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DNA WGS Short Read Sequence (Illumina NovaSeq) for manuscript titled: "Performance of Somatic Structural Variant Calling in Lung Cancer using Oxford Nanopore Sequencing Technology"
Dataset
EGAD00001015399
-
DNA WGS Long Read Sequence (PromethION) for manuscript titled: "Performance of Somatic Structural Variant Calling in Lung Cancer using Oxford Nanopore Sequencing Technology"
Dataset
EGAD00001015400
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Paediatric_CNS_tumour_autopsy_DNA
Study
EGAS00001004771
-
Spatiotemporal evolution and inter-patient heterogeneity in primary and recurrent/metastatic head and neck squamous cell carcinoma
Study
EGAS00001007464
-
Evaluation of EBUS-TBNA Aspirates from Advanced NSCLC for Comprehensive Sequencing Platforms Including Whole Genome Sequencing
Study
EGAS00001007708
-
Benchmarking for alignment and variant calling
Study
EGAS00001007819
-
Whole Genome Sequence and RNASeq Samples for Lung Cancer
Study
EGAS00001007832
-
Whole exome and transcriptome sequencing of biliary tract cancer
Study
EGAS00001000950
-
Single-cell transcriptome sequencing of regulatory and conventional T cells in breast cancer patients and healthy individuals.
Study
EGAS00001002933
-
Identification of HER2-positive breast cancer molecular subtypes with potential clinical implications in the ALTTO clinical trial
Study
EGAS50000000525