Cargando…
VarB: a variation browsing and analysis tool for variants derived from next-generation sequencing data
Summary: There is an immediate need for tools to both analyse and visualize in real-time single-nucleotide polymorphisms, insertions and deletions, and other structural variants from new sequence file formats. We have developed VarB software that can be used to visualize variant call format files in...
Autores principales: | Preston, Mark D., Manske, Magnus, Horner, Neil, Assefa, Samuel, Campino, Susana, Auburn, Sarah, Zongo, Issaka, Ouedraogo, Jean-Bosco, Nosten, Francois, Anderson, Tim, Clark, Taane G. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496337/ https://www.ncbi.nlm.nih.gov/pubmed/22976080 http://dx.doi.org/10.1093/bioinformatics/bts557 |
Ejemplares similares
-
Characterization of Within-Host Plasmodium falciparum Diversity Using Next-Generation Sequence Data
por: Auburn, Sarah, et al.
Publicado: (2012) -
SnoopCGH: software for visualizing comparative genomic hybridization data
por: Almagro-Garcia, Jacob, et al.
Publicado: (2009) -
estMOI: estimating multiplicity of infection using parasite deep sequencing data
por: Assefa, Samuel A., et al.
Publicado: (2014) -
An Effective Method to Purify Plasmodium falciparum DNA Directly from Clinical Blood Samples for Whole Genome High-Throughput Sequencing
por: Auburn, Sarah, et al.
Publicado: (2011) -
Chemsearch: collaborative compound libraries with structure-aware browsing
por: Gaffney, Stephen G, et al.
Publicado: (2021)