Study results demonstrate that combining copy number variation (CNV) information with cfDNA fragment size information could serve as a new avenue for early detection of colorectal cancer, with ...

PURPOSESomatic chromosomal alterations, particularly monosomy 3 and 8q gains, have been associated with metastatic risk in uveal melanoma (UM). Whole genome-scale evaluation of detectable alterations ...

Array comparative genomic hybridization has helped characterize copy-number variations and advanced research in many biomedical areas.

Identification and detection of structural variations (SVs), copy number variations (CNVs), and tandem repeat expansions/contractions has been the standard of care (SOC) for the detection and ...

Mission Bio Launches Innovative Single-cell Genome Integrity Solution to Measure Whole Genome Copy Number Variation in Advanced Therapies and Tumor Samples ...

Over 250 associations between phenotype and copy number variation were identified. New ties were revealed between certain genes and various traits, like height. For example, some carriers of very rare ...