Resources: Documentation

Extraction of ultra-high molecular weight (uHMW) gDNA - Reliably generate and sequence ultra-long read length N50s (>50 kb) - High yield - Compatible with R10.4.1 flow cells For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

For Research Use Only This is a registration-based Early Access product.

Single-cell transcriptomics method: - Requires cDNA amplicons produced using the 10X Genomics GEM-X Single Cell 3' Kit (V4), Next-GEM Single Cell 3' Kit (V3.1), or the Visium Spatial Gene Expression Kit (V1) - Library preparation time ~205 minutes - High output - PCR required For Research Use Only

Shipping and Logistics

For Research Use Only

RT-PCR for detecting the SARS-CoV-2 virus

For Research Use Only

This info sheet highlights the application and advantages of chromatin conformation capture with nanopore sequencing, known as Pore-C. The restriction enzyme Pore-C (RE-Pore-C) is intended for the manipulation of cell or nuclei suspensions to capture three-dimensional interactions of DNA within chromatin. When sequenced on Oxford Nanopore Technologies sequencing platforms, Pore-C can enable native sequencing of chromatin conformation capture extracts whilst retaining DNA base modifications. The RE-Pore-C protocol has been developed using human cell line culture, although can also be used in conjunction with other sample types, including animal tissue and insects prepared following the relevant recommended Pore-C sample preparation procedure. In addition, there is a separate protocol for Plant Pore-C which differs from the RE-Pore-C protocol to accommodate plant samples. Protocols are located in the [Extraction protocols](/documentation/results?category=prepare&topic=extraction-protocols) section of the Nanopore Community. For Research Use Only.

The effect of varying the number of PCR cycles in the PCR-cDNA Sequencing Kit

Telomere-to-telomere sequencing (T2T) know-how document

Stability of SPRI size selection beads

Short Fragment Eliminator Expansion (EXP-SFE001) know-how document

Direct-from-colony microbial sequencing: rapid Salmonella serotyping know-how and info sheet

RNA stability

RNA Integrity Number (RIN)

Equipment and consumables for the RNA Sequencing Kit family

Equipment and consumables for the Rapid Sequencing Kit family

PromethION 24/48 A-Series Technical Specification

PromethION 24/48 A-Series IT requirements

PromethION 2 Solo Technical Specification

PromethION 2 Solo IT requirements

PromethION 2 Integrated Technical Specification

PromethION 2 Integrated IT requirements

PromethION 24 A100 Technical Specification

Polyadenylation of non-poly(A) transcripts using E. coli poly(A) polymerase

Accurate poly(A) tail length estimation for Direct RNA Sequencing (SQK-RNA002) and cDNA (SQK-PCS111, SQK-PCB111.24) sequencing kits

OND GridION Mk1 Technical Specification

OND GridION Mk1 IT requirements

MinIT Technical Specification

MinION Mk1D Technical Specification

MinION Mk1D IT requirements

MinION Mk1C Technical Specification

MinION Mk1B Technical Specification

MinION Mk1B IT requirements

MinION Mk1C IT requirements

Equipment and consumables for the Ligation Sequencing Kit family

Ligation Sequencing sample input and flow cell loading know-how

DNA library stability - Ligation Sequencing Kit (SQK-LSK109)

GridION Q technical specification

GridION Q OS build

GridION Q IT requirements

GridION Mk1 Technical Specification

GridION Mk1 IT requirements

Flow Cell Wash Kit (EXP-WSH004 or EXP-WSH004-XL) know-how

Flongle Adapter Technical Specification

Enrichment of polyadenylated RNA molecules know-how document

DNA stability - storage

DNA stability - freeze-thawing

Updated method for cell-free DNA (cfDNA) methylation profiling

Optimisation of library preparation for longer cell-free DNA (cfDNA) libraries

Assessment of cfDNA extraction kits for nanopore sequencing

Comparative analysis of cfDNA collection tubes for nanopore sequencing

Cell storage

Blood storage

Telo-Seq - info sheet and recommendations

SPRI size selection protocol for >1.5-2 kb DNA fragments

A method to remove amplified cDNA artefact in SQK-PCS111 and SQK-PCB111.24 libraries

Sequencing products of multiple displacement amplification (MDA)

Size selection of HMW DNA by semi-selective DNA precipitation

For Research Use Only

VolTRAX V2B Technical Specification

A method to remove highly abundant globin transcripts from human blood RNA samples

CRISPR-Cas9 targeted sequencing - supplementary information (Q-SQK-CS9109)

Size selection of HMW DNA using the BluePippin

Adeno-associated virus (AAV) sequencing - development notes and best practices

For Research Use Only.

