Cargando…
Construction of Whole Genomes from Scaffolds Using Single Cell Strand-Seq Data
Accurate reference genome sequences provide the foundation for modern molecular biology and genomics as the interpretation of sequence data to study evolution, gene expression, and epigenetics depends heavily on the quality of the genome assembly used for its alignment. Correctly organising sequence...
Autores principales: | Hills, Mark, Falconer, Ester, O’Neill, Kieran, Sanders, Ashley D., Howe, Kerstin, Guryev, Victor, Lansdorp, Peter M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037727/ https://www.ncbi.nlm.nih.gov/pubmed/33807210 http://dx.doi.org/10.3390/ijms22073617 |
Ejemplares similares
-
Characterizing polymorphic inversions in human genomes by single-cell sequencing
por: Sanders, Ashley D., et al.
Publicado: (2016) -
BAIT: Organizing genomes and mapping rearrangements in single cells
por: Hills, Mark, et al.
Publicado: (2013) -
Direct chromosome-length haplotyping by single-cell sequencing
por: Porubský, David, et al.
Publicado: (2016) -
InvertypeR: Bayesian inversion genotyping with Strand-seq data
por: Hanlon, Vincent C. T., et al.
Publicado: (2021) -
Genome-wide mapping of sister chromatid exchange events in single yeast cells using Strand-seq
por: Claussin, Clémence, et al.
Publicado: (2017)