-
Resident memory CD8 T cell in human lung cancer
Study
EGAS00001004707
-
WGS of 32 paired SRCC samples
Study
EGAS00001002668
-
Epigenome and transcriptome profiling of chronic lymphocytic leukemia patients
Study
EGAS00001001821
-
QSEA – modelling of genome-wide DNA methylation from sequencing enrichment experiments
Study
EGAS00001001822
-
Mutation-specific non-canonical pathway of PTEN as a distinct therapeutic target for glioblastoma
Study
EGAS00001004753
-
Identification of 19 novel loci reveals gene regulatory mechanisms determining susceptibility to testicular germ cell tumour
Study
EGAS00001001836
-
Whole exome sequencing of Finnish hereditary breast cancer families
Study
EGAS00001001835
-
Genome-wide quantification of rare somatic mutations in normal human tissues using massively parallel sequencing
Study
EGAS00001001838
-
CancerLocator: Non-Invasive Cancer Diagnosis and Tissue-of-Origin Prediction Using Methylation Profiles of Cell-Free DNA
Study
EGAS00001002211
-
Tumor HTG EdgeSeq from metastatic castrate resistant prostate cancer
Study
EGAS00001004852
-
Sequencing of liver cancer cell lines
Study
EGAS00001002237
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
EAC Genomic data
Study
EGAS00001004887
-
Circulating Tumor DNA Analysis Detects Minimal Residual Disease and Predicts Recurrence in Patients with Stage II Colon Cancer
Study
EGAS00001001839
-
Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients
Study
EGAS00001004975
-
Longitudinal single-cell RNA-seq data of metastatic ovarian cancer
Study
EGAS00001005006
-
RNA sequencing of PTCL-NOS
Study
EGAS00001005015
-
Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data
Study
EGAS00001000659
-
Stromal cell diversity associated with immune evasion in human triple‐negative breast cancer
Study
EGAS00001005061
-
Subtype specific progression from DCIS to invasive breast cancer
Study
EGAS00001001866
-
Targeted next-generation sequencing of 13 chordoid gliomas of the third ventricle
Study
EGAS00001002733
-
early-Duodenal Cancer sequencing study
Study
EGAS00001006357
-
H021-Master Umbrella study2 (not to be released)
Study
EGAS00001005145
-
Multi-omics analysis of primary glioblastoma cell-lines shows recapitulation of pivotal molecular features of parental tumors
Study
EGAS00001001871
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
Analysis of Multiparametric MR imaging and tumor tissue sampling to identify response and acquired resistance to HIF-2 inhibition in patients with advanced clear cell renal cell carcinoma enrolled in a phase 1, multiple-dose, dose-escalation trial of PT2385, a HIF-2alpha inhibitor
Study
EGAS00001003506
-
Genomic and Transcriptomic Profile of Paired Primary-Metastasis Colorectal Tumors
Study
EGAS00001005276
-
ChIP-seq in colorectal cancer and paired adjacent normal mucosa
Study
EGAS00001005303
-
Whole exome sequencing data of germline and two independent primary leukemias of five patients
Study
EGAS00001001889
-
Evolutionary analysis of primary tumors and metastatic lesions from 20 breast cancer patients (99 samples in total) using exome sequencing data.
Study
EGAS00001002737
-
NOWAC blood-based breast cancer case-control study
Study
EGAS00000000134
-
Identification_and_functional_validation_of_driver_mutations_in_colorectal_cancer
Study
EGAS00001000044
-
Analysis_of_genomic_integrity_of_disease_corrected_human_induced_pluripotent_stem_cells_by_exome_sequencing
Study
EGAS00001000055
-
Whole Exome Sequencing of Localized Prostate Cancer Patients
Study
EGAS00001005685
-
Contribution of allelic imbalance to colorectal cancer
Study
EGAS00001002966
-
Screening_for_human_epigenetic_variation_at_CpG_islands
Study
EGAS00001000074
-
Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single nucleotide variants and tumoral heterogeneity by massively parallel sequencing
Study
EGAS00001000370
-
Screening_for_abnormal_CGI_methylation_in_primary_colorectal_tumours
Study
EGAS00001000076
-
DNA methylation and Panel sequencing for pancreatic neuroendocrine carcinomas (PanNECs) and pancreatic neuroendocrine tumors (PanNETs)
Study
EGAS00001005731
-
Whole-exome sequencing of human pancreatic cancers and characterization of genomic instability caused by MLH1 haploinsufficiency and complete deficiency
Study
EGAS00001000149
-
'Targeted High Throughput Sequencing in Clinical Cancer Settings: Formaldehyde fixed-paraffin embedded (FFPE) tumor tissues, input amount and tumor heterogeneity'
Study
EGAS00001000136
-
The genomic landscape of large and small tumors in early-onset prostate cancer patients
Study
EGAS00001000383
-
Exome Sequencing of Gastric Cancer
Study
EGAS00001000153
-
Complete Genomics paired end sequencing; Ovarian cancer
Study
EGAS00001000158
-
Whole genome sequencing of matched primary and metastatic acral melanomas
Study
EGAS00001000169
-
The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.
