Correct Long Reads

This tool has been deprecated and will be retired in a future version of the software. It has been moved to the Legacy Tools (Image legacy_tools) folder under the Tools menu, and its name has "(legacy)" appended to it.

The Correct Long Reads tool was originally designed to enable the correction of error-prone long reads. Over the past years, the quality of long reads has improved dramatically, to the point where correction is no longer needed. In addition, the most common applications such as Map Long Reads to Reference and De Novo Assemble Long Reads can now handle the older error-prone reads without prior correction. Therefore, the tool will be retired.

If you have concerns about the future retirement of this tool, please contact QIAGEN Bioinformatics Support team at ts-bioinformatics@qiagen.com.

The Correct Long Reads tool enables the correction of a set of error-prone long reads by finding overlaps between the reads, and performing a consensus error correction using Racon [Vaser et al., 2017].

Note that if the aim is to create an assembly from a set of error-prone long reads it is not recommended to run Correct Long Reads prior to De Novo Assemble Long Reads. For other applications, however, it may be beneficial to correct the reads before further analysis.

To run the Correct Long Reads tool, go to:

        Tools | Legacy Tools | Correct Long Reads (legacy) (Image correct_longreads_16_h_p)

Select one or more sequence lists containing reads.

In the next dialog, set the following parameters (figure 38.1):

Image longreadcorrect_step1
Figure 38.1: Correct Long Reads parameters



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