Q-Line Direct RNA Sequencing Kit (Q-SQK-RNA004) (Q_RNA004_RevA_01Jun2026)
GridION: Protocol
Q-Line Direct RNA Sequencing Kit (Q-SQK-RNA004) V Q_RNA004_RevA_01Jun2026
For Research Use Only. Not for use in diagnostic procedures.
Manufacturer: Oxford Nanopore Technologies, Gosling Building, Edmund Halley Rd, Oxford Science Park, Oxford, OX4 4DQ, United Kingdom
FOR RESEARCH USE ONLY.
NOT FOR USE IN DIAGNOSTIC PROCEDURES.
Contents
Introduction to the protocol
Library preparation
概览
For Research Use Only. Not for use in diagnostic procedures.
Manufacturer: Oxford Nanopore Technologies, Gosling Building, Edmund Halley Rd, Oxford Science Park, Oxford, OX4 4DQ, United Kingdom
1. Overview of the protocol
This kit is recommended for users who:
- Want to sequence native RNA
- Want to use total RNA or an enriched (e.g. poly(A)-tailed) sample as a starting input material
This protocol describes how to carry out sequencing of native RNA using the Q-Line Direct RNA Sequencing Kit (Q-SQK-RNA004). Starting from either poly(A)-tailed RNA or total RNA, a second complementary cDNA strand is synthesised for stability by reverse transcription. Sequencing adapters are then attached to the RNA-cDNA hybrid for sequencing on the Q-Line MinION Flow Cell RNA (Q-FLO-MIN004R). This kit requires no fragmentation and provides enough material for six reactions.
Note: The complementary cDNA strand is not sequenced, but improves the RNA sequencing output.
Workflow
Reverse transcription adapters are annealed to the poly(A) tails of full-length RNA, followed by synthesis of the complementary strand by reverse transcription. Sequencing adapters are then ligated to the RNA–cDNA hybrid ends, and the prepared library is loaded onto a flow cell for sequencing.
Steps in the sequencing workflow:
Prepare for your experiment
Note: We recommend following RNA handling guidelines and Good Laboratory Practice when carrying out this protocol to prevent degradation of the RNA substrate. Key practices include wearing PPE and changing gloves frequently, decontaminating work surfaces and equipment, using clean nuclease-free consumables/reagents and keeping samples on ice.
You will need to:
- Extract your RNA, and check its length, quantity, and purity.
- Ensure you have a Q-Line Direct RNA Sequencing Kit (Q-SQK-RNA004), the correct equipment and third-party reagents.
- Check your flow cell(s) to ensure they have sufficient health to run the assay. A failed flow cell check will prevent the start of a run.
Library preparation
You will need to:
- Synthesise the complementary strand of the RNA.
- Attach sequencing adapters to the ends of the RNA–cDNA hybrid.
- Prime the flow cell, and load your RNA library onto the flow cell.
Sequencing and analysis
You will need to:
- Start a sequencing run using the Sequencing Software, which will collect raw data from the device and basecall the reads.
Unlike DNA, RNA is translocated through the nanopore in the 3'–5' direction. However, the basecalling algorithms automatically flip the data, and the reads are displayed 5'–3'.
Compatibility of this protocol
This protocol should only be used in combination with:
- Q-Line Direct RNA Sequencing Kit (Q-SQK-RNA004)
- Q-Line GridION
- Q-Line MinION Flow Cell RNA (Q-FLO-MIN004R)
Considerations for use
Warnings
- Follow Good Laboratory Practice in relation to personal safety, including but not limited to the use of personal protective equipment when handling the samples and test reagents. Refer to Safety Data Sheets provided with the product for specific safety requirements.
- Take care to prevent the reagents from contacting your skin, eyes, and mucous membranes.
- If contact occurs, immediately wash the affected area with soap and water. Thoroughly wash hands after handling samples and test reagents.
- In the event of a serious incident, contact the Manufacturer of the device. The user may also wish to contact the competent authority of the Member State in which the device was used.
- The Q-Line GridION as supplied provides only raw sequence data, which requires validated downstream analysis and the inclusion of assay-specific controls.
- Using the Q-Line GridION outside of the intended use is not recommended and is at the user’s risk.
