-
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
-
RNA-seq from melanoma biopsies
Dataset
EGAD00001009059
-
RRBS melanoma biopsies
Dataset
EGAD00001009060
-
Mechanisms of duodenal adenoma development in familial polyposis syndromes
Study
EGAS00001006561
-
Single-nuclei gene-expression analysis of pheochromocytoma and paraganglioma links tumor subtypes with tumor microenvironment
Dataset
EGAD00001008403
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma WES
Dataset
EGAD00001014787
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyoma RNA
Dataset
EGAD00001014788
-
Characterisation of the genetic landscape of cutaneous leiomyoma and leiomyosarcoma - Leiomyosarcoma WES
Dataset
EGAD00001014789
-
Methylation array data of thymic epithelial tumors (TC, NET, THYM)
Dataset
EGAD00010002355
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Study
EGAS00001007703
-
NOTCH1 fusion genes in pediatric T-cell lymphoblastic lymphoma hallmark a common high-risk subgroup with blood TARC levels as possible biomarker
Dataset
EGAD00001015255
-
UAMS - Myeloma Institute Data Access Committee
Dac
EGAC00001000845
-
Genome-wide discovery of somatic coding and regulatory variants in Diffuse Large B-cell Lymphoma
Study
EGAS00001002936
-
Single-cell atlas of multiple myeloma and precursor diseases
Study
EGAS00001006694
-
Genetic and Functional Drivers of Diffuse Large B Cell Lymphoma
Study
EGAS00001002606
-
whole-genome sequencing in 17 ESCC cases and whole-exome sequencing in 71 cases
Study
EGAS00001000709
-
ICGC Oesophageal adenocarcinoma - tumour samples
Study
EGAS00001000725
-
Whole transcriptome sequencing of 38 follicular lymphoma tumours.
Dataset
EGAD00001009650
-
Whole genome sequencing of 78 follicular lymphoma tumours and matched normals
Dataset
EGAD00001011343
-
Whole-Genome Sequencing of Salivary Gland Adenoid Cystic Carcinoma
Study
EGAS00001002812
-
Exploring germline and somatic mutagenesis in the extended family with germline pathogenic variant in POLD1
Study
EGAS00001006434
-
Array-based methylation analysis of SDHB-deficient pheochromocytoma and paraganglioma
Study
EGAS00001007844
-
A5_SDHB_PCPG_Methylation
Dataset
EGAD00010002667
-
Whole genome sequencing of multiple myeloma patient samples.
Dataset
EGAD00001004452
-
Melanoma post mortem analysis
Dataset
EGAD00001005072
-
RNA-seq of multiple myeloma patient samples
Dataset
EGAD00001004543
-
Paired-end RNA-seq analysis of the Hypermutation and Malignant Progression in Low-grade Glioma Patients
Dataset
EGAD00001005387
-
Paired-end Whole Exome-seq analysis of the Hypermutation and Malignant Progression in Low-grade Glioma Patients
Dataset
EGAD00001005386
-
Melanoma post mortem analysis
Dataset
EGAD00001005421
-
Melanoma multi site metastases
Dataset
EGAD00001005483
-
Melanoma multi site metastases
Dataset
EGAD00001005487
-
MBD4 targeted sequencing in pool experiment
Dataset
EGAD00001006989
-
Whole genome bisulfite sequencing on 10 multiple myeloma cases
Dataset
EGAD00001007821
-
Neuroblastoma sequencing data
Dataset
EGAD00001008120
-
MBD4 targeted sequencing
Study
EGAS00001005012
-
Whole genome bisulfite sequencing on 10 multiple myeloma cases
Study
EGAS00001004346
-
Neuroblastoma sequencing data
Study
EGAS00001005602
-
Melanoma post mortem analysis
Dataset
EGAD00010001717
-
Integrated genomic, transcriptional and epigenomic analyses in germinal center-cell lymphomas link the mutation landscape with differential DNA methylation in Burkitt lymphoma
Study
EGAS00001001067
-
HYPERMUTATION AND MALIGNANT PROGRESSION IN LOW-GRADE GLIOMA PATIENTS
Study
EGAS00001002368
-
Whole genome sequencing of multiple myeloma identifies novel structural and non-coding mutations.
Study
EGAS00001003164
-
RNA sequencing of multiple myeloma identifies genes dysregulated by structural variants.
Study
EGAS00001003411
-
noninvasive lung cancer subtyping
Study
EGAS00001007717
-
Oesophageal adenocarcinoma RNAseq from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009399
-
Oesophageal adenocarcinoma WGS from LUD2015-005 study (NCT02735239, EudraCT 2015-005298-19)
Dataset
EGAD00001009400
-
A Risk Score Incorporating Low Pass Whole Genome Sequencing of Cell Free DNA from Patients Receiving CD19 CAR T-Cell Therapy for Large B-Cell Lymphoma
Study
EGAS00001006308
-
Low Pass Whole Genome Sequencing of Cell Free DNA from Patients Receiving CD19 CAR T-Cell Therapy for Large B-Cell Lymphoma
Dataset
EGAD00001009175
-
MD Anderson Lymphoma & Myeloma Data Access Committee
Dac
EGAC00001002706
-
Machine learning guided signal enrichment for ultrasensitive plasma tumor burden monitoring
Study
EGAS00001007545