Cargando…
SVA: software for annotating and visualizing sequenced human genomes
Summary: Here we present Sequence Variant Analyzer (SVA), a software tool that assigns a predicted biological function to variants identified in next-generation sequencing studies and provides a browser to visualize the variants in their genomic contexts. SVA also provides for flexible interaction w...
Autores principales: | Ge, Dongliang, Ruzzo, Elizabeth K., Shianna, Kevin V., He, Min, Pelak, Kimberly, Heinzen, Erin L., Need, Anna C., Cirulli, Elizabeth T., Maia, Jessica M., Dickson, Samuel P., Zhu, Mingfu, Singh, Abanish, Allen, Andrew S., Goldstein, David B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3129530/ https://www.ncbi.nlm.nih.gov/pubmed/21624899 http://dx.doi.org/10.1093/bioinformatics/btr317 |
Ejemplares similares
-
V-SVA: an R Shiny application for detecting and annotating hidden sources of variation in single-cell RNA-seq data
por: Lawlor, Nathan, et al.
Publicado: (2020) -
Screening the human exome: a comparison of whole genome and whole transcriptome sequencing
por: Cirulli, Elizabeth T, et al.
Publicado: (2010) -
The Characterization of Twenty Sequenced Human Genomes
por: Pelak, Kimberly, et al.
Publicado: (2010) -
ISA software suite: supporting standards-compliant experimental annotation and enabling curation at the community level
por: Rocca-Serra, Philippe, et al.
Publicado: (2010) -
Crisflash: open-source software to generate CRISPR guide RNAs against genomes annotated with individual variation
por: Jacquin, Adrien L S, et al.
Publicado: (2019)