The fastest and simplest protocol to sequence plasmid DNA - For multiplexing up to 96 samples - Library preparation time ~60 minutes - High yield - Fragmentation - Compatible with R10.4.1 flow cells For Research Use Only

The fastest and simplest protocol to sequence amplicon DNA - For multiplexing up to 96 single species amplicon samples - Optimised for 500 bp – 5 kb amplicons. - Library preparation time ~60 minutes - High yield - Fragmentation - Compatible with R10.4.1 flow cells For Research Use Only

The fastest and simplest protocol for genomic DNA involving: - ~10 mins library prep - Fragmentation - No third-party ligase needed - No PCR __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__ For Research Use Only

This protocol: - is a rapid method to perform metagenomic sequencing for identification of bacterial, fungal and viral pathogens. - consists of a two-in-one method that splits sample into bacterial/fungal sample preparation and viral/acellular sample preparation. - provides a recommended host depletion and extraction method for respiratory samples. - uses a shotgun approach to RT-PCR. - involves tagmentation, barcoding and PCR amplification. - is compatible with R10.4.1 flow cells. <br> For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

This protocol uses genomic DNA - For multiplexing 1-96 samples - Library preparation time ~60 minutes - High yield - Fragmentation - Compatible with R10.4.1 flow cells For Research Use Only

The fastest and simplest protocol for genomic DNA involving: - 60 mins library prep - high yield - fragmentation For Research Use Only

This protocol: - uses genomic DNA - has a low input requirement - method involves tagmentation, barcoding and PCR amplification - allows multiplexing of 1–24 samples - is compatible with R10.4.1 flow cells <br> For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

A protocol for amplifying the 16S rRNA gene from extracted gDNA. - Genus-level bacterial identification - Multiplex up to 24 different samples - Compatible with R10.4.1 flow cells only For Research Use Only

The fastest and simplest protocol for genomic DNA involving: - ~10 mins library prep - fragmentation - no third-party ligase needed __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__ For Research Use Only

Automated rapid barcoding method using the ElysION device outlining library preparation and sequencing. This protocol: * Is an automated method using the ElysION device * Uses genomic DNA * Enables multiplexing of up to 96 samples * Includes DNA fragmentation * Is optimised for high output * Is compatible with R10.4.1 flow cells <br> __For Research Use Only__ This method is user with an Early Access device. For more information about our Early Access programmes, please refer to this article on [product release phases](https://nanoporetech.com/news/news-blog-you-cant-put-label-innovation-or-can-you).

Instructions for working with MinKNOW. If using for the first time, please refer to the GridION Q user manual. For Research Use Only

Q system input DNA QC

Instructions for checking the number of active pores in your flow cells.

Q system data analysis

Q-Line sequencing software user guide

Q-Line sequencing software installation and maintenance guide

This guide will help you install, check and configure your PromethION 24, PromethION 48 or PromethION 24/48 A-Series. Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only.

This guide will help you install, check and configure your PromethION 2 Solo. Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only.

This guide will help you install, check and configure your PromethION 2 Integrated. Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only.

PromethION

This protocol uses extracted RNA samples - Includes reverse transcription and tiled PCR amplification - For multiplexing 1-96 samples - Library preparation time ~315 minutes - Fragmentation - Compatible with R10.4.1 flow cells For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

The fastest and simplest protocol for full-length cDNA sequencing - Offering highest yield - Higher yields than traditional cDNA synthesis - Splice variants and fusion transcripts - Compatible with R10.4.1 flow cells <br> For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

The fastest and simplest protocol for full-length cDNA sequencing - Offering highest yield - Higher yields than traditional cDNA synthesis - Splice variants and fusion transcripts - Multiplex up to 24 different samples - Compatible with R10.4.1 flow cells only <br> For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

For Research Use Only.

