Short-Read Sequencing Detects Large Structural Variants in Cancer Genomes

Cancer Discov. 2024 Jan 12;14(1):16. doi: 10.1158/2159-8290.CD-RW2023-186.

Abstract

Most large structural variants (SV) can be detected by short-read sequencing (SRS) of cancer genomes.

MeSH terms

  • Genomic Structural Variation*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Neoplasms* / genetics
  • Sequence Analysis, DNA