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Discrepancy between Agilent RIN and RINᵉ values

Created by Shweta.S Shweta.S over 1 year ago | Last modified by Carlos Vargas Carlos Vargas over 1 year ago

This Information Applies To: 2100 Bioanalyzer, 4150/4200/2200 TapeStation


Issue:

Discrepancy between Agilent Bioanalyzer RNA integrity number (RIN) and Agilent TapeStation RNA integrity number equivalent (RINe) values


Resolution: 

First, please read the following application notes about RIN and RINe:   

  • Performance of the RNA ScreenTape Assays on 2200 TapeStation System
  • Performance of the RNA ScreenTape Assays on 4150 TapeStation System

As can be seen in the application notes, in general, we expect RIN and RINe to correlate well.

However, if differences in RIN and RINe are observed, we have the following recommendations:

1. Ensure that the sample preparation protocol is followed exactly as recommended for each assay. For example:

  • For Bioanalyzer RNA assays, we recommend heat denaturing the samples before adding samples onto the chip. Although heat denaturation is optional to the workflow, it is highly recommended especially when comparing to RINe.  
  • For TapeStation RNA assays, we recommend heat denaturing samples after adding sample buffer. 

Therefore, it is important to ensure the same samples heat denatured once for a Bioanalyzer run are not used for a TapeStation run. This will cause the samples to be heat denatured twice, negatively affecting the RINe value. Also, for heat denaturation, proper tools including but not limited to properly sealable consumables and PCR cyclers.  

2. Ensure that ScreenTape and Bioanalyzer assays of comparable sensitivity and specifications are used when comparing data across the two platforms.

3. Ensure samples are loaded according to the listed specifications for each Bioanalyzer kit and TapeStation ScreenTape assay, and only compare the results of the same samples.

Finally, although we expect the two to correlate well, RIN and RINe use different algorithms. RIN uses a proprietary neural network-based algorithm to assess the entire electrophoretic trace. For RINe calculation, the upper ribosomal peak is not taken into consideration. Correct assignment of the lower marker is essential for RINe calculation whereas ladder is not required. In contrast, RINe represents the relative ratio of the signal in the fast zone to the 18S peak signal. Also, given that Bioanalyzer and TapeStation are two different platforms, differences in electrophoretic patterns as well as in RIN values compared to RINe values may occur depending upon samples. In this case, setting a separate threshold or quality cut off for RIN and RINe is recommended. 

For Research use only 

PR7000-7979

 Tip 

For further information please refer to

Agilent 2100 Bioanalyzer System Maintenance and Troubleshooting Guide
Agilent Information Center > Agilent TapeStation Systems > ScreenTape Assays > Good Measurement Practices
Agilent Information Centre > Agilent TapeStation Systems > ScreenTape Assays > Troubleshooting > Troubleshooting RNA Applications
Agilent Information Centre > Agilent TapeStation Systems > ScreenTape Assays > Troubleshooting > Frequently Asked Questions

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