Cargando…
Reprever: resolving low-copy duplicated sequences using template driven assembly
Genomic sequence duplication is an important mechanism for genome evolution, often resulting in large sequence variations with implications for disease progression. Although paired-end sequencing technologies are commonly used for structural variation discovery, the discovery of novel duplicated seq...
Autores principales: | Kim, Sangwoo, Medvedev, Paul, Paton, Tara A., Bafna, Vineet |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695505/ https://www.ncbi.nlm.nih.gov/pubmed/23658221 http://dx.doi.org/10.1093/nar/gkt339 |
Ejemplares similares
-
InPhaDel: integrative shotgun and proximity-ligation sequencing to phase deletions with single nucleotide polymorphisms
por: Patel, Anand, et al.
Publicado: (2016) -
Targeted de novo phasing and long-range assembly by template mutagenesis
por: Li, Siran, et al.
Publicado: (2022) -
Partial bisulfite conversion for unique template sequencing
por: Kumar, Vijay, et al.
Publicado: (2018) -
sCNAphase: using haplotype resolved read depth to genotype somatic copy number alterations from low cellularity aneuploid tumors
por: Chen, Wenhan, et al.
Publicado: (2017) -
An efficient method to assemble linear DNA templates for in vitro screening and selection systems
por: Stein, Viktor, et al.
Publicado: (2009)