End-to-end method outlining sample extraction, library preparation, sequencing and data analysis. This protocol: * Uses genomic DNA * Enables multiplexing of 4-24 samples * Takes ~60 minutes for library preparation * Includes DNA fragmentation * Is optimised for high output * Is compatible with R10.4.1 flow cells <br> __For Research Use Only__

Barcoding of native genomic DNA libraries - Requires Q-SQK-LSK109 - no PCR used - using up to 24 barcodes, achieved through use of both Q-EXP-NBD104 and Q-EXP-NBD114; 12 individual barcodes are supplied with each product - allows analysis of native DNA For Research Use Only

For Research Use Only

MinKNOW - the MinION control software. For Research Use Only.

MinIT™ is a pre-configured, optimised solution to your IT requirements for MinION™ One MinIT runs one MinION It can be controlled by a laptop or tablet It contains high specification RAM, storage, communication interfaces and a GPU for reliable and robust sequencing experiments Linux OS and MinKNOW™ are pre-installed and primed to commence sample testing FOR RESEARCH USE ONLY

Checking the MinION™ Mk1B has been assembled, installed and set up correctly. Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only

This is an Early Access device. Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only

This user manual will enable the user of the MinION Mk1C to: - Power up and down the device - Learn the shortcuts enabled by touchscreen in the MinION Mk1C Graphical User Interface (GUI) - Use the Host Settings for system software configuration - Access the device remotely for control of MinKNOW and to transfer data on Windows, macOS and Linux computers - Access the device through SecureShell/the Terminal for data transfer and device configuration Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only

Single-cell transcriptomics method: - Requires cDNA amplicons produced using the 10X Genomics GEM-X Single Cell 5' Kit (V3) or the Next GEM Single Cell 5' Kit (V2) - Library preparation time ~135 minutes - High output - PCR required For Research Use Only

Method outlining sample extraction, library preparation, sequencing and data analysis. This protocol: * uses human cfDNA * is for singleplex sequencing * is compatible with R10.4.1 flow cells <br> __For Research Use Only__

Method outlining sample extraction, library preparation, sequencing and data analysis. This protocol: * uses human cfDNA * enables multiplexing of 12 samples * is compatible with R10.4.1 flow cells <br> __For Research Use Only__

The PCR-free protocol for full-length cDNA offers: - Higher yields than traditional cDNA synthesis - Analysis of splice variants & fusion transcripts - Compatibility with R10.4.1 flow cells For Research Use Only

This protocol uses extracted RNA samples - Includes reverse transcription and PCR amplification using two separate primer schemes for Influenza A and Influenza B - Includes quantification and normalisation steps to ensure equal distribution of barcodes for 24, 48 and 96 samples. - Compatible with R10.4.1 flow cells <br> For Research Use Only

This protocol uses genomic DNA - Very low input requirements (e.g. single cells) - Multiple displacement amplification (MDA) - Compatible with R10.4.1 flow cells <br> For Research Use Only

End-to-end method outlining sample extraction, library preparation, sequencing and data analysis. This protocol: - Uses genomic DNA extracted from human blood samples - Takes ~300 minutes for sample preparation and ~90 minutes for library preparation. - Requires no PCR - Is compatible with R10.4.1 flow cells __For Research Use Only__

Sequencing of adeno-associated virus (AAV) vectors. * Requires the Native Barcoding Kit 24 V14 (SQK-NBD114.24) * Includes no PCR steps * Uses up to 24 barcodes * Allows analysis of native DNA * Compatible with R10.4.1 flow cells For Research Use Only

This protocol uses N50 of 30 kb genomic DNA extracted from human cell lines * Sample preparation time: ~320 minutes and library preparation time: ~90 minutes * Data analysis: 1-2 hours * No PCR * Compatible with R10.4.1 flow cells For Research Use Only

This protocol uses N50 of 10 kb genomic DNA extracted from human cell lines - Sample preparation time: ~220 minutes and library preparation time: ~90 minutes - Data analysis: 1-2 hours - No PCR - Compatible with R10.4.1 flow cells For Research Use Only

This protocol uses genomic DNA - Library preparation time ~120 minutes - Fragmentation optional - No PCR required - Suitable for processing multiple samples simultaneously, or automated library preparation - Compatible with R10.4.1 flow cells For Research Use Only

Requires the PCR Barcoding Expansion (EXP-PBC001 or EXP-PBC096) with the Ligation Sequencing Kit V14 (SQK-LSK114) - This protocol barcodes gDNA or amplicons - Library preparation time ~150 minutes + PCR - High yield - Uses up to 96 barcodes - Includes PCR steps - Compatible with R10.4.1 flow cells For Research Use Only

