Cargando…
SASI-Seq: sample assurance Spike-Ins, and highly differentiating 384 barcoding for Illumina sequencing
BACKGROUND: A minor but significant fraction of samples subjected to next-generation sequencing methods are either mixed-up or cross-contaminated. These events can lead to false or inconclusive results. We have therefore developed SASI-Seq; a process whereby a set of uniquely barcoded DNA fragments...
Autores principales: | Quail, Michael A, Smith, Miriam, Jackson, David, Leonard, Steven, Skelly, Thomas, Swerdlow, Harold P, Gu, Yong, Ellis, Peter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008303/ https://www.ncbi.nlm.nih.gov/pubmed/24507442 http://dx.doi.org/10.1186/1471-2164-15-110 |
Ejemplares similares
-
Optimizing illumina next-generation sequencing library preparation for extremely at-biased genomes
por: Oyola, Samuel O, et al.
Publicado: (2012) -
A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers
por: Quail, Michael A, et al.
Publicado: (2012) -
Reproducibility of Illumina platform deep sequencing errors allows accurate determination of DNA barcodes in cells
por: Beltman, Joost B., et al.
Publicado: (2016) -
Comparative performance of the BGISEQ-500 and Illumina HiSeq4000 sequencing platforms for transcriptome analysis in plants
por: Zhu, Fu-Yuan, et al.
Publicado: (2018) -
Guidelines for whole genome bisulphite sequencing of intact and FFPET DNA on the Illumina HiSeq X Ten
por: Nair, Shalima S., et al.
Publicado: (2018)