SeqDoC: rapid SNP and mutation detection by direct comparison of DNA sequence chromatograms

BACKGROUND: This paper describes SeqDoC, a simple, web-based tool to carry out direct comparison of ABI sequence chromatograms. This allows the rapid identification of single nucleotide polymorphisms (SNPs) and point mutations without the need to install or learn more complicated analysis software....

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Detalles Bibliográficos
Autor principal: Crowe, Mark L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1156871/
https://www.ncbi.nlm.nih.gov/pubmed/15927052
http://dx.doi.org/10.1186/1471-2105-6-133

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1156871/
https://www.ncbi.nlm.nih.gov/pubmed/15927052
http://dx.doi.org/10.1186/1471-2105-6-133

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