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...
| Main Authors: | , , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Biomedical Informatics
2012
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524941/ |