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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Front Genet
Main Authors: 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.
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2019
Teme:
Genetics
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6710408/
https://ncbi.nlm.nih.gov/pubmed/31481971
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2019.00736
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