Items in PURPLE and links are the things you must modify. Change PURPLE items to BLACK when you save your page.
FASTQ_SHRINKER (USER MANUAL UNDER DEVELOPMENT)
FASTQ_SHRINKER
Community rating: ?????
Quality filtering, trimming and collapsing workflow to pre-process reads for genome resequencing.
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- To use FASTQ_SHRINKER, import your data in ___ format.
- Resources: http://replace.with.URL.for.tool.documentation.from.the.tool.source.org
Test Data
Info |
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Test data for this app appears directly in the Discovery Environment in the Data window under Community Data -> iplantcollaborative -> example_data -> directory. |
Input File(s)
Use TerriblyIncomprehensible.txt and HorriblyWritten.txt from the directory above as test input.
Parameters Used in App
When the app is run in the Discovery Environment, use the following parameters with the above input file(s) to get the output provided in the next section below.
Use either the "Default parameters..." section OR fill in the "Use these parameters..." section. Delete the unused section and the OR. Then, delete this note.
- Default parameters only, no further configuration needed.
OR
- Use these parameters within the DE app interface:
- parameter name - value/setting
- parameter name - value/setting
Output File(s)
Expect a text file named after the input files as output. For the test case, the output file you will find in the example_data directory is named BeautifulProse.txt.
Tool Source for App
- http://replace.with.URL.for.tool.orgfastq format.
- Fastq shrinker is a Discovery Environment workflow, a series of apps brought together to successive trimming functions and finally to remove duplicate reads from a fastq file. Potentially a useful way to prepare for assembly.