-
Sequence Analysis of Mutations and Translocations Across Breast Cancer Subtypes
Study
phs000369
-
Improved Detection and Identification of Microsatellite Instability Features in Colorectal Cancer
Study
phs001914
-
Biomarker Research for Anti EGFR Monoclonal Antibodies by Comprehensive Cancer Genomics
Study
JGAS000779
-
Insights into BRCA1 and TP53 associated breast cancer development from integrated whole genome analysis of mouse model mammary tumors
Study
EGAS50000001402
-
Long-read whole genome sequencing of gastric cancer
Study
EGAS50000001607
-
bulk RNAseq analysis of tumor from 3 non-muscle-invasive bladder cancer patients
Study
EGAS50000001383
-
HIPSD&R-seq enables scalable genomic copy number and transcriptome profiling
Study
EGAS50000000691
-
A Combined Omics and Tissue Biobank for Paediatric Cancers
Study
EGAS50000000209
-
Comprehensive Genomic Characterization of Acral Melanoma
Study
phs001036
-
GWA Study of Oral Cavity, Pharynx and Larynx Cancers in European, and North and South American Populations - CIDR
Study
phs002503
-
Spatial transcriptome analysis for elucidating progression of early lung adenocarcinoma
Study
JGAS000677
-
Whole-exome sequencing performed on a patient with chronic myelomonocytic leukemia and B cell acute lymphoblastic leukemia
Study
EGAS00001005117
-
Diverse modes of genomic alterations in hepatocellular carcinoma
Study
EGAS00001000824
-
Myelodysplastic_Syndrome_Exome_Sequnecing
Study
EGAS00001000089
-
Developing somatic copy number and mutation calling tools for a bespoke sequencing platform
Study
EGAS00001007195
-
Subclonal evolution of four ER+ breast cancers determined by WGS and scRNA-Seq
Study
EGAS00001002436
-
Identification of New Therapeutic Targets for Renal Medullary Carcinoma via Integrated Genomic and Transcriptomic Profiling
Study
EGAS50000001280
-
RNA-seq of CRC patient-derived xenograft tumors
Study
EGAS50000000598
-
Tumor-resident T-cell regulate responses to checkpoint blockade immunotherapies
Study
EGAS50000000826
-
Whole-exome sequencing of Fanconi anemia-like inherited bone marrow failure syndrome
Study
EGAS00001003809
-
Clinical efficacy and biomarker analysis of neoadjuvant atezolizumab in operable urothelial carcinoma in the ABACUS trial
Study
EGAS00001004445
-
GBM cancer stem cell lines -RNA-seq and WGS data
Study
EGAS00001003700
-
MSI_Cancer_Models___RNAseq
Study
EGAS00001004180
-
Epigenetic Intratumor Heterogeneity and Clonal Evolution in Aggressive Prostate Cancer
Study
EGAS00001000682
-
Orphan_Tumour_Study___RNAseq
Study
EGAS00001002534
-
CRISPR_screen_M14__NCI_H3122
Study
EGAS00001001060
-
Cell_lines_with_telomere_fusion_induced_rearrangements
Study
EGAS00001001059
-
Targeted_sequencing_of_embryonic_variants___Warm_Autopsy
Study
EGAS00001003952
-
Expressed_fusion_transcripts_in_rare_bone_tumours
Study
EGAS00001000763
-
Use_of_deep_sequencing_to_detect_clonal_mutations_in_sun_exposed_human_epidermis___whole_genome
Study
EGAS00001000860
-
Psoriatic_arthritis
Study
EGAS00001002104
-
IDH1 Somatic Mutation Profile in Intrahepatic Cholangiocarcinoma
