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Beyond the Variants: Mutational Patterns in Next-Generation Sequencing Data for Cancer Precision Medicine
Massively parallel sequencing, also referred to as “next-generation sequencing” (NGS) provides not only information about simple, single nucleotide alterations, but it can also provide information on complex variations, such as insertions and deletions, copy number alterations, and structural varian...
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| Pubblicato in: | Front Cell Dev Biol |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7248322/ https://ncbi.nlm.nih.gov/pubmed/32509788 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.00370 |
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