DEEPGEN(TM)—A Novel Variant Calling Assay for Low Frequency Variants

Detection of genetic variants in clinically relevant genomic hot-spot regions has become a promising application of next-generation sequencing technology in precision oncology. Effective personalized diagnostics requires the detection of variants with often very low frequencies. This can be achieved...

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Detalles Bibliográficos
Autores principales: Hermann, Bernd Timo, Pfeil, Sebastian, Groenke, Nicole, Schaible, Samuel, Kunze, Robert, Ris, Frédéric, Hagen, Monika Elisabeth, Bhakdi, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065719/
https://www.ncbi.nlm.nih.gov/pubmed/33808158
http://dx.doi.org/10.3390/genes12040507

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065719/
https://www.ncbi.nlm.nih.gov/pubmed/33808158
http://dx.doi.org/10.3390/genes12040507

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