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Genome and transcriptome sequence data from a metastatic melanoma patient
Dataset
EGAD00001004653
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Genome and transcriptome sequence data from a metastatic colorectal cancer patient
Dataset
EGAD00001004646
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Clinical Implications of Genomic Alterations in the Tumour and Circulation of Pancreatic Cancer Patients
Dataset
EGAD00001001421
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ICR639 CPG NGS Validation series
Dataset
EGAD00001004134
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Next generation sequencing of liver cancer cell lines
Dataset
EGAD00001003165
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Congenital mesoblastic nephroma and infantile fibrosarcoma
Dataset
EGAD00001003885
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Prostate WGS data (late onset)
Dataset
EGAD00001003290
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Genome and transcriptome sequence data from a lung cancer patient
Dataset
EGAD00001002023
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Whole Exome Sequencing of 60 tumor/normal matched liver Cancers (HCC)
Dataset
EGAD00001004180
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Whole exome sequencing data of tumor/normal pairs for the study "TGF-β attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells"
Dataset
EGAD00001004218
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Genome and transcriptome sequence data from a metastatic breast cancer patient
Dataset
EGAD00001003731
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Genome and transcriptome sequence data from a left cavernous sinus invasive skull meningioma patient
Dataset
EGAD00001003662
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Evolution and clinical impact of genetic epistasis within EGFR-mutant lung cancers: multi-timepoint exome sequencing of a single patient's disease
Dataset
EGAD00001003769
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Whole Genome Sequencing for Korean Diffuse Gastric Cancer
Dataset
EGAD00001003953
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Genome and transcriptome sequence data from a metastatic leiomyosarcoma patient
Dataset
EGAD00001004639
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Targeted Pulldown Validation of mutations found in whole genome sequencing
Dataset
EGAD00001001061
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Deep amplicon sequencing to infer malignant clonal populations for The interface of malignant and immunologic clonal dynamics in high-grade serous ovarian cancer
Dataset
EGAD00001003986
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Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Dataset
EGAD00001000850
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SPECTA: NGS Screening Program for Efficient Clinical Trial Access
Dataset
EGAD00001000894
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Structural rearrangements generate cell-specific, gene-independent CRISPR-Cas9 loss of fitness effects.
Dataset
EGAD00001004124
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The evolving mutational landscape of normal human esophagus
Dataset
EGAD00001004158
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ICGC Korean Breast Cancer Project
Dataset
EGAD00001001322
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ChIP-Seq (H3K4me1) assays for reference epigenomes generated by Centre for Epigenome Mapping Technologies at Canada's Michael Smith Genome Sciences Centre, BC Cancer Agency, as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001232
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Fastq data for ChIP-Seq (H3K36me3) assays for reference epigenomes generated at Centre for Epigenome Mapping Technologies, Genome Sciences Center, B.C. Cancer Agency as part of the International Human Epigenome Consortium.
Dataset
EGAD00001001405
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Genome and transcriptome sequence data from a GI primary (prev breast cancer) patient
Dataset
EGAD00001002979