Using False Discovery Rates to Benchmark SNP-callers in next-generation sequencing projects
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep01512.pdf
Reference31 articles.
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4. Aird, D. et al. Analyzing and minimizing PCR amplification bias in Illumina Sequencing libraries. Genome Biol. 12, R18 (2011).
5. Sasson, A. & Michael1, T. P. Filtering error from SOLiD Output. Bioinformatics 26, 849–850 (2010).
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