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A novel use of random priming-based single-strand library preparation for whole genome sequencing of formalin-fixed paraffin-embedded tissue samples
The desire to analyse limited amounts of biological material, historic samples and rare cell populations has collectively driven the need for efficient methods for whole genome sequencing (WGS) of limited amounts of poor quality DNA. Most protocols are designed to recover double-stranded DNA (dsDNA)...
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Publicat a: | NAR Genom Bioinform |
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Autors principals: | , , , , , , |
Format: | Artigo |
Idioma: | Inglês |
Publicat: |
Oxford University Press
2019
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Matèries: | |
Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6919645/ https://ncbi.nlm.nih.gov/pubmed/31867579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nargab/lqz017 |
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