Precautions
- Refer to local or WHO health and safety guidance for handling samples containing hazard group (HG)/BioSafety Level (BSL) 3 organisms.
- Decontaminate surfaces with 0.5% sodium hypochlorite (bleach) diluted with deionised or purified water.
- Prevent contamination of reagents by following standard contamination prevention procedures including but not limited to the use of personal protective equipment and using filter pipette tips for handling nucleic acids.
- Reagents must be stored under the indicated storage conditions before and after use.
- Waste should be disposed of in accordance with local waste disposal regulations.
- Do not mix different lots of reagents.
- We recommend using DNase-free pipette tips.
- Never reuse the consumables intended for single use (for example, tips, gloves, and test tubes).
- When using a pipette, use correct volumes and adhere to manufacturer’s instructions. The use of multichannel pipettes is recommended where possible. Mouth pipettes must not be used.
- Do not use the reagents if the package is damaged or reagent tubes are leaking (reagents may be compromised, leading to an incorrect result). Please contact technical support.
- Do not use test reagents after their expiration date.
- Do not use the flow cell if the package is damaged or the flow cell is leaking as the flow cell may be compromised, leading to an incorrect result. If leakage occurs, refer to the Flow Cell Safety Data Sheet for handling guidance, and contact technical support.
- After use, the flow cell must be prepared for return and disposal as described in the Q-Line GridION user guide.
Sequencing performance specifications
| Library description | Sequencing run time | Accuracy | Output |
|---|---|---|---|
| Poly(A)-tailed RNA (RCS) | 24 hours | ~98.1% modal single-read accuracy | >2.6 x106 reads |
| QPCR human reference total RNA | 24 hours | ~97.4% modal single-read accuracy | >2.0 x106 reads |
Statistics are representative of average observed performance in verification tests. Values vary depending on sample quality, library preparation method, flow cell type, and basecalling model. Values provided assume high-quality samples that are prepared following our optimised protocols.
2. Equipment and consumables
材料
- 8 μl总量为300 ng的带PolyA尾RNA 或8 μl总量为1 µg的总RNA
- 直接RNA测序试剂盒(SQK-RNA004)
耗材
- Q-Line MinION Flow Cell RNA (Q-FLO-MIN004R)
- 供 Oxford Nanopore Technologies® 直接 RNA 测序使用的 NEBNext® 配套模块(E3440)
- Agencourt RNAClean XP 磁珠 (Beckman Coulter®,A63987)
- 新制备的70%乙醇(用无核酸酶水配制)
- 0.2 ml 薄壁PCR管
- 1.5 ml Eppendorf DNA LoBind 离心管
- Qubit™ RNA HS Assay(RNA 高灵敏度检测)试剂盒(ThermoFisher,Q32852)
- Qubit™ dsDNA HS Assay(双链 DNA 高灵敏度检测)试剂盒(ThermoFisher,Q32851)
- Qubit™ 分析管(Invitrogen, Q32856)
仪器
- Q-Line GridION (Q-GRD-MK1)
- Q-Line MinION Flow Cell Light Shield
- 迷你离心机
- 计时器
- 热循环仪
- 适用于 1.5ml Eppendorf 离心管的磁性分离架
- Hula混匀仪(低速旋转式混匀仪)
- 涡旋混匀仪
- 盛有冰的冰桶
- Qubit™ 荧光计(或用于质控检测的等效仪器)
- Eppendorf 5424 离心机(或等效器材)
- P1000 移液枪和枪头
- P200 移液枪和枪头
- P100 移液枪和枪头
- P20 移液枪和枪头
- P10 移液枪和枪头
- P2 移液枪和枪头
Input RNA
It is important that the input RNA meets the quantity and quality requirements. Using too little or too much RNA, or RNA of poor quality (e.g. fragmented or containing chemical contaminants) can affect your library preparation.
For instructions on how to perform quality control of your RNA sample, please read the Input DNA/RNA QC protocol.
