A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patients
- DOI
- 10.1093/nargab/lqae033
- Published
- 2024-04-04
- Container
- NAR Genomics and Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1093/nargab/lqae033,
title = {A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patients},
author = {Andrea Bianchi and Veronica Zelli and Andrea D’Angelo and Alessandro Di Matteo and Giulia Scoccia and Katia Cannita and Antigone S Dimas and Stavros Glentis and Francesca Zazzeroni and Edoardo Alesse and Antinisca Di Marco and Alessandra Tessitore},
year = {2024},
journal = {NAR Genomics and Bioinformatics},
doi = {10.1093/nargab/lqae033},
url = {https://doi.org/10.1093/nargab/lqae033}
}RIS
TY - JOUR TI - A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patients AU - Andrea Bianchi AU - Veronica Zelli AU - Andrea D’Angelo AU - Alessandro Di Matteo AU - Giulia Scoccia AU - Katia Cannita AU - Antigone S Dimas AU - Stavros Glentis AU - Francesca Zazzeroni AU - Edoardo Alesse AU - Antinisca Di Marco AU - Alessandra Tessitore PY - 2024 JO - NAR Genomics and Bioinformatics DO - 10.1093/nargab/lqae033 UR - https://doi.org/10.1093/nargab/lqae033 ER -
APA
Bianchi, A., Zelli, V., D’Angelo, A., Matteo, A. D., Scoccia, G., Cannita, K., Dimas, A. S., Glentis, S., Zazzeroni, F., Alesse, E., Marco, A. D., & Tessitore, A. (2024). A method to comprehensively identify germline SNVs, INDELs and CNVs from whole exome sequencing data of BRCA1/2 negative breast cancer patients. NAR Genomics and Bioinformatics. https://doi.org/10.1093/nargab/lqae033
Source records
- crossref · retrieved 2026-09-26T12:48:54.108Z