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Simplifier: a web tool to eliminate redundant NGS contigs
Modern genomic sequencing technologies produce a large amount of data with reduced cost per base; however, this data consists of short reads. This reduction in the size of the reads, compared to those obtained with previous methodologies, presents new challenges, including a need for efficient algor...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Biomedical Informatics
2012
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3524941/ https://ncbi.nlm.nih.gov/pubmed/23275695 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6026/97320630008996 |
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