Cargando…
Deep resequencing reveals excess rare recent variants consistent with explosive population growth
Accurately determining the distribution of rare variants is an important goal of human genetics, but resequencing of a sample large enough for this purpose has been unfeasible until now. Here, we applied Sanger sequencing of genomic PCR amplicons to resequence the diabetes-associated genes KCNJ11 an...
Autores principales: | Coventry, Alex, Bull-Otterson, Lara M., Liu, Xiaoming, Clark, Andrew G., Maxwell, Taylor J., Crosby, Jacy, Hixson, James E., Rea, Thomas J., Muzny, Donna M., Lewis, Lora R., Wheeler, David A., Sabo, Aniko, Lusk, Christine, Weiss, Kenneth G., Akbar, Humeira, Cree, Andrew, Hawes, Alicia C., Newsham, Irene, Varghese, Robin T., Villasana, Donna, Gross, Shannon, Joshi, Vandita, Santibanez, Jireh, Morgan, Margaret, Chang, Kyle, IV, Walker Hale, Templeton, Alan R., Boerwinkle, Eric, Gibbs, Richard, Sing, Charles F. |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060603/ https://www.ncbi.nlm.nih.gov/pubmed/21119644 http://dx.doi.org/10.1038/ncomms1130 |
Ejemplares similares
-
Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders
por: Schaaf, Christian P., et al.
Publicado: (2011) -
Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia
por: Sheehan, Vivien A., et al.
Publicado: (2014) -
Community‐based recruitment and exome sequencing indicates high diagnostic yield in adults with intellectual disability
por: Sabo, Aniko, et al.
Publicado: (2020) -
Genetic diversity in India and the inference of Eurasian population expansion
por: Xing, Jinchuan, et al.
Publicado: (2010) -
MAGERI: Computational pipeline for molecular-barcoded targeted resequencing
por: Shugay, Mikhail, et al.
Publicado: (2017)