Yüklüyor......
PennCNV in whole-genome sequencing data
BACKGROUND: The use of high-throughput sequencing data has improved the results of genomic analysis due to the resolution of mapping algorithms. Although several tools for copy-number variation calling in whole genome sequencing have been published, the noisy nature of sequencing data is still a lim...
Kaydedildi:
| Yayımlandı: | BMC Bioinformatics |
|---|---|
| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2017
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5629549/ https://ncbi.nlm.nih.gov/pubmed/28984186 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1802-x |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|