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Diff-seq: A high throughput sequencing-based mismatch detection assay for DNA variant enrichment and discovery
Much of the within species genetic variation is in the form of single nucleotide polymorphisms (SNPs), typically detected by whole genome sequencing (WGS) or microarray-based technologies. However, WGS produces mostly uninformative reads that perfectly match the reference, while microarrays require...
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| Publicado no: | Nucleic Acids Res |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5909455/ https://ncbi.nlm.nih.gov/pubmed/29361139 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gky022 |
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