Cargando…
Reference-free SNP calling: improved accuracy by preventing incorrect calls from repetitive genomic regions
BACKGROUND: Single nucleotide polymorphisms (SNPs) are the most abundant type of genetic variation in eukaryotic genomes and have recently become the marker of choice in a wide variety of ecological and evolutionary studies. The advent of next-generation sequencing (NGS) technologies has made it pos...
Autores principales: | Dou, Jinzhuang, Zhao, Xiqiang, Fu, Xiaoteng, Jiao, Wenqian, Wang, Nannan, Zhang, Lingling, Hu, Xiaoli, Wang, Shi, Bao, Zhenmin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3472322/ https://www.ncbi.nlm.nih.gov/pubmed/22682067 http://dx.doi.org/10.1186/1745-6150-7-17 |
Ejemplares similares
-
RADtyping: An Integrated Package for Accurate De Novo Codominant and Dominant RAD Genotyping in Mapping Populations
por: Fu, Xiaoteng, et al.
Publicado: (2013) -
High-Resolution Linkage and Quantitative Trait Locus Mapping Aided by Genome Survey Sequencing: Building Up An Integrative Genomic Framework for a Bivalve Mollusc
por: Jiao, Wenqian, et al.
Publicado: (2014) -
MethylRAD: a simple and scalable method for genome-wide DNA methylation profiling using methylation-dependent restriction enzymes
por: Wang, Shi, et al.
Publicado: (2015) -
Read trimming has minimal effect on bacterial SNP-calling accuracy
por: Bush, Stephen J.
Publicado: (2020) -
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data
por: Liu, Qi, et al.
Publicado: (2012)