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MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data
Copy number variation (CNV) is a very important phenomenon in tumor genomes and plays a significant role in tumor genesis. Accurate detection of CNVs has become a routine and necessary procedure for a deep investigation of tumor cells and diagnosis of tumor patients. Next-generation sequencing (NGS)...
שמור ב:
| הוצא לאור ב: | Front Genet |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Frontiers Media S.A.
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7243272/ https://ncbi.nlm.nih.gov/pubmed/32499814 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00434 |
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