-
Whole-genome landscape of adult T-cell leukemia/lymphoma
Study
EGAS00001005237
-
Organoid_Derivation_Project___GRCh38___RNAseq
Study
EGAS00001004677
-
Genomics analysis of mucinous tumours of the ovary and related neoplasms
Study
EGAS00001003545
-
Single Cell Sperm sequencing try 2
Study
EGAS00001004035
-
Epigenomic data of HEMa_LP
Study
EGAS00001004016
-
RNA-seq of Ewing sarcoma tumors (ICGC)
Study
EGAS00001003333
-
SNP array data for 140 individuals from 5 populations in Pakistan
Study
EGAS00001002965
-
Covid19 WGS BAM files
Study
EGAS00001007048
-
Whole exome sequencing study of cholesteatoma patients from affected families
Study
EGAS00001006147
-
Organoid_Derivation_Project___GRCh38___WGS
Study
EGAS00001004712
-
CD8+ Tumor-Infiltrating Lymphocyte Abundance is a Positive Prognostic Indicator in Nasopharyngeal Cancer
Study
EGAS00001006396
-
Bulk and single-cell AML RNA-seq post ex vivo culture
Study
EGAS00001006265
-
Neuroblastoma Evolution
Study
EGAS00001006533
-
Rifaximin stimulates nitrogen detoxification by PXR-independent mechanisms in human small intestinal organoids
Study
EGAS00001006857
-
DECONVOLUTION OF HEMATOPOIETIC STEM/PROGENITOR CELL SIGNALING IN HUMAN AML
Study
EGAS00001007330
-
Organoid_Derivation_Project___GRCh38___TGS
Study
EGAS00001007349
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90560A
Dataset
EGAD00001004733
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95660A
Dataset
EGAD00001004750
-
SmartSeq2 index cultures
Dataset
EGAD00001008187
-
MPNST_Data
Dataset
EGAD00001006253
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90600C
Dataset
EGAD00001004735
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90706
Dataset
EGAD00001004744
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95632B
Dataset
EGAD00001004748
-
RNA-sequencing
Dataset
EGAD00001004784
-
Exome sequencing of 3 blood samples from tall man and his parents
Dataset
EGAD00001007767
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95670B
Dataset
EGAD00001004754
-
Exome sequencing of control DNA samples from patients with Waldenstrom macroglobulinemia
Dataset
EGAD00001005323
-
SF11949 scRNA-Seq primary oligodendroglioma G3 IDH1 Mutant Male
Dataset
EGAD00001005397
-
Sequencing data for oesophageal and related samples - Ococks, Frankell, Masque Soler et al (ctDNA)
Dataset
EGAD00001006373
-
WGS of NPC268_Tumor and NPC268_Cell_line
Dataset
EGAD00001010292
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A73044B
Dataset
EGAD00001004720
-
Untargeted serum metabolomics profiled by Metabolon Inc.
Dataset
EGAD00001006247
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95724B
Dataset
EGAD00001004757
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96150A
Dataset
EGAD00001004764
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75617A
Dataset
EGAD00001004727
-
WES, ultra-deep sequencing exome and RNAseq data of diseased liver samples
Dataset
EGAD00001004792
-
EATL-II whole-exome sequencing profile
Dataset
EGAD00001002220
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A75616B
Dataset
EGAD00001004725
-
Paired-end RNA-seq analysis of the Hypermutation and Malignant Progression in Low-grade Glioma Patients
Dataset
EGAD00001005387
-
SF11956 scRNA-Seq GBM IDHR132H Wildtype Male
Dataset
EGAD00001005392
-
SF11644 scRNA-Seq primary GBM
Dataset
EGAD00001005393
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A95722A
Dataset
EGAD00001004755
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96139A
Dataset
EGAD00001004762
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96145A
Dataset
EGAD00001004763
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A96156A
Dataset
EGAD00001004765
-
SF10127 snRNA-Seq Primary GBM
Dataset
EGAD00001005403
-
SF11964 snATAC Seq Low Grade Astrocytoma IDHR132H mutant
Dataset
EGAD00001005414
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90553A
Dataset
EGAD00001004728
-
Whole genome sequencing of single cells identifies stochastic aneuploidies, genome replication, states, and clonal repertoires for library A90553C
Dataset
EGAD00001004729
-
A molecular atlas of the human postmenopausal fallopian tube and ovary from single-cell ATAC sequencing
Dataset
EGAD00001010077