供 Oxford Nanopore Technologies® 直接 RNA 测序使用的 NEBNext® 配套模块
我们建议您购买 供 Oxford Nanopore Technologies® 直接 RNA 测序使用的 NEBNext® 配套模块(E3440)。该配套模块内包含所有与直接 RNA 测序试剂盒配套使用的 NEB 试剂。
您亦可从 NEB 单独采购配套模块中包含的试剂。
Q-Line Direct RNA Sequencing Kit (Q-SQK-RNA004) contents
| Name | Abbreviation | Cap colour | Quantity | Minimum fill volume per container (µl) |
|---|---|---|---|---|
| RT Adapter | RTA | Blue | 1 | 6 |
| RNA Ligation Adapter | RLA | Green | 1 | 36 |
| Wash Buffer | WSB | Orange | 2 | 900 |
| RNA Elution Buffer | REB | Amber | 1 | 78 |
| Library Solution | LIS | White cap with pink label | 1 | 153 |
| Sequencing Buffer | SB | Red | 1 | 225 |
| RNA Flush Tether | RFT | Violet | 1 | 180 |
| Flow Cell Flush | FCF | N/A | 1 | 7,020 |
3. Computer requirements and software
Q-Line GridION IT requirements
The Q-Line GridION device contains all the hardware required to control up to five sequencing experiments simultaneously and acquire the data. The device is further enhanced with high-performance GPU technology for real-time basecalling. Read more in the Q-Line GridION configuration guide.
The Sequencing Software
The Sequencing Software controls the Q-Line GridION, collects sequencing data in real-time and processes it into basecalled reads. The software can also demultiplex reads by barcode, and basecall/demultiplex data after a sequencing run has completed. You will be using the Sequencing Software for every assay you run.
For instructions on how to run the Sequencing Software on the Q-Line GridION, please refer to the Q-Line GridION user guide.
4. Flow cell check
Once an RNA library has been prepared using this protocol, we do not recommend storing it; the library should be sequenced immediately. Therefore, a flow cell check is recommended before starting library preparation.
Note: This protocol describes the process of starting a sequencing run using the default Q-SQK-RNA004 assay supplied with Q-Line GridION. For more information on setting up a sequencing run, see the Q-Line GridION user guide. For more information on configuring an assay definition file for your own assay, see the Q-Line GridION configuration guide. Ensure you select the correct assay for your experiment.
Slide open the Q-Line GridION lid.
Insert the Q-Line MinION Flow Cell.
Insert the flow cell into the device under the clip.
Press down firmly to ensure correct thermal and electrical contact.
Open the Sequencing Software and navigate to the Run setup page.
Select the Q-SQK-RNA004 assay and click Continue.
Import and/or select the correct sample sheet for your sequencing assay run, and then click Continue.

For instructions on how to prepare and import a sample sheet, please refer to the Q-Line GridION user guide.
Run a flow cell check.

Ensure the flow cell has passed the flow cell check before proceeding.
If a flow cell fails the flow cell check, remove and reinsert the flow cell before running the flow cell check again.
If a flow cell fails a second flow cell check, replace the flow cell.
5. Library preparation
材料
- 8 μl总量为300 ng的带PolyA尾RNA 或8 μl总量为1 µg的总RNA
- 逆转录接头(RTA)
- 清洗缓冲液(WSB)
- RNA连接接头(RLA)
- RNA洗脱缓冲液(REB)
耗材
- Agencourt RNAClean XP 磁珠 (Beckman Coulter®,A63987)
- NEBNext® 配套模块(NEB,E3440S)中的 Induro® 逆转录酶 和 5x Induro® 逆转录反应缓冲液
- NEBNext® 配套模块(NEB,E3440S)中的 10mM 脱氧核糖核苷三磷酸(dNTP)溶液
- NEBNext® 配套模块(NEB,E3440S)中的 NEBNext® 快速连接反应缓冲液
- NEBNext® 配套模块(NEB,E3440S)中的 2M U/ml T4 DNA 连接酶
- NEBNext® 配套模块(NEB,E3440S)中的小鼠 RNase 抑制剂
- NEBNext® 配套模块(NEB,E3440S)中的无核酸酶水
- 新制备的70%乙醇(用无核酸酶水配制)
- 0.2 ml 薄壁PCR管
- 1.5 ml Eppendorf DNA LoBind 离心管
- Qubit™ RNA HS Assay(RNA 高灵敏度检测)试剂盒(ThermoFisher,Q32852)
- Qubit™ dsDNA HS Assay (双链 DNA 高灵敏度检测)试剂盒(ThermoFisher,Q32851)
- Qubit™ 分析管(Invitrogen, Q32856)
仪器
- 涡旋混匀仪
- 迷你离心机
- 热循环仪
- Hula混匀仪(低速旋转式混匀仪)
- 磁性分离架
- Qubit™ 荧光计(或用于质控检测的等效仪器)
- 盛有冰的冰桶
- P1000 移液枪和枪头
- P200 移液枪和枪头
- P100 移液枪和枪头
- P20 移液枪和枪头
- P10 移液枪和枪头
- P2 移液枪和枪头
- Eppendorf 5424 离心机(或等效器材)
Perform a flow cell check
We recommend performing a flow cell check before starting your library preparation.
