-
Decoding Human Heart Morphogenesis through Single-cell Multi-modal Analyses
Study
phs002031
-
Parallel CRISPR Editing of Familial ALS Mutations Into a Healthy Control iPSC Line
Study
phs002440
-
Non-Coding Autoimmune Risk Variant Defines Role for ICOS in T Peripheral Helper Cell Development
Study
phs003448
-
Kids First and INCLUDE: Down Syndrome, Heart Defects, and Acute Lymphoblastic Leukemia
Study
phs002330
-
Natural Killer Cell Therapies for Hematologic Malignancies
Study
phs002681
-
WGoxBS and SureSelect data of the POPS placenta samples
Dataset
EGAD00001003136
-
Mutational landscape of normal epithelial cells in Lynch Syndrome patients
Dataset
EGAD00001008092
-
Clinical outcomes and immune correlates of response to nivolumab plus chemoradiotherapy in women with locally-advanced cervical cancer – NiCOL study
Study
EGAS00001007297
-
Spatiotemporal Genomic Profiling of Intestinal Metaplasia Reveals Clonal Dynamics of Gastric Cancer Progression
Study
EGAS00001007067
-
Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Study
EGAS00001004013
-
Comprehensive genomic profiles of small cell lung cancer
Study
EGAS00001000925
-
Clonal haematopoiesis in patients with AAA (2019-04-03)
Dataset
EGAD00001004895
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-010
Dataset
EGAD00001006026
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-009
Dataset
EGAD00001006027
-
Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell renal cell carcinoma -- CA209-025
Dataset
EGAD00001006029
-
Single-cell RNA-sequencing of CD34+ bone marrow cells from patients with SLE, healthy individuals and umbilical cord blood samples
Study
EGAS00001007317
-
A common single nucleotide variant in T is strongly associated with chordoma
Dataset
EGAD00001000226
-
Targeted sequencing of genes recurrently mutated in AML - part2
Dataset
EGAD00001000747
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000794
-
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000850
-
Mutational Signatures of relapse in rectal cancer FFPE samples in the CR07 clinical trial
Dataset
EGAD00001000875
-
Raw sequencing data - Intra-tumor heterogeneity and clonal evolution patterns towards platinum-resistant high-grade serous ovarian cancer
Dataset
EGAD00001001381
-
Amplicon-based sequencing of drug resistant lung cancer cell lines (2017-07-05)
Dataset
EGAD00001003425
-
WES of blood and patient-matched cecum tumor tissue samples, Panel NGS of patient-matched cfDNA
Dataset
EGAD00001005737
-
WES data from 165 tumor/germline samples with muscle invasive bladder cancer.
Dataset
EGAD00001006239
-
Genomic Rearrangements in Pediatric Cancer
Dataset
EGAD00001007701
-
Dataset for head_and_neck_cancer-EXON
Dataset
EGAD00001008880
-
Dataset for neuroendocrine_adrenal_tumor-WHOLE_GENOME
Dataset
EGAD00001008893
-
WGS of primary mesothelioma cell lines
Dataset
EGAD00001009641
-
Whole genome sequencing data of high-grade serous ovarian cancer samples (set 2)
Dataset
EGAD00001009791
-
CPC-GENE primary prostate benign and tumour tissue Hi-C sequencing reads
Dataset
EGAD00001008024
-
MutWP5: CRUK Mutographs of Cancer: Breast: Reduction Mammoplasty (Exome)
Dataset
EGAD00001010110
-
MutWP5: CRUK Mutographs of Cancer: Breast: Reduction Mammoplasty (WG)(Novaseq)
Dataset
EGAD00001010113
-
MutWP5: CRUK Mutographs of Cancer: Breast: Reduction Mammoplasty (Exome)(Novaseq)
Dataset
EGAD00001010116
-
Ither2 WXS dataset - Implementation of pediatric precision oncology into clinical practice: The individualized Therapies for Children with cancer program “iTHER”
Dataset
EGAD00001010178
-
Bottleneck_Sequencing_Of_Human_Tissue__Wgs_
Study
EGAS00001004066
-
Melanoma_brain_metastases
Study
EGAS00001002107
-
ENU_HT_29_BRAF_Triple_Therapy_Clones
Study
EGAS00001001778
-
V2_panel_bait_design_test
Study
EGAS00001001780
-
Keratinocyte_CRISPR_screens
Study
EGAS00001002714
-
Melanoma_post_mortem_analysis
Study
EGAS00001003531
-
Radiotherapy_induced_Sarcoma_exome
Study
EGAS00001000194
-
Signatures of mismatch repair deficiency in cancer genomes
Study
EGAS00001000182
-
EORTC RP1335 SPECTA Lung cancer data
Study
EGAS00001004485
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-4)
Study
EGAS00001006101
-
Exomes of High-risk Prostate cancer
Study
EGAS00001001015
-
Whole genome sequencing of colorectal cancer patients (SG-BULK-1)
Study
EGAS00001006030
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-2)
Study
EGAS00001006039
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-3)
Study
EGAS00001006056
-
Whole Genome sequencing of colorectal cancer patients (SG-BULK-5)
Study
EGAS00001006114