Author:
Ruark Elise,Münz Márton,Clarke Matthew,Renwick Anthony,Ramsay Emma,Elliott Anna,Seal Sheila,Lunter Gerton,Rahman Nazneen
Publisher
Springer Science and Business Media LLC
Reference16 articles.
1. Lelieveld, S. H., Veltman, J. A. & Gilissen, C. Novel bioinformatic developments for exome sequencing. Hum Genet, 10.1007/s00439-016-1658-6 (2016).
2. Van der Auwera, G. A. et al. From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline. Curr Protoc Bioinformatics 43, 11.10.11-33, 10.1002/0471250953.bi1110s43 (2013).
3. Li, H. & Durbin, R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25, 1754–1760, 10.1093/bioinformatics/btp324 (2009).
4. Lunter, G. & Goodson, M. Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads. Genome Res 21, 936–939, 10.1101/gr.111120.110 (2011).
5. MacArthur, J. A. et al. Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants. Nucleic Acids Res 42, D873–D878, 10.1093/nar/gkt1198 (2014).
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