Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy

As reliable, efficient genome sequencing becomes ubiquitous, the need for similarly reliable and efficient variant calling becomes increasingly important. The Genome Analysis Toolkit (GATK), maintained by the Broad Institute, is currently the widely accepted standard for variant calling software. Ho...

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Detalles Bibliográficos
Autores principales: Kendig, Katherine I., Baheti, Saurabh, Bockol, Matthew A., Drucker, Travis M., Hart, Steven N., Heldenbrand, Jacob R., Hernaez, Mikel, Hudson, Matthew E., Kalmbach, Michael T., Klee, Eric W., Mattson, Nathan R., Ross, Christian A., Taschuk, Morgan, Wieben, Eric D., Wiepert, Mathieu, Wildman, Derek E., Mainzer, Liudmila S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710408/
https://www.ncbi.nlm.nih.gov/pubmed/31481971
http://dx.doi.org/10.3389/fgene.2019.00736

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710408/
https://www.ncbi.nlm.nih.gov/pubmed/31481971
http://dx.doi.org/10.3389/fgene.2019.00736

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