• Implementing the Twist Human Core Exome Kit on the MIRO CANVAS

    Automated NGS library preparation and hybridization capture

    Whole exome sequencing (WES) provides a unique opportunity to dive deeply into the coding regions of the genome. It plays an important role in generating data for research and, in some cases, clinical applications.1 Strong WES analyses rely on even coverage of these regions and, ultimately, on high quality capture reactions.2 Variability in coverage can be minimized by ensuring that reagents are high quality, and by automating laboratory processes that have traditionally been performed manually.3

    The Twist Human Core Exome Kit undergoes thorough quality control testing to ensure that all probes in the probe pools are present at the appropriate levels in order to limit wasted reads.4 The uniformity of these reagents reduces costs and improves coverage of reads in singleplex and 8-plex pools.4 Automating this kit on the MIRO CANVAS reduces the potential for contamination and variability. The MIRO CANVAS also provides full walk-away automation, giving users the flexibility to perform other tasks while maintaining high quality results.

    The MIRO CANVAS NGS prep system is a digital microfluidics platform that allows customized, low throughput workflow automation for complex protocols, such as NGS library preparation and hybridization capture. The system is compatible with a wide range of reagents.5 This application note describes the results that can be expected when using the Twist Human Core Exome Kit in protocols developed for the MIRO CANVAS. The resulting research use only libraries can then be sequenced using Illumina sequencing platforms.

  • Table of contents

    Whole exome sequencing (WES) provides a unique opportunity to dive deeply into the coding regions of the genome. It plays an important role in generating data for research and, in some cases, clinical applications.1 Strong WES analyses rely on even coverage of these regions and, ultimately, on high quality capture reactions.2 Variability in coverage can be minimized by ensuring that reagents are high quality, and by automating laboratory processes that have traditionally been performed manually.3

    The Twist Human Core Exome Kit undergoes thorough quality control testing to ensure that all probes in the probe pools are present at the appropriate levels in order to limit wasted reads.4 The uniformity of these reagents reduces costs and improves coverage of reads in singleplex and 8-plex pools.4 Automating this kit on the MIRO CANVAS reduces the potential for contamination and variability. The MIRO CANVAS also provides full walk-away automation, giving users the flexibility to perform other tasks while maintaining high quality results.

    The MIRO CANVAS NGS prep system is a digital microfluidics platform that allows customized, low throughput workflow automation for complex protocols, such as NGS library preparation and hybridization capture. The system is compatible with a wide range of reagents.5 This application note describes the results that can be expected when using the Twist Human Core Exome Kit in protocols developed for the MIRO CANVAS. The resulting research use only libraries can then be sequenced using Illumina sequencing platforms.

Key benefits

  • Library preparation and hybridization capture using Twist Human Core Exome kit are automated on the MIRO CANVAS.
  • These protocols have been developed using 50 ng DNA input for library prep and 1500 ng for hybridization capture.
  • Depth of coverage, quality scores and other key metrics are comparable between manually prepared libraries and those run on the MIRO CANVAS.
  • Automating library preparation and hybridization capture on the MIRO CANVAS reduces hands-on time by over 85 %.

Overview: How to implement the Twist Human Core Exome kit on the MIRO CANVAS

Experimental set-up

The fully automated Twist Universal Library Prep protocol has been tested using 50 ng of high molecular weight DNA. DNA should be quantified using the Qubit™ dsDNA Broad Range Quantification Assay or similar before starting.6 Fragmentation, end repair, adapter ligation, amplification and purification steps are all automated in this protocol. The Twist Fast Hybridization Target Enrichment protocol has been tested using single samples and 8-plex pools, and the volume of each sample library used depends on their respective concentrations.7 Minimal hands-on sample preparation is required at the beginning of this protocol, leaving most steps automated on the MIRO CANVAS, including hybridizing probes with pools, binding targets to beads, post-capture amplification and purification.

Downloads: App note for implementing the Twist Human Core Exome Kit on the MIRO CANVAