Difference between revisions of "File:Fig2 Tsai JofPersMed2016 6-1.png"
Shawndouglas (talk | contribs) |
Shawndouglas (talk | contribs) (Added summary.) |
||
Line 1: | Line 1: | ||
==Summary== | |||
{{Information | |||
|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. | |||
|Source={{cite journal |journal=Journal of Personalized Medicine |title=Bioinformatics workflow for clinical whole genome sequencing at Partners HealthCare Personalized Medicine |author=Tsai, E.A.; Shakbatyan, R.; Evan, J.; Rossetti, P.; Graham, C.; Sharma, H.; Lin, C.-F., Lebo, M.S. |volume=6 |issue=1 |pages=12 |year=2016 |doi=10.3390/jpm6010012 |pmid=26927186 |pmc=PMC4810391}} | |||
|Author=Tsai, E.A.; Shakbatyan, R.; Evan, J.; Rossetti, P.; Graham, C.; Sharma, H.; Lin, C.-F., Lebo, M.S. | |||
|Date=2016 | |||
|Permission=[http://creativecommons.org/licenses/by/4.0/ Creative Commons Attribution 4.0 International] | |||
}} | |||
== Licensing == | == Licensing == | ||
{{cc-by-4.0}} | {{cc-by-4.0}} |
Latest revision as of 21:45, 21 November 2016
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. |
---|---|
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. https://www.ncbi.nlm.nih.gov/pmc/articles/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) |
|
Other versions |
Licensing
|
This work is licensed under the Creative Commons Attribution 4.0 License. |
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 21:44, 21 November 2016 | 300 × 769 (26 KB) | Shawndouglas (talk | contribs) |
You cannot overwrite this file.
File usage
The following 2 pages use this file: