Clinical Validation of the Belay Ascent™ Test to Report on Chromosomal Arm-Level Aneuploidy and Gene-Level Copy Number Variants in Cerebrospinal Fluid Using Low-Pass Whole-Genome Sequencing
- DOI
- 10.3390/cancers18081277
- Published
- 2026-04-17
- Container
- Cancers
- Publisher
- MDPI AG
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3390/cancers18081277,
title = {Clinical Validation of the Belay Ascent™ Test to Report on Chromosomal Arm-Level Aneuploidy and Gene-Level Copy Number Variants in Cerebrospinal Fluid Using Low-Pass Whole-Genome Sequencing},
author = {Qian Nie and Kala F. Schilter and Alexandra Larson and Vindhya Udhane and Viriya Keo and Sakshi Khurana and Jennifer N. Adams and Anthony Acevedo and Daniel Sanchez and Tarin Peltier and Kathleen Mitchell and DeElegant Robinson and Kyle M. Hernandez and Christopher Douville and Chetan Bettegowda and Honey V. Reddi},
year = {2026},
journal = {Cancers},
doi = {10.3390/cancers18081277},
url = {https://doi.org/10.3390/cancers18081277}
}RIS
TY - JOUR TI - Clinical Validation of the Belay Ascent™ Test to Report on Chromosomal Arm-Level Aneuploidy and Gene-Level Copy Number Variants in Cerebrospinal Fluid Using Low-Pass Whole-Genome Sequencing AU - Qian Nie AU - Kala F. Schilter AU - Alexandra Larson AU - Vindhya Udhane AU - Viriya Keo AU - Sakshi Khurana AU - Jennifer N. Adams AU - Anthony Acevedo AU - Daniel Sanchez AU - Tarin Peltier AU - Kathleen Mitchell AU - DeElegant Robinson AU - Kyle M. Hernandez AU - Christopher Douville AU - Chetan Bettegowda AU - Honey V. Reddi PY - 2026 JO - Cancers DO - 10.3390/cancers18081277 UR - https://doi.org/10.3390/cancers18081277 ER -
APA
Nie, Q., Schilter, K. F., Larson, A., Udhane, V., Keo, V., Khurana, S., Adams, J. N., Acevedo, A., Sanchez, D., Peltier, T., Mitchell, K., Robinson, D., Hernandez, K. M., Douville, C., Bettegowda, C., & Reddi, H. V. (2026). Clinical Validation of the Belay Ascent™ Test to Report on Chromosomal Arm-Level Aneuploidy and Gene-Level Copy Number Variants in Cerebrospinal Fluid Using Low-Pass Whole-Genome Sequencing. Cancers. https://doi.org/10.3390/cancers18081277
Source records
- crossref · retrieved 2026-09-27T06:57:16.173Z