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Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
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Defining the metastasome in colorectal cancer: Implications for hypotheses on metastasis evolution and personalized therapy (HIPO-032)
Study
EGAS00001002717
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Partner-independent fusion gene detection by multiplexed CRISPR/Cas9 enrichment and long-read Nanopore sequencing
Study
EGAS00001003964
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Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
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Exploration of CNV’s and SNV’s in cancers with well-known genetic rearrangements: Identification of additional genetic changes in rearrangements-driven cancer
Study
EGAS00001000673
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Breast_Heterogeneity_Validation
Study
EGAS00001001972
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Recurrent DNMT3B gene rearrangements are associated with unfavorable outcome in dicentric (9;20)-positive pediatric BCP-ALL
Study
EGAS00001007383
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Genomic consequences of aberrant DNA repair mechanisms stratify ovarian cancer histotypes
Study
EGAS00001002390
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Analysis of the Elements Involved in the Enrichment of a Panel of Genomic Regions by Nanopore Sequencing Using Adaptive Sampling
Study
EGAS00001007375
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Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib
Study
EGAS00001004539
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A whole genome analysis of single fetal human stem cells from the liver and the intestine
Study
EGAS00001002886
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A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome
Study
EGAS00000000052
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Massive Genomic Rearrangment Acquired in a Single Catastrophic Event During Cancer Development
Study
EGAS00000000029
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G&T-seq: parallel sequencing of the genomes and transcriptomes of single cells
Study
EGAS00001001204
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An integrative model of pathway convergence in genetically heterogeneous blast crisis chronic myeloid leukemia (CML)
Study
EGAS00001001751
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Identification of the dismal subtype of B-ALL with dysregulation of CDX2 and UBTF
Study
EGAS00001005863
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Distinct evolutionary trajectories of primary high grade serous ovarian cancers revealed through spatial mutational profiling
Study
EGAS00001000547
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Whole_genome_sequencing_of_100_DDD_trios_with_suspected_noncoding_causal_mutations
Study
EGAS00001002452
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Genomic Profiling of Pediatric Tumors by Cell Free DNA Sequencing
Study
EGAS50000000072
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One-step generation of tumor models by base editor multiplexing in adult stem cell-derived organoids
Study
EGAS00001006886
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Whole genome characterisation of lung cancer organoids and tissue
Study
EGAS00001002899
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Epigenomic data of HEMa_LP
Study
EGAS00001004016
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A small cell lung cancer genome reports complex tobacco exposure signatures
Study
EGAS00000000051
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Genome sequencing identifies splice-disrupting variants in childhood heart disease
Study
EGAS50000000586
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Multiplexing cortical brain organoids for the longitudinal dissection of developmental traits at single cell resolution
Study
EGAS50000000698