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Genomicsena-DATASET-LUMC-SASC-04-12-2017-12:12:33:008-298 - samples
Patient information SSc patients were recruited at the Department of Rheumatology of the Leiden University Medical Center (Leiden, The Netherlands). All patients met the American Rheumatism Association classification criteria for SSc (Subcommittee for scleroderma criteria 1980), and were classified ...
EGAD00001003832 | EGA
Genomicsena-DATASET-VUMC-CCA-26-05-2021-09:58:48:372-433 - samples
Control cohort of lymphoma samples sequenced with a hybrid capture panel designed to be able to detect translocations and mutations in lymphoma samples. used in the paper "Robust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing"
EGAD00001007711 | EGA
GenomicsRobust detection of translocations in lymphoma FFPE samples using Targeted Locus Capture-based sequencing - NGS targeted capture control cohort
In routine diagnostic pathology, cancer biopsies are preserved by Formalin-Fixed, Paraffin-Embedding (FFPE) procedures for examination of (intra-) cellular morphology. Such procedures inadvertently induce DNA fragmentation, which compromises sequencing-based analyses of chromosomal rearrangements. Y...
EGAS00001005325 | EGA
GenomicsAntisense long non-coding RNAs are deregulated in skin tissue of patients with systemic sclerosis
Systemic sclerosis (SSc) is an autoimmune disease characterized by fibrosis of skin and multiple organs of which the pathogenesis is poorly understood. Here we studied differentially expressed coding and non-coding genes in relation to SSc pathogenesis with a specific focus on antisense non-coding R...
EGAS00001002751 | EGA
GenomicsDAC: Antisense long non-coding RNAs are deregulated in skin tissue of patients with systemic sclerosis
Data Access Committee EGAC00001000788
EGAC00001000788 | EGA
TranscriptomicsPrediction of isolated central nervous system relapses in pediatric acute lymphoblastic leukemia
Background In childhood acute lymphoblastic leukemia (ALL), central nervous system (CNS) involvement is rare at diagnosis (1-4%), but more frequent at relapse (~30%). Minimal residual disease diagnostics predict most bone marrow (BM) relapses, but likely cannot predict isolated CNS relapses. Cons...
ORGANISM(S): Homo sapiens 
2015-12-31 | E-GEOD-60926 | biostudies-arrayexpress
UnknownValue of risk scores in the decision to palliate patients with ruptured abdominal aortic aneurysm.
Not available
S-EPMC6055637 | biostudies-literature
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