Cargando…
SInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence data
BACKGROUND: The rapid advancements in the field of genome sequencing are aiding our understanding on many biological systems. In the last five years, computational biologists and bioinformatics specialists have come up with newer, better and more efficient tools towards the discovery, analysis and i...
Autores principales: | Pattnaik, Swetansu, Gupta, Saurabh, Rao, Arjun A, Panda, Binay |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926339/ https://www.ncbi.nlm.nih.gov/pubmed/24495296 http://dx.doi.org/10.1186/1471-2105-15-40 |
Ejemplares similares
-
"GenotypeColour™": colour visualisation of SNPs and CNVs
por: Barlati, Sergio, et al.
Publicado: (2009) -
SpoTyping: fast and accurate in silico Mycobacterium spoligotyping from sequence reads
por: Xia, Eryu, et al.
Publicado: (2016) -
LSCplus: a fast solution for improving long read accuracy by short read alignment
por: Hu, Ruifeng, et al.
Publicado: (2016) -
FastProNGS: fast preprocessing of next-generation sequencing reads
por: Liu, Xiaoshuang, et al.
Publicado: (2019) -
HALC: High throughput algorithm for long read error correction
por: Bao, Ergude, et al.
Publicado: (2017)