Cargando…
The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection
With the development of High-Throughput Sequencing (HTS) thousands of human genomes have now been sequenced. Whenever different studies analyze the same genome they usually agree on the amount of single-nucleotide polymorphisms, but differ dramatically on the number of insertion and deletion variant...
| Autores principales: | , , |
|---|---|
| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2015
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4551921/ https://www.ncbi.nlm.nih.gov/pubmed/26130710 http://dx.doi.org/10.1093/nar/gkv677 |