Study
EGAS50000001638
-
Benchmarking_CRISPR_Whole_genome_Drop_out_Screen___B_S
Study
EGAS00001002931
-
FWO_project_G_0687_12_X10_WGS
Study
EGAS00001001145
-
AC-ICAM: An Atlas and Compass of Immune-CAncer-Microbiome Interactions in Colon Cancer
Study
phs002978
-
Somatic Mutation in Normal Bladder Study
Study
phs004105
-
HeLa Cell Genome Sequencing Studies
Study
phs000640
-
Whole genome and transcriptome analysis of a sporadic and recurring parathyroid carcinoma
Study
EGAS00001000484
-
Bladder cancer subtyping study across 4 atezo clinical trials
Study
EGAS50000000497
-
Oncogenic Ectodomain deletion of FGFR1 caused by Breakage-Fusion-Bridges in Squamous Cell lung Cancer
Study
EGAS00001005059
-
Whole genome sequencing of matched primary and metastatic acral melanomas
Study
EGAS00001000169
-
Localised colon cancer WES study contaning WBCs, tissue and plasma samples at different time points
Study
EGAS50000000204
-
Multimodal plasma and urinary cell-free DNA profiling improves risk stratification in newly diagnosed prostate cancer
Study
EGAS00001008195
-
Whole Exome Sequencing of Pancreatic Neuroendocrine Tumors at The Human Genome Sequencing Center, Baylor College of Medicine (HGSC-BCM)
Study
phs000871
-
International Cancer Proteogenomics Consortium (ICPC): Proteogenomics of East-Asian Breast Cancer
Study
phs003150
-
A Multi-Gene Mutation Classification of 468 Colorectal Cancers Reveals a Prognostic Role for APC
Study
phs001111
-
Genomic Analysis of Fibrolamellar Hepatocellular Carcinoma
Study
phs000828
-
Retinoblastoma Aqueous Humor Liquid Biopsy Repository
Study
phs003077
-
HiDEF-seq Single-Molecule Sequencing of Single-Strand Mismatches and Damage
Study
phs003604
-
Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
Study
EGAS00001003206
-
Genome-wide mutational consequences of nucleotide excision repair-deficiency through XPC deletion in a human adult stem cell culture
Study
EGAS00001002681
-
Long-read-transcriptome-sequencing of CLL and MDS patients uncovers common molecular effects of SF3B1 mutations
Study
EGAS50000000053
-
Prediction of plasma ctDNA fraction and prognostic implications of liquid biopsy in advanced prostate cancer
Study
EGAS50000000211
-
Primary prostate Hi-C
Study
EGAS00001005014
-
Automated image-based profiling of complex drug induced phenotypes in patient-derived organoids
Study
EGAS00001003140
-
Spatio-temporal analysis of prostate tumors in situ suggests pre-existence of treatment-resistant clones
Study
EGAS00001006113
-
Functional screening on patient-derived organoids identifies a therapeutic bispecific antibody that triggers EGFR degradation in LGR5+ tumor cells
Study
EGAS00001004584
-
The miR-185/PAK6 Axis Predicts Therapy Response and Regulates Survival of Drug-Resistant Leukemic Stem Cells in Chronic Myeloid Leukemia
Study
EGAS00001004153
-
Long-read sequencing of diagnosis and post-therapy medulloblastoma reveals complex rearrangement patterns and epigenetic signatures (Hipo_021)
Study
EGAS00001006629
-
Intratumoral Heterogeneity and Clonal Evolution Induced by HPV Integration.
