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Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
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Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
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Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
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DERMATLAS__Porocarcinoma_WES
Study
EGAS00001005720
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Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Study
EGAS00001005737
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Exome sequencing
Study
EGAS00001005761
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Genetic and immune landscape evolution defines subtypes of MMR deficient colorectal cancer
Study
EGAS00001005769
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Gene expression-based prediction of pazopanib efficacy in sarcoma (HIPO, H021)
Study
EGAS00001005836
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Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
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The European MAPPYACTS trial: Precision Medicine Program in Pediatric and Adolescent Patients with Recurrent Malignancies
Study
EGAS00001005935
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Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001005945
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Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Study
EGAS00001005982
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Host genotyping data from Dutch adult bacterial meningitis patients and linked bacterial genome sequences
Study
EGAS00001005993
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Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab
Study
EGAS00001006004
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Human genome-wide variations in the Massim region
Study
EGAS00001006010
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Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq)
Study
EGAS00001006017
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Long-term temporal stability of peripheral blood DNA methylation alterations in patients with inflammatory bowel disease.
Study
EGAS00001006501
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Neuroblastoma Evolution
Study
EGAS00001006533
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Insights from genome-wide data from Thailand and Laos
Study
EGAS00001006053
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Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058
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Genetics of non-syndromic idiopathic autism spectrum disorders in India
Study
EGAS00001006060
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High-throughput telomere length measurement at nucleotide resolution using the PacBio high fidelity sequencing platform
Study
EGAS00001006103
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Genomic History of the Solomon Islands
Study
EGAS00001006116
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Conserved features of TERT promoter duplications reveal an activation mechanism that mimics hotspot mutations in cancer
Study
EGAS00001006118
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Genetic immune escape landscape in primary and metastatic cancer
Study
EGAS00001006123