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Comparative assessments of indel annotations in healthy and cancer genomes with next-generation sequencing data
BACKGROUND: Insertion and deletion (indel) is one of the major variation types in human genomes. Accurate annotation of indels is of paramount importance in genetic variation analysis and investigation of their roles in human diseases. Previous studies revealed a high number of false positives from...
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| Vydáno v: | BMC Med Genomics |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7653722/ https://ncbi.nlm.nih.gov/pubmed/33167946 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-020-00818-6 |
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