Thaw all reagents at room temperature, briefly spin down and mix each reagent using the appropriate method shown in the table below, and then store on ice:
| Reagent | 1. Thaw at room temperature | 2. Briefly spin down | 3. Mix well by pipetting or vortexing |
|---|---|---|---|
| RT Adapter (RTA) | ✓ | ✓ | Pipette |
| NEBNext® Quick Ligation Reaction Buffer* | ✓ | ✓ | Vortex |
| T4 DNA Ligase 2M U/ml | Not frozen | ✓ | Pipette |
| Murine RNase Inhibitor | ✓ | ✓ | Pipette |
| Induro® Reverse Transcriptase | Not frozen | ✓ | Pipette |
| 5x Induro® RT Reaction Buffer | ✓ | ✓ | Vortex |
| 10 mM dNTP solution | ✓ | ✓ | Vortex |
| Agencourt RNAClean XP beads | Not frozen | Not required | Vortex |
| RNA Ligation Adapter (RLA) | ✓ | ✓ | Pipette |
| Wash Buffer (WSB) | ✓ | ✓ | Vortex |
| RNA Elution Buffer (REB) | ✓ | ✓ | Vortex |
*The NEBNext Quick Ligation Reaction Buffer may have a little precipitate. Allow the buffer to come to room temperature and then pipette the buffer up and down several times to break up the precipitate, followed by vortexing the tube for several seconds to ensure the reagent is thoroughly mixed.
Prepare the RNA in nuclease-free water as follows:
- Transfer 300 ng of poly(A)-tailed RNA or 1 µg of total RNA into a 0.2 ml thin-walled PCR tube.
- Adjust the volume to 8.5 µl with nuclease-free water.
- Mix thoroughly by flicking the tube to avoid unwanted shearing.
- Spin down briefly in a microfuge.
In the 0.2 ml thin-walled PCR tube containing your RNA sample, combine the reagents in the following order:
| Reagent | Volume |
|---|---|
| RNA sample | 8.5 µl |
| NEBNext Quick Ligation Reaction Buffer | 3 µl |
| Murine RNase Inhibitor | 1 µl |
| RT Adapter (RTA) | 1 µl |
| T4 DNA Ligase | 1.5 µl |
| Total | 15 µl |
Mix by pipetting, then briefly spin down.
Incubate the reaction for 10 minutes at room temperature.
In a clean 1.5 ml Eppendorf DNA LoBind tube, combine the following reagents to prepare the reverse transcription mix:
| Reagent | Volume |
|---|---|
| Nuclease-free water | 13 µl |
| 10 mM dNTPs | 2 µl |
| 5x Induro RT reaction buffer | 8 µl |
| Total | 23 µl |
Transfer the reverse transcription mix to the 0.2 ml PCR tube containing your RT Adapter-ligated RNA and mix by pipetting.
Add 2 µl of Induro Reverse Transcriptase to the reaction and mix by pipetting.
Briefly spin down the sample.
Place the tube in a thermal cycler and incubate at 60°C for 30 minutes, then 70°C for 10 minutes with a lid temperature of 110°C. Cool the sample to 4°C and briefly spin down before proceeding to the next step.
Transfer the sample to a clean 1.5 ml Eppendorf DNA LoBind tube.
Resuspend the stock of Agencourt RNAClean XP beads by vortexing.
Add 72 µl of resuspended Agencourt RNAClean XP beads to the reverse-transcribed reaction and mix by pipetting.
Incubate on a hula mixer (rotator mixer) for 5 minutes at room temperature.
