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Anaconda: AN automated pipeline for somatic COpy Number variation Detection and Annotation from tumor exome sequencing data
BACKGROUND: Copy number variations (CNVs) are the main genetic structural variations in cancer genome. Detecting CNVs in genetic exome region is efficient and cost-effective in identifying cancer associated genes. Many tools had been developed accordingly and yet these tools lack of reliability beca...
שמור ב:
| הוצא לאור ב: | BMC Bioinformatics |
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| Main Authors: | , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5627484/ https://ncbi.nlm.nih.gov/pubmed/28974218 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-017-1833-3 |
| תגים: |
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