Barcoding of native genomic DNA libraries - Requires the Native Barcoding Kit 96 V14 (SQK-NBD114.96) - PCR-free protocol - Using up to 96 barcodes - Allows analysis of native DNA - Compatible with R10.4.1 flow cells For Research Use Only

Barcoding of native genomic DNA libraries - Requires the Native Barcoding Kit 24 V14 (SQK-NBD114.24) - PCR-free protocol - Using up to 24 barcodes - Allows analysis of native DNA - Compatible with R10.4.1 flow cells For Research Use Only

For barcoding of native genomic DNA libraries - Requires the Multiplex Ligation Sequencing Kit V14 XL - No PCR required - Features 96 unique barcodes - Enables low-plex sequencing - Allows analysis of native DNA - Compatible with R10.4.1 flow cells <br> For Research Use Only

For Research Use Only.

This protocol: - requires the PCR Expansion (EXP-PCA001) with the Ligation Sequencing Kit V14 (SQK-LSK114) - uses genomic DNA, amplicons or cDNA - results in high yield - has a library preparation time ~140 minutes + PCR - includes PCR steps - is compatible with R10.4.1 flow cells For Research Use Only

This protocol uses Lambda control DNA - Library preparation time ~60 minutes - Fragmentation optional - No PCR - Compatible with R10.4.1 flow cells For Research Use Only

For barcoding genomic or amplicon DNA for nanopore sequencing. - Offering highest accuracy - Multiplexing up to 2,304 samples - Requires PCR steps - Compatible with R10.4.1 flow cells <br> For Research Use Only

This protocol uses amplicon DNA - Library preparation time ~60 minutes - Fragmentation optional - No PCR For Research Use Only

Barcoding of amplicon libraries - Requires the Native Barcoding Kit 96 V14 (SQK-NBD114.96) - Includes no PCR steps - Using up to 96 barcodes - Allows analysis of native DNA - Compatible with R10.4.1 flow cells For Research Use Only

Barcoding of amplicon libraries - Requires the Native Barcoding Kit 24 V14 (SQK-NBD114.24) - Includes no PCR steps - Using up to 24 barcodes - Allows analysis of native DNA - Compatible with R10.4.1 flow cells For Research Use Only

This protocol is for recovering DNA libraries from flow cells for continued sequencing - Compatible with both MinION and PromethION flow cells, and all DNA sequencing kits For Research Use Only

LamPORE SARS-CoV-2 with flow cell recalibration

LamPORE SARS-CoV-2 respiratory panel

LamPORE SARS-CoV-2 direct from saliva

LamPORE SARS-CoV-2 Control Experiment

LamPORE SARS-CoV-2

This protocol uses Lambda control DNA - High yield - Library preparation time ~60 minutes - Fragmentation optional - No PCR For Research Use Only

Kit 14 sequencing and duplex basecalling

For Research Use Only

End-to-end method outlining sample extraction, library preparation, sequencing and data analysis. This protocol: - Uses genomic DNA extracted from human saliva samples - Takes ~300 minutes for sample preparation and ~90 minutes for library preparation. - Requires no PCR - Is compatible with R10.4.1 flow cells __For Research Use Only__

End-to-end method outlining sample extraction, library preparation, sequencing and data analysis. This protocol: - Uses genomic DNA extracted from human buccal swab samples - Takes ~90 minutes for sample preparation and ~135 minutes for library preparation. - Requires no PCR - Is compatible with R10.4.1 flow cells __For Research Use Only__

This protocol uses genomic DNA - Library preparation time ~60 minutes - Fragmentation optional - No PCR - Only compatible with R10 Version HD Flow Cells For Research Use Only __This is an Early Access product__

For Research Use Only

We aim to walk you through the set up of your MinION Mk1B and your control sequencing experiment. Before you start sequencing your own RNA samples, we recommend that you sequence a control sample of the yeast enolase-2 transcript, which is supplied in your sequencing kit. Sequencing a control sample allows you to practise performing an end-to-end nanopore sequencing experiment, and to become familiar with the technology. The whole set up process typically takes 4 hours. Once started, the sequencing run takes 6 hours, but can be left unattended. If at any point you get stuck, look out for explainers and FAQs to help you.

