טוען...
Identification of single nucleotide variants using position-specific error estimation in deep sequencing data
BACKGROUND: Targeted deep sequencing is a highly effective technology to identify known and novel single nucleotide variants (SNVs) with many applications in translational medicine, disease monitoring and cancer profiling. However, identification of SNVs using deep sequencing data is a challenging c...
שמור ב:
| הוצא לאור ב: | BMC Med Genomics |
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| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6679440/ https://ncbi.nlm.nih.gov/pubmed/31375105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-019-0557-9 |
| תגים: |
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