Cargando…
A method for positive forensic identification of samples from extremely low-coverage sequence data
BACKGROUND: Determining whether two DNA samples originate from the same individual is difficult when the amount of retrievable DNA is limited. This is often the case for ancient, historic, and forensic samples. The most widely used approaches rely on amplification of a defined panel of multi-allelic...
Autores principales: | Vohr, Samuel H., Buen Abad Najar, Carlos Fernando, Shapiro, Beth, Green, Richard E. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4672566/ https://www.ncbi.nlm.nih.gov/pubmed/26643904 http://dx.doi.org/10.1186/s12864-015-2241-6 |
Ejemplares similares
-
Coverage-dependent bias creates the appearance of binary splicing in single cells
por: Buen Abad Najar, Carlos F, et al.
Publicado: (2020) -
Structural vs. functional mechanisms of duplicate gene loss following whole genome doubling
por: Sankoff, David, et al.
Publicado: (2015) -
Forensic identification of severely degraded Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss) tissues
por: Dalvin, Sussie, et al.
Publicado: (2010) -
BAMscale: quantification of next-generation sequencing peaks and generation of scaled coverage tracks
por: Pongor, Lorinc S., et al.
Publicado: (2020) -
PathoScope 2.0: a complete computational framework for strain identification in environmental or clinical sequencing samples
por: Hong, Changjin, et al.
Publicado: (2014)