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ZOOM! Zillions of oligos mapped
Motivation: The next generation sequencing technologies are generating billions of short reads daily. Resequencing and personalized medicine need much faster software to map these deep sequencing reads to a reference genome, to identify SNPs or rare transcripts. Results: We present a framework for h...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2008
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2732274/ https://ncbi.nlm.nih.gov/pubmed/18684737 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btn416 |
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