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Pubudu Saneth Samarakoon

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BMC Genomics|January 15, 2016
cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing dataPubudu Saneth Samarakoon, Hanne Sørmo Sorte, Asbjørg Stray-Pedersen, et al.
BMC Genomics|August 9, 2014
Identification of copy number variants from exome sequence dataPubudu Saneth Samarakoon, Hanne Sørmo Sorte, Bjørn Evert Kristiansen, et al.
Bioinformatics Advances|May 21, 2025
Benchmarking accelerated next-generation sequencing analysis pipelinesPubudu Saneth Samarakoon, Ghislain Fournous, Lars T Hansen, et al.
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Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
BMC Genomics|January 15, 2016
cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing dataPubudu Saneth Samarakoon, Hanne Sørmo Sorte, Asbjørg Stray-Pedersen, et al.
BMC Genomics|August 9, 2014
Identification of copy number variants from exome sequence dataPubudu Saneth Samarakoon, Hanne Sørmo Sorte, Bjørn Evert Kristiansen, et al.
Bioinformatics Advances|May 21, 2025
Benchmarking accelerated next-generation sequencing analysis pipelinesPubudu Saneth Samarakoon, Ghislain Fournous, Lars T Hansen, et al.
Pageof 1