We aim to walk you through the set up of your MinION Mk1B and your control sequencing experiment. Before you start sequencing your own RNA samples, we recommend that you sequence a control sample of the yeast enolase-2 transcript, which is supplied in your sequencing kit. Sequencing a control sample allows you to practise performing an end-to-end nanopore sequencing experiment and to become familiar with the technology. The whole set up process typically takes 4 hours. Once started, the sequencing run takes 6 hours, but can be left unattended. If at any point you get stuck, look out for explainers and FAQs to help you.

We aim to walk you through the set up of your MinION Mk1B and your control sequencing experiment. Before you start sequencing your own DNA samples, we recommend that you sequence a control sample of Lambda DNA, which is supplied in your sequencing kit. Sequencing a Lambda sample allows you to practise performing an end-to-end nanopore sequencing experiment, and to become familiar with the technology. The whole set up process typically takes 3 hours, but there are points where you can take a break. Once started, the sequencing run takes 6 hours, but can be left unattended. If at any point you get stuck, look out for explainers and FAQs to help you.

We aim to walk you through the set up of your MinION Mk1B and your control sequencing experiment. Before you start sequencing your own DNA samples, we recommend that you sequence a control sample of Lambda DNA, which is supplied in your sequencing kit. Sequencing a Lambda sample allows you to practise performing an end-to-end nanopore sequencing experiment, and to become familiar with the technology. The whole set up process typically takes 2 hours, but there are points where you can take a break. Once started, the sequencing run takes 6 hours, but can be left unattended. If at any point you get stuck, look out for explainers and FAQs to help you.

This document will help you to install, check and configure your GridION™. Our device FAQs are located [here](https://nanoporetech.com/support/Devices). For Research Use Only.

This document will help you to install, check and configure the GridION™ Q device. For Research Use Only

This protocol uses genomic DNA - Library preparation time ~60 minutes - Fragmentation optional - No PCR - Compatible with R10.4.1 flow cells For Research Use Only

This protocol uses genomic DNA - High yield - Library preparation time ~60 minutes - Fragmentation optional - No PCR For Research Use Only

For Research Use Only

For Research Use Only

For Research Use Only

Flongle™ has a disposable flow cell It is low cost It is small-scale It offers potential for pipette-free sample loading Interfaces with our current sequencing platforms For Research Use Only Note: This is largely a guide and is subject to change as Flongle evolves rapidly over this development period - please check this page regularly to ensure the instructions provided are correct.

Yeast RNA – TRIzol

Yeast RNA - Ambion RNAqueous™ Total RNA Isolation Kit

Yeast DNA

Yeast DNA (Community-developed)

Wheat (Triticum aestivum L) leaf DNA

Universal bead-beating gDNA extraction for Nanopore-only Microbial Isolate Sequencing Solution (NO-MISS)

Mycobacterium tuberculosis DNA

SPRI size selection protocol for >1.5-2 kb DNA fragments

Soil DNA

Size selection of HMW DNA by semi-selective DNA precipitation

Removal of short fragments with the Short Fragment Eliminator Expansion (EXP-SFE001)