During this incubation, freshly prepare 200 µl of 70% ethanol in nuclease-free water. Mix by vortexing for at least 15 seconds.
When the 5-minute incubation is complete, spin down the sample and pellet on a magnetic rack.
Keep the tube on the magnetic rack and wash the beads with 150 µl of freshly prepared 70% ethanol, as described below:
- Add 150 µl of freshly prepared 70% ethanol to the tube and ensure the beads are pelleted on one side of the tube.
- Keeping the magnetic rack on the benchtop, rotate the tube by 180°. Wait for the beads to migrate towards the magnet and to form a pellet.
- Rotate the tube 180° again (back to the starting position), and wait for the beads to pellet again.
Carefully remove the 70% ethanol using the same pipette set to 150 µl and discard.
Briefly spin down and place the tube back on the magnetic rack.
Once the supernatant is clear and colourless, keep the tube on the magnetic rack and pipette off any residual ethanol. Allow to dry for 30 seconds, but do not dry the pellet to the point of cracking.
Remove the tube from the magnetic rack and resuspend the pellet in 23 µl nuclease-free water. Incubate for 5 minutes at room temperature.
Pellet the beads on the magnetic rack until the eluate is clear and colourless.
Transfer 23 µl of eluate to a clean 1.5 ml Eppendorf DNA LoBind tube.
At this stage the RT-RNA sample can be stored at –80°C for later use.
Note: This is the only pause point in this protocol.
The length of time your RT-RNA sample can be stored should be validated for your assay.
In the same 1.5 ml Eppendorf DNA LoBind tube, combine the reagents in the following order:
| Reagent | Volume |
|---|---|
| RT-RNA sample | 23 µl |
| NEBNext Quick Ligation Reaction Buffer | 8 µl |
| RNA Ligation Adapter (RLA) | 6 µl |
| T4 DNA Ligase | 3 µl |
| Total | 40 µl |
Mix by pipetting.
Incubate the reaction for 10 minutes at room temperature.
Resuspend the stock of Agencourt RNAClean XP beads by vortexing.
Add 16 µl of resuspended Agencourt RNAClean XP beads to the reaction and mix by pipetting.
Incubate on a hula mixer (rotator mixer) for 5 minutes at room temperature.
Spin down the sample and pellet the beads on a magnetic rack. Keep the tube on the magnetic rack for 5 minutes and pipette off the supernatant when clear and colourless.
Mix the Wash Buffer (WSB) by vortexing for 5–10 seconds.
Remove the tube from the magnetic rack and add 150 µl of the Wash Buffer to the beads. Close the tube lid and resuspend the beads by flicking the tube.
Spin down the sample, return the tube to the magnetic rack, and allow the beads to pellet for 5 minutes. Pipette off the supernatant when clear and colourless.
Repeat steps 32 and 33.
Spin down the tube, and place it back on the magnetic rack. Wait until the beads have pelleted, and then pipette off any remaining Wash Buffer (WSB).
Remove the tube from the magnetic rack and resuspend the pellet in 13 µl RNA Elution Buffer (REB) by gently flicking the tube.
Incubate for 10 minutes at room temperature.
After the incubation, spin down the tube and pellet the beads on the magnetic rack for 5 minutes until the eluate is clear and colourless.
Transfer 13 µl of eluate to a clean 1.5 ml Eppendorf DNA LoBind tube.
Quantify 1 µl of reverse-transcribed and adapted RNA using a Qubit™ fluorometer and the Qubit™ dsDNA HS assay.
Recovery quantities can vary between different inputs and library preparations and should be evaluated for your individual use case. However, we always recommend taking forward the full volume of RNA library for the best sequencing results.
The RNA library must be sequenced immediately and cannot be stored for later use.
6. Priming and loading
材料
- 测序缓冲液(SB)
- 文库溶液(LIS)
- RNA 冲洗系绳(RFT)
- 测序芯片冲洗液(FCF)
耗材
- Q-Line MinION Flow Cell RNA (Q-FLO-MIN004R)
- 1.5 ml Eppendorf DNA LoBind 离心管
仪器
- Q-Line GridION (Q-GRD-MK1)
- Q-Line MinION Flow Cell Light Shield
- 热循环仪
- Hula混匀仪(低速旋转式混匀仪)
- 适用于 1.5ml Eppendorf 离心管的磁性分离架
- 盛有冰的冰桶
- 迷你离心机
- 涡旋混匀仪
- P1000 移液枪和枪头
- P200 移液枪和枪头
- P100 移液枪和枪头
- P20 移液枪和枪头
- P2 移液枪和枪头
Priming and loading a flow cell
We recommend that you watch the Priming and loading a flow cell video before your first run.
