Φορτώνει......
cnvCurator: an interactive visualization and editing tool for somatic copy number variations
BACKGROUND: One of the most important somatic aberrations, copy number variations (CNVs) in tumor genomes is believed to have a high probability of harboring oncotargets. Detection of somatic CNVs is an essential part of cancer genome sequencing analysis, but the accuracy is usually limited due to v...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | BMC Bioinformatics |
|---|---|
| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2015
|
| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4608136/ https://ncbi.nlm.nih.gov/pubmed/26472134 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0766-y |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|