File:Fig2 Tsai JofPersMed2016 6-1.png

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Summary
| Description | 
 Figure 2. Bioinformatics Workflow. Our process is divided into four major phases. During this process, there are three trigger points that require manual hands-on time: (1) Alignment and Variant Calling; (2) Annotation and Upload to Oracle SQL; and (3) Variant Filtration. Segmenting these processes offer the ability to check the data integrity throughout this process and the flexibility of utilizing parts of these scripts for processing a non-standard clinical or research sample.  | 
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| Source | 
 Tsai, E.A.; Shakbatyan, R.; Evan, J.; Rossetti, P.; Graham, C.; Sharma, H.; Lin, C.-F., Lebo, M.S. (2016). "Bioinformatics workflow for clinical whole genome sequencing at Partners HealthCare Personalized Medicine". Journal of Personalized Medicine 6 (1): 12. doi:10.3390/jpm6010012. PMC PMC4810391. PMID 26927186. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=PMC4810391.  | 
| Date | 
 2016  | 
| Author | 
 Tsai, E.A.; Shakbatyan, R.; Evan, J.; Rossetti, P.; Graham, C.; Sharma, H.; Lin, C.-F., Lebo, M.S.  | 
| Permission (Reusing this file)  | 
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Licensing
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This work is licensed under the Creative Commons Attribution 4.0 License. | 
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| current | 21:44, 21 November 2016 | 300 × 769 (26 KB) | Shawndouglas (talk | contribs) | 
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