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Ligation Sequencing Kit features
This kit is recommended for users who:
- want to optimise their sequencing experiment for throughput
- would like to utilise upstream processes such as size selection, whole genome amplification, or enrichment for long reads
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Introduction to the low input genomic DNA protocol
This protocol describes how to carry out sequencing of genomic DNA using the Ligation Sequencing Kit (SQK-LSK110). It is highly recommended that a Lambda control experiment is completed first to become familiar with the technology.
Steps in the sequencing workflow:
Prepare for your experiment
You will need to:
- Ensure you have your sequencing kit, the correct equipment and third-party reagents
- Download the software for acquiring and analysing your data
- Check your flow cell to ensure it has enough pores for a good sequencing run
Library preparation
You will need to:
- Fragment your DNA (this step is optional)
- Amplify the DNA using the Primer Mix supplied in the PCR Expansion Pack (EXP-PCA001)
- Attach sequencing adapters supplied in the Ligation Sequencing Kit to the DNA ends
- Prime the flow cell, and load your DNA library onto the flow cell
Sequencing and analysis
You will need to:
- Start a sequencing run using the MinKNOW software, which will collect raw data from the device and convert it into basecalled reads
- Start the EPI2ME software and select a workflow for further analysis (this step is optional)