Cargando…
iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data
BACKGROUND: Structural variations (SVs), such as insertions, deletions, inversions, and duplications, are a common feature in human genomes, and a number of studies have reported that such SVs are associated with human diseases. Although the progress of next generation sequencing (NGS) technologies...
Autores principales: | Mimori, Takahiro, Nariai, Naoki, Kojima, Kaname, Takahashi, Mamoru, Ono, Akira, Sato, Yukuto, Yamaguchi-Kabata, Yumi, Nagasaki, Masao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029547/ https://www.ncbi.nlm.nih.gov/pubmed/24564972 http://dx.doi.org/10.1186/1752-0509-7-S6-S8 |
Ejemplares similares
-
SUGAR: graphical user interface-based data refiner for high-throughput DNA sequencing
por: Sato, Yukuto, et al.
Publicado: (2014) -
Estimating copy numbers of alleles from population-scale high-throughput sequencing data
por: Mimori, Takahiro, et al.
Publicado: (2015) -
TIGAR2: sensitive and accurate estimation of transcript isoform expression with longer RNA-Seq reads
por: Nariai, Naoki, et al.
Publicado: (2014) -
HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data
por: Nariai, Naoki, et al.
Publicado: (2015) -
iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing
por: Yamaguchi-Kabata, Yumi, et al.
Publicado: (2015)