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CNV Detection from Circulating Tumor DNA in Late Stage Non-Small Cell Lung Cancer Patients
While methods for detecting SNVs and indels in circulating tumor DNA (ctDNA) with hybridization capture-based next-generation sequencing (NGS) have been available, copy number variations (CNVs) detection is more challenging. Here, we present a method enabling CNV detection from a 150-gene panel usin...
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| Publicado no: | Genes (Basel) |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6895974/ https://ncbi.nlm.nih.gov/pubmed/31739500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes10110926 |
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