FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-02487-5.pdf
Reference36 articles.
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4. Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–9 (2012).
5. Highnam, G. et al. An analytical framework for optimizing variant discovery from personal genomes. Nat. Commun. 6, 6275 (2015).
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