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MinorityReport, software for generalized analysis of causal genetic variants
BACKGROUND: The widespread availability of next generation genome sequencing technologies has enabled a wide range of variant detection applications, especially in cancer and inborn genetic disorders. For model systems and microorganisms, the same technology may be used to discover the causative mut...
Gespeichert in:
| Veröffentlicht in: | Malar J |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
BioMed Central
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5324306/ https://ncbi.nlm.nih.gov/pubmed/28231785 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12936-017-1730-2 |
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