Human blood cell-free DNA (cfDNA) extraction for singleplex sequencing

Salmon (Salmo salar) tissue DNA

Salmon (Salmo salar) blood DNA

Human cell line RNA

Restriction Enzyme Pore-C protocol

Rat tail DNA

Rat stool DNA – QIAGEN MagAttract HMW DNA Kit

Rat stool DNA – QIAamp PowerFecal DNA Kit

Rat stool DNA – QIAGEN Genomic-tip 20/G

Rat stool DNA – QIAGEN DNeasy Blood & Tissue Kit

Rat ear DNA

Rabbit spleen DNA

Rabbit skin DNA – QIAGEN Genomic-tip with ATL

Rabbit skin DNA – QIAGEN Genomic-tip

Rabbit muscle DNA – QIAGEN Genomic-tip

Rabbit muscle DNA – QIAGEN Genomic-tip with ATL

Rabbit lung DNA – QIAGEN Genomic-tip with ATL

Rabbit lung DNA – QIAGEN Genomic-tip

Rabbit liver DNA

Rabbit heart DNA

Rabbit fat DNA – QIAGEN Genomic-tip with ATL

Rabbit fat DNA – QIAGEN Genomic-tip

Rabbit brain DNA

Rabbit blood DNA – QIAamp DNA blood Midi kit

Rabbit blood DNA – QIAGEN Genomic-tip 500/G

Rabbit blood DNA – QIAGEN Puregene Blood Kit

Plasmid DNA

Restriction enzyme Pore-C protocol for plant samples

Fruit fly (Drosophila melanogaster) RNA

Button mushroom (Agaricus bisporus) DNA

Human blood cell-free DNA (cfDNA) extraction for multiplex sequencing

Shearing genomic DNA using MegaruptorⓇ 3

Reptile tissue DNA

Insect sample preparation for RE-Pore-C

Human saliva DNA

Alpha and beta globin mRNA depletion from total RNA extracted from human blood

Human blood RNA

Human blood cell-free DNA (cfDNA)

High output, long read sequencing from human blood

Hard to lyse organisms gDNA extraction for Nanopore-only Microbial Isolate Sequencing Solution (NO-MISS)

Gram-negative bacterial DNA

Gram-positive bacterial DNA – QIAGEN Blood and Cell Culture DNA Maxi Kit

Gram-positive bacterial DNA – QIAGEN Puregene Cell Kit

Gram-positive bacterial DNA – QIAGEN MagAttract HMW DNA Kit

Fungi gDNA extraction for Nanopore-only Microbial Isolate Sequencing Solution (NO-MISS)

Western clawed frog (Xenopus tropicalis) muscle DNA

Influenza A RNA

FFPE human cell DNA

Whole Japanese rice fish (medaka) DNA

Sarasins minnow testes DNA

Japanese rice fish (medaka) organ DNA

Sarasins minnow liver DNA

Sarasins minnow brain DNA

Fever tree (Cinchona pubescens) leaf DNA

High throughput genomic DNA shearing

Environmental water (eDNA)

Enrichment of polyadenylated molecules from a sample of total RNA by selective isolation of poly(A) tails

Enrichment of polyadenylated molecules from a sample of total RNA by depletion of background rRNA

Automated gDNA extraction from dry blood spots (FTA cards)

Fruit fly (Drosophila melanogaster) DNA

Shearing genomic DNA using the Covaris g-TUBE™

Whole genome colony PCR

Chicken spleen DNA – QIAGEN Genomic-tip 100/G

Chicken skin DNA – QIAGEN Genomic-tip 100/G

Chicken muscle DNA – QIAGEN Genomic-tip 100/G

Chicken lung DNA – QIAGEN Genomic-tip 100/G

Chicken liver DNA – QIAGEN Genomic-tip 100/G

Chicken liver DNA – QIAGEN Genomic-tip 100/G with ATL buffer

Chicken heart DNA – QIAGEN Genomic-tip 100/G

Chicken fat DNA – QIAGEN Genomic-tip 100/G

Chicken brain DNA – QIAGEN Genomic-tip 100/G

Chicken blood DNA – QIAGEN Genomic-tip 100/G

Chicken blood DNA – QIAamp DNA Blood Maxi Kit

Human cell line DNA – QIAGEN Genomic-tip

Human cell line DNA – QIAGEN Puregene Cell Kit

Worm (Caenorhabditis elegans) RNA

C. elegans sample preparation for RE-Pore-C

Worm (Caenorhabditis elegans) DNA

Bull sperm DNA

Buffy coat DNA

Extracting and preparing DNA from brain tissue for Oxford Nanopore Sequencing

Size selection of HMW DNA using the BluePippin

Whole blood sample preparation for RE-Pore-C

Bacteria gDNA extraction for Nanopore-only Microbial Isolate Sequencing Solution (NO-MISS)

Arabidopsis (Arabidopsis thaliana LEr) leaf RNA

Arabidopsis (Arabidopsis thaliana LEr) leaf DNA

Animal tissue preparation for RE-Pore-C

Agarose plug DNA

3’ polyadenylation of RNA transcripts using E. coli poly(A) polymerase (PAP)

Yeast cell culture RNA

Stool pellet gDNA

Size selection

Salmon sample gDNA

Restriction enzyme Pore-C sample preparation and extraction protocols

Rabbit skin gDNA

Rabbit muscle gDNA

Rabbit lung gDNA

Rabbit fat gDNA

Rabbit blood gDNA

Plant leaf gDNA

Optional fragmentation of gDNA

Nanopore-only Microbial Isolate Sequencing Solution (NO-MISS) associated extraction protocols