Confirm that a flow cell check was completed and passed, and that it is still valid.
A successful flow cell check is required to proceed to the next step.
If a flow cell check has not already been successfully completed, or has expired, refer to the instructions in the Flow cell check section.
Thaw the Sequencing Buffer (SB), Library Solution (LIS), RNA Flush Tether (RFT), and Flow Cell Flush (FCF) at room temperature. Mix by vortexing and briefly spin down.
Click Continue on the Flow cell check page in the Sequencing Software.
Ensure the library IDs shown by the Sequencing Software match those you are about to prepare.
Prepare the flow cell priming mix in a fresh 1.5 ml Eppendorf DNA LoBind tube using the reagents shown in the table below:
| Reagent | Volume per flow cell |
|---|---|
| RNA Flush Tether (RFT) | 30 µl |
| Flow Cell Flush (FCF) | 1,170 µl |
| Total | 1,200 µl |
Slide the flow cell priming port cover clockwise to open the priming port.
Note: The priming port cover is located next to the waste channel.
Take care when drawing back buffer from the flow cell.
Do not remove more than 20–30 µl, and make sure that the array of pores is covered by buffer at all times. Introducing air bubbles into the array can irreversibly damage pores.
After opening the priming port, remove any potential air bubbles under the cover by performing the following steps:
- Set a P1000 pipette to 200 µl.
- Carefully insert the tip into the priming port, holding the pipette perpendicular to the flow cell.
- Turn the wheel until the dial shows 220–230 µl to draw back 20–30 µl, or until you can see a small volume of buffer entering the pipette tip.

Note: Visually check that there is continuous buffer from the priming port across the sensor array.
Load 800 µl of the priming mix into the flow cell via the priming port, avoiding the introduction of air bubbles.

Leave the flow cell to incubate for 5 minutes.
During this time, prepare the library for loading by combining the reagents using the volumes in the table shown below:
| Reagent | Volume per flow cell |
|---|---|
| Sequencing Buffer (SB) | 37.5 µl |
| Library Solution (LIS) | 25.5 µl |
| RNA library | 12 µl |
| Total | 75 µl |
Note: Ensure the Sequencing Buffer (SB) and Library Solution (LIS) are thoroughly mixed immediately before adding to the library.
Once the 5-minute incubation is complete, gently lift the SpotON sample port cover to make the SpotON sample port accessible.
Load 200 µl of the priming mix into the flow cell priming port (not the SpotON sample port), avoiding the introduction of air bubbles.

Note: A small volume of priming mix may be visible as a meniscus over the SpotON sample port. Take care not to allow priming mix to spill over the top of the flow cell. The liquid will wick back in through the port once pressure from the pipette is no longer applied.
Mix each prepared library gently by pipetting up and down just prior to loading.
Pay careful attention to the Sequencing Software to ensure that the correct library is loaded onto the correct flow cell.
The Sequencing Software assigns libraries (based on the sample sheet column “library_id”) to flow cells automatically. The libraries must be loaded onto the correct flow cell to ensure that data is correctly attributed to the sample.
Add 75 µl of the prepared library to the flow cell via the SpotON sample port in a dropwise fashion. Ensure each drop flows into the port before adding the next.

Gently replace the SpotON sample port cover, making sure the bung enters the SpotON port.
Close the flow cell priming port.
Attach the light shield (supplied with the flow cell).

Close the lid of the Q-Line GridION, and click Continue in the Sequencing Software.
Review the details in the Sequencing Software and, if ready, click Run assay.
Note: A small prompt will appear in the bottom right corner stating that the run has started. If you did not mean to start it, click Undo within 30 seconds, and the run will not start.
For further information
Refer to the Setting up a run section of the Q-Line GridION user guide.
For technical support
Contact Oxford Nanopore Technologies technical support at: support@nanoporetech.com
