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Applying low coverage whole genome sequencing to detect malignant ovarian mass
To evaluate whether low coverage whole genome sequencing is suitable for the detection of malignant pelvic mass and compare its diagnostic value with traditional tumor markers. We enrolled 63 patients with a pelvic mass suspicious for ovarian malignancy. Each patient underwent low coverage whole gen...
Autores principales: | Chen, Ming, Zhong, Pengqiang, Hong, Mengzhi, Tan, Jinfeng, Yu, Xuegao, Huang, Hao, Ouyang, Juan, Lin, Xiaoping, Chen, Peisong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394143/ https://www.ncbi.nlm.nih.gov/pubmed/34446054 http://dx.doi.org/10.1186/s12967-021-03046-3 |
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