Biblio
Using GPUs for the Exact Alignment of Short-Read Genetic Sequences by Means of the Burrows-Wheeler Transform. IEEE/ACM Transactions on Computational Biology and Bioinformatics (TCBB). 9
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2012. Acceleration of short and long DNA read mapping without loss of accuracy using suffix array.. Bioinformatics. 30:3396-8.
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2014. HPG pore: an efficient and scalable framework for nanopore sequencing data.. BMC Bioinformatics. 17:107.
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2016. .
2016.
Genome Maps, a new generation genome browser.. Nucleic Acids Res. 41:W41-6.
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2013. VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing.. Nucleic Acids Res. 40:W54-8.
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2012. Concurrent and Accurate Short Read Mapping on Multicore Processors.. IEEE/ACM Trans Comput Biol Bioinform. 12:995-1007.
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2015. Multicore and Cloud-Based Solutions for Genomic Variant Analysis. Euro-Par 2012: Parallel Processing Workshops. 7640
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2013. .
2012.