Study
EGAS00001005827
-
Integrative analysis of small cell lung cancer
Study
EGAS00001000299
-
Whole-exome Sequencing Combined with Functional Genomics Reveals Novel Candidate Driver Cancer Genes in Endometrial Cancer
Study
EGAS00001000318
-
Inferring tumor genomes from peripheral blood i.e. CTCs and plasma-DNA using deep sequencing and targeted enrichment
Study
EGAS00001000337
-
Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma
Study
EGAS00001000369
-
Tumor suppressor miR-133a modulates the prostate cancer epigenome by repressing BAZ2A
Study
EGAS00001000568
-
Plasma-Seq of patients with metastatic prostate cancer
Study
EGAS00001000451
-
Identification of mutations and structural rearrangements in plasma DNA form metastatic prostate cancer patients
Study
EGAS00001000453
-
Patient-derived organoids_Vumc
Study
EGAS00001005947
-
Comprehensive analysis of atypical teratoid rhabdoid tumour (ATRT) using genomic, epigenomic and transcriptomic techniques.
Study
EGAS00001000506
-
DNA from colon cancer samples and matched normal samples was hybridized on Human 660W-Quad SNP arrays and sequenced in Illumina HiScanSQ.
Study
EGAS00001000558
-
Mutational analysis reveals the origin and therapy-driven evolution of recurrent glioma
Study
EGAS00001000579
-
Resistance to anti-EGFR therapy in colorectal cancer
Study
EGAS00001000582
-
Assessment of genomic copy number alterations in breast cancer
Study
EGAS00001000585
-
Genome-wide analysis of HPV integration in human cancers reveals recurrent, focal genomic instability
Study
EGAS00001000599
-
These are from Korean HCC samples with exome sequencing
Study
EGAS00001000604
-
Whole Genome Sequencing of Asian Lung Cancers: Second Hand Smoke is Not Responsible for Higher Incidence of Lung Cancer Among Asian Never-Smokers
Study
EGAS00001000621
-
Divergence between high metastatic tumor burden and low circulating tumor DNA concentration in metastasized breast cancer
Study
EGAS00001000625
-
A Genomics-Based Classification of Human Lung Tumors
Study
EGAS00001000647
-
CD74-NRG1 fusions in lung adenocarcinoma
Study
EGAS00001000653
-
Integrated genomic characterization of adrenocortical carcinoma
Study
EGAS00001000665
-
An oncogenic enhancer-rearrangement causes concomitant deregulation of EVI1 and GATA2 in leukemia. Targeted resequencing of chromosomal regions centered on 3q21 and 3q26 in conjunction with RNA-Seq from Acute Myeloid Leukemia patients.
Study
EGAS00001000669
-
Recurrent epimutations activate gene body promoters in primary glioblastoma
Study
EGAS00001000685
-
Pheno-Seq, linking 3D phenotypes of clonal tumor spheroids to gene expression
Study
EGAS00001002999
-
Impact of mutational profiles on response of primary oestrogen receptor-positive breast cancers to oestrogen deprivation
Study
EGAS00001001940
-
Validation of a targeted sequencing panel for multiple myeloma
Study
EGAS00001006164
-
Whole-genome sequencing of bladder cancers of various stages and grades to search for driver mutations, chromosome-scale somatic changes, mutation signatures and clonal structures.
Study
EGAS00001000738