Results 71 to 80 of about 946 (139)
<p>Supplementary Tables S1-S3. List of chromoplectic structural variants, including chromosomal coordinates, event type, and annotated genes/genomic regions, in cases with EWSR1::FLI1 (Table S1), EWSR1::ERG (Table S2), EWSR1::WT1 (Table S3) driver fusions, and longitudinal/sequencing samples from patients with EWSR1::FLI1 or EWSR1::WT1 driver ...
Cristina R. Antonescu +8 more
openaire +1 more source
Patterns and mechanisms of structural variations in human cancer
Next-generation sequencing technology has enabled the comprehensive detection of genomic alterations in human somatic cells, including point mutations, chromosomal rearrangements, and structural variations (SVs).
Kijong Yi, Y. Ju
semanticscholar +1 more source
<div>Abstract<p>Chromoplexy is a phenomenon defined by large-scale chromosomal chained rearrangements. A previous study observed chromoplectic events in a subset of Ewing sarcomas (ES), which was linked to an increased relapse rate. Chromoplexy analysis could potentially facilitate patient risk stratification, particularly if it could be ...
Cristina R. Antonescu +8 more
openaire +1 more source
High-resolution copy-number mutational signatures for ovarian cancer patient stratification
During tumour evolution, diverse mutational processes can affect copy number state across the genome, by deleting or duplicating sections of genomic material.
Mattocks, Joanne
core +1 more source
Roles of somatic mutations in STAG2, TP53 and CDKN2A and chromoplexy in Ewing sarcoma oncogenesis
Le sarcome d'Ewing est le second cancer pédiatrique des os et tissus mous le plus fréquent. Il est caractérisé par la présence d'une translocation chromosomique fusionnant un gène de la famille FET à un facteur de transcription de la famille des ETS ...
Heintzé, Maxime
core
Whole-genome sequencing of human malignant mesothelioma tumours and cell lines
Pleural mesothelioma is a cancer of serosal surfaces caused by environmental exposure to asbestos. Clinical outcome remains poor and while trials of new treatments are ongoing it remains an understudied cancer.
Bowman, Rayleen V. +9 more
core +1 more source
Complex Chromosomal Rearrangements (CCRs) are increasingly being reported as genetic risk factors of clinical significance in cancer owing to their identification using high resolution whole genome profiling technologies.
Rani, Lata +8 more
core +1 more source
Plenary Abstracts Session & Oral Presentations
HemaSphere, Volume 9, Issue S1, June 2025.
wiley +1 more source

