-
Genomic DNA of tumor tissues, adjacent normal tissues, and peripheral blood were extracted using QIAamp DNA mini Kit (QIAGEN, cat. #51306)
Study
EGAS00001003242
-
Integrated clinical, whole genome, and transcriptome analysis of multisampled lethal metastatic prostate cancer
Study
EGAS00001001659
-
Cell-free DNA analysis reveals POLR1D-mediated resistance to bevacizumab in colorectal cancer
Study
EGAS00001003791
-
A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
-
Whole Genome Sequencing of HCC
Study
EGAS00001002888
-
Somatic_mutation_profiling_of_intestinal_crypts_from_IBD
Study
EGAS00001002896
-
2015_AML_ETO
Study
EGAS00001002897
-
2015_AML_ETO_WGS_additional
Study
EGAS00001002898
-
SCLC tumor sequencing
Study
EGAS00001003985
-
Accurate mapping of mitochondrial DNA deletions and duplications using deep sequencing
Study
EGAS00001004380
-
Whole_Genome_sequencing_of_rhabdomyosarcoma_tumour_tissue
Study
EGAS00001008274
-
Circulating tumor cells Exome sequencing from breast cancer
Study
EGAS00001005228
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Matching of actionable mutations with therapies in cancer patients: comparison of three commercial decision support platforms
Study
EGAS00001004383
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Combining a Universal Telomerase Based Cancer Vaccine with Ipilimumab in Patients with Metastatic Melanoma - Five-year Follow up of a Phase I/IIa Trial
Study
EGAS00001005253
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Scottish High Grade Serous Ovarian Cancer
Study
EGAS00001004410
-
PELICAN33 longitudinal clinical and autopsy phenomic assessment in lethal metastatic prostate cancer
Study
EGAS00001005399
-
Preservation of stemness in high-grade serous ovarian cancer organoids requires low Wnt environment
Study
EGAS00001003821