Cargando…
SNP and indel frequencies at transcription start sites and at canonical and alternative translation initiation sites in the human genome
Single-nucleotide polymorphisms (SNPs) are the most common form of genetic variation in humans and drive phenotypic variation. Due to evolutionary conservation, SNPs and indels (insertion and deletions) are depleted in functionally important sequence elements. Recently, population-scale sequencing e...
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2019
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461226/ https://www.ncbi.nlm.nih.gov/pubmed/30978217 http://dx.doi.org/10.1371/journal.pone.0214816 |