Načítá se...
Identification of indels in next-generation sequencing data
BACKGROUND: The discovery and mapping of genomic variants is an essential step in most analysis done using sequencing reads. There are a number of mature software packages and associated pipelines that can identify single nucleotide polymorphisms (SNPs) with a high degree of concordance. However, th...
Uloženo v:
| Vydáno v: | BMC Bioinformatics |
|---|---|
| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2015
|
| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4339746/ https://ncbi.nlm.nih.gov/pubmed/25879703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0483-6 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|