Cargando…
Digital PCR provides sensitive and absolute calibration for high throughput sequencing
BACKGROUND: Next-generation DNA sequencing on the 454, Solexa, and SOLiD platforms requires absolute calibration of the number of molecules to be sequenced. This requirement has two unfavorable consequences. First, large amounts of sample-typically micrograms-are needed for library preparation, ther...
Autores principales: | White, Richard A, Blainey, Paul C, Fan, H Christina, Quake, Stephen R |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2667538/ https://www.ncbi.nlm.nih.gov/pubmed/19298667 http://dx.doi.org/10.1186/1471-2164-10-116 |
Ejemplares similares
-
Correction: Digital PCR provides sensitive and absolute calibration for high throughput sequencing
por: White, Richard A, et al.
Publicado: (2009) -
A Bayesian method for calculating real-time quantitative PCR calibration curves using absolute plasmid DNA standards
por: Sivaganesan, Mano, et al.
Publicado: (2008) -
A quantitative PCR method for measuring absolute telomere length
por: O'Callaghan, Nathan J, et al.
Publicado: (2011) -
Automated degenerate PCR primer design for high-throughput sequencing improves efficiency of viral sequencing
por: Li, Kelvin, et al.
Publicado: (2012) -
Sensitive and high throughput quantification of abscisic acid based on quantitative real time immuno-PCR
por: Su, Yi, et al.
Publicado: (2018)