Digital Detection of Genetic Mutations Using SPC-Sequencing
Deletion or insertion mutations lead to a frameshift that causes misalignment between wild-type and mutated allele sequences, making it difficult to identify such mutations unambiguously by using electrophoresis-based DNA sequencing. We have previously established the feasibility of an accurate DNA...
Na minha lista:
| Publicado no: | Genome Res |
|---|---|
| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2004
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC327105/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14762066/ https://ncbi.nlm.nih.govhttps://doi.org/10.1101/gr.1344104 |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|