Panel-based next-generation sequencing with copy number variant detection pipeline could increase the detection rate of hereditary colorectal cancer syndrome compared with Sanger sequencing
- DOI
- 10.1186/s13053-026-00350-1
- Published
- 2026-08-07
- Container
- Hereditary Cancer in Clinical Practice
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s13053-026-00350-1,
title = {Panel-based next-generation sequencing with copy number variant detection pipeline could increase the detection rate of hereditary colorectal cancer syndrome compared with Sanger sequencing},
author = {Joonsang Yu and Jaeyeon Ryu and Sollip Kim and Jihun Kim and Yong Sang Hong and Woochang Lee and Seok-Byung Lim and Jeong-Sik Byeon and Sail Chun},
year = {2026},
journal = {Hereditary Cancer in Clinical Practice},
doi = {10.1186/s13053-026-00350-1},
url = {https://doi.org/10.1186/s13053-026-00350-1}
}RIS
TY - JOUR TI - Panel-based next-generation sequencing with copy number variant detection pipeline could increase the detection rate of hereditary colorectal cancer syndrome compared with Sanger sequencing AU - Joonsang Yu AU - Jaeyeon Ryu AU - Sollip Kim AU - Jihun Kim AU - Yong Sang Hong AU - Woochang Lee AU - Seok-Byung Lim AU - Jeong-Sik Byeon AU - Sail Chun PY - 2026 JO - Hereditary Cancer in Clinical Practice DO - 10.1186/s13053-026-00350-1 UR - https://doi.org/10.1186/s13053-026-00350-1 ER -
APA
Yu, J., Ryu, J., Kim, S., Kim, J., Hong, Y. S., Lee, W., Lim, S., Byeon, J., & Chun, S. (2026). Panel-based next-generation sequencing with copy number variant detection pipeline could increase the detection rate of hereditary colorectal cancer syndrome compared with Sanger sequencing. Hereditary Cancer in Clinical Practice. https://doi.org/10.1186/s13053-026-00350-1
Source records
- crossref · retrieved 2026-11-07T12:50:55.223Z