Study
EGAS00001006652
-
Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification (H021)
Study
EGAS00001006706
-
Acral melanoma targeted exome sequencing study (UCSF)
Study
phs001596
-
Molecular Characterization of Large Cell Neuroendocrine Carcinoma of the Lung
by Multilayered Omics Analysis
Study
JGAS000832
-
Reproducibility of variant calls in replicate next generation sequencing experiments
Study
EGAS00001000826
-
cfDNA methylation profiling on longitudinally collected blood plasma of patients with esophageal adenocarcinoma
Study
EGAS50000000514
-
Transcriptomic insights into IPMN-associated PDAC progression
Study
EGAS50000001540
-
Germline WES of serrated polyposis syndrome
Study
EGAS50000000765
-
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments
Study
EGAS00001001822
-
Prospective high-throughput genome profiling in advanced cancers:
Study
EGAS00001004554
-
The Landscape of Genetic Alterations in Hepatocellular Carcinoma, 88 matched HCC tumour/normal pairs WGS belongs to ICGC LICA-CN project
Study
EGAS00001002218
-
DNA sequencing for human normal endometrial glands
Study
EGAS00001005822
-
Epigenetic analyses of methylation and nucleosome occupancy in cell-free DNA (cfNOMe)
Study
EGAS00001004370
-
Res1_PC9_exp2_MC_01_04_22
Study
EGAS00001006170
-
PREDICT
Study
EGAS00001000094
-
Myeloma_Follow_up_Pilot
Study
EGAS00001000743
-
Res1_PC9_exp1_MC_29_03_22
Study
EGAS00001006169
-
Randomized Phase II 2 x 2 Factorial Trial of the Addition of Carboplatin +/- Bevacizumab to Neoadjuvant Weekly Paclitaxel Followed by Dose-Dense AC in Hormone Receptor-Poor/HER2-Negative Resectable Breast Cancer
Study
phs001863
-
CIDR Estrogen Receptor Negative Breast Cancer in African American Women: DNA Methylation, Reproductive Events, and Mammary Epithelial Cell Populations
Study
phs002688
-
Impaired HLA Class I Antigen Processing and Presentation as a Mechanism of Acquired Resistance to Immune Checkpoint Inhibitors in Lung Cancer
Study
phs001464
-
Translating Gene-Calcium Interactions to Precision Medicine for Colorectal Cancer
Study
phs002164
-
Single cell transcriptomics to characterize the tumor microenvironment of prostate cancer fusion biopsies
Study
EGAS50000000888
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Clinical validity of post-surgery circulating tumor DNA (ctDNA) in stage III colon cancer patients treated with adjuvant chemotherapy: the PROVENC3 study
Study
EGAS50000000804
-
TGS___Comprehensive_Molecular_Characterization_of_Colorectal_Cancer_Metastases__MOSAIC_
Study
EGAS00001000958
-
Comparison of sequencing assays for sensitive detection of circulating tumour DNA in stage IA-IV breast cancer
Study
EGAS00001006040
-
Clonal dominance defines metastatic dissemination in pancreatic cancer
Study
EGAS00001006358
-
Multifocal_Breast_Project
Study
EGAS00001000004
-
Myeloproliferative_Neoplasms__MPN__Exome_Validation_Study
Study
EGAS00001000404
-
CMF_RNA_sequencing
Study
EGAS00001000470
-
CIRCLE-seq of PDAC PDO
Study
EGAS50000000194
-
TSG_knock_out_in_hiPSCs
Study
EGAS00001002262
-
DMET Genes, Nicotine Metabolism and Prospective Abstinence
Study
phs000931
-
NRG-GY017: Atezolizumab before and/or with Chemoradiotherapy in Immune System Activation in Patients with Node Positive Stage IB2, II, IIIB, or IVA Cervical Cancer
Study
phs003833
-
Genome-Wide Predictors of Treatment-Related Toxicities in SWOG S0221 Trial
Study
phs001428
-
A Pilot Study of NKTR-214 and Nivolumab in Selected Patients with Locally Advanced/Metastatic Sarcoma
Study
phs002852
-
Genomic Profiling of Relapsed and Refractory Childhood Cancers
Study
phs002238
-
Single cell analysis reveals new evolutionary complexity in uveal melanoma
Study
phs001861
-
Transcriptomic and Epigenetic Profiling of SCLC Patient Samples
Study
phs003416
-
Whole-exome sequencing of Helicobacter pylori-uninfected normal gastric gland
Study
JGAS000313
-
Genomic landscape of poorly differentiated thyroid carcinoma
Study
EGAS50000001134