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...

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Detalles Bibliográficos
Autores principales: Neininger, Kerstin, Marschall, Tobias, Helms, Volkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Research Article
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

Internet

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

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