Cargando…
Large-scale inference of the point mutational spectrum in human segmental duplications
BACKGROUND: Recent segmental duplications are relatively large (≥ 1 kb) genomic regions of high sequence identity (≥ 90%). They cover approximately 4–5% of the human genome and play important roles in gene evolution and genomic disease. The DNA sequence differences between copies of a segmental dupl...
Autores principales: | Nakken, Sigve, Rødland, Einar A, Rognes, Torbjørn, Hovig, Eivind |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2640414/ https://www.ncbi.nlm.nih.gov/pubmed/19161616 http://dx.doi.org/10.1186/1471-2164-10-43 |
Ejemplares similares
-
The disruptive positions in human G-quadruplex motifs are less polymorphic and more conserved than their neutral counterparts
por: Nakken, Sigve, et al.
Publicado: (2009) -
Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift
por: Møller, Pål, et al.
Publicado: (2019) -
Methods that remove batch effects while retaining group differences may lead to exaggerated confidence in downstream analyses
por: Nygaard, Vegard, et al.
Publicado: (2016) -
Correction: Møller, P.; et al. Causes for Frequent Pathogenic BRCA1 Variants Include Low Penetrance in Fertile Ages, Recurrent De-Novo Mutations and Genetic Drift. Cancers 2019, 11, 132
por: Møller, Pål, et al.
Publicado: (2020) -
Automated amplicon design suitable for analysis of DNA variants by melting techniques
por: Ekstrøm, Per Olaf, et al.
Publicado: (2015)