Mammalian sample gDNA

Gram-positive bacterial gDNA

Fish gDNA

Methods for enrichment of polyadenylated RNA molecules

Human cell line gDNA

Avian liver gDNA

Avian gDNA

Avian blood gDNA

Instructions for working with MinKNOW. If using for the first time, please refer to the user manual for your device. For Research Use Only

This is an Early Access device. For more information about our Early Access programmes, please refer to this article on [product release phases](https://nanoporetech.com/news/news-blog-you-cant-put-label-innovation-or-can-you).

This protocol: - Is for sequencing native RNA - Can be used with total RNA or an enriched sample (e.g. poly(A) tailed or ribo-depleted) as a starting input material - Requires no fragmentation - Takes approximately 135 minutes for library preparation - Is only compatible with RNA flow cells __For Research Use Only__

This protocol: - Is for sequencing native RNA - Can be used with total RNA or an enriched sample (e.g. poly(A) tailed or ribo-depleted) as a starting input material - Requires no fragmentation - Takes approximately 135 minutes for library preparation. - Is only compatible with RNA flow cells __This is an Early Access product.__ __For Research Use Only__

This protocol: - is for selecting RNA targets of your choice for sequencing native RNA. - uses total RNA as starting input material. - requires no fragmentation. - takes ~2 hours for library preparation. For Research Use Only __This is an Early Access product.__ __For more information about our Early Access programmes, please see this [article on product release phases.](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you)__

This protocol: - Is for a control experiment using kit-supplied RNA - Sequences native RNA - Requires no fragmentation - Takes approximately 135 minutes for library preparation - Is only compatible with RNA flow cells __For Research Use Only__

This protocol: - is a rapid method to perform sequencing and analysis of *Salmonella*. - uses *Salmonella* colonies from overnight cultures. - includes tagmentation, barcoding and PCR amplification. - enables multiplexing of 1-24 samples. - is compatible with R10.4.1 flow cells. <br> For Research Use Only __This is an Early Access product__ __For more information about our Early Access programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).__

Data analysis

Chemistry Technical Document

Analysis of cell-free (cf)DNA can be used for a range of uses, including cancer detection and tissue-of-origin analysis. This document is a repository for all of our internally developed methods, know-how documents and information. This will ensure our users can easily access all the required information and our recommended best practices using nanopore sequencing technology for cfDNA.

Automated end-to-end method using the ElysION device outlining sample extraction, library preparation, sequencing and analysis. This protocol: * Is an automated method using the ElysION device * Uses bacterial or fungi cells * Enables multiplexing of up to 24 samples * Includes DNA fragmentation * Is optimised for high output * Is compatible with R10.4.1 flow cells <br> __For Research Use Only__ This method is used with an Early Access device. For more information about our Early Access programmes, please refer to this article on [product release phases](https://nanoporetech.com/news/news-blog-you-cant-put-label-innovation-or-can-you).

This protocol uses genomic DNA - Hands-on setup time ~30 minutes - Automated run time ~2 hours 40 minutes - Throughput: Process 8–96 samples for singleplex library loading - Compatible with R10.4.1 Flow Cells For Research Use Only

This protocol uses genomic DNA - Automation of library preparation - Increased reproducibility and speed - Reduces human error - High sequencing output - Library preparation time ~1.5 hours hands-on-time and ~3-4 hours automation time - Fragmentation is optional - No PCR required - Multiple samples can be prepared simultaneously - Compatible with R10.4.1 flow cells For Research Use Only

This protocol uses amplicons - High yield - Library preparation time ~50 minutes - DNA ligase-free - Multiplexes up to 24 samples For Research Use Only This is a Developer Release product. For more information about our Developer Release programmes, please see [this article on product release phases](https://nanoporetech.com/about-us/news/blog-you-cant-put-label-innovation-or-can-you).

Adaptive sampling

UBikwibopsy™ (UBik) is a tool-less sample delivery device It enables anyone, anywhere to generate DNA sequence data It is aimed at the non-skilled user Sample input can be saliva, blood, urine or other biological or environmental liquid FOR RESEARCH USE ONLY