Publications
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Filters: Keyword is High-Throughput Nucleotide Sequencing and Author is Carroll, Andrew [Clear All Filters]
Hidden biases in germline structural variant detection. Genome Biol. 2021 ;22(1):347.
. Parliament2: Accurate structural variant calling at scale. Gigascience. 2020 ;9(12).
. Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome. Nat Biotechnol. 2019 ;37(10):1155-1162.
. A hybrid computational strategy to address WGS variant analysis in >5000 samples. BMC Bioinformatics. 2016 ;17(1):361.
. Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline. BMC Bioinformatics. 2014 ;15:30.
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