Assembly-free genome comparison based on next-generation sequencing reads and variable length patterns

BACKGROUND: With the advent of Next-Generation Sequencing technologies (NGS), a large amount of short read data has been generated. If a reference genome is not available, the assembly of a template sequence is usually challenging because of repeats and the short length of reads. When NGS reads cann...

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Detalles Bibliográficos
Autores principales: Comin, Matteo, Schimd, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168702/
https://www.ncbi.nlm.nih.gov/pubmed/25252700
http://dx.doi.org/10.1186/1471-2105-15-S9-S1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168702/
https://www.ncbi.nlm.nih.gov/pubmed/25252700
http://dx.doi.org/10.1186/1471-2105-15-S9-S1

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