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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Bibliografiske detaljer
Main Authors: Ramos, Rommel Thiago Jucá, Carneiro, Adriana Ribeiro, Azevedo, Vasco, Schneider, Maria Paula, Barh, Debmalya, Silva, Artur
Format: Artigo
Sprog:Inglês
Udgivet: Biomedical Informatics 2012
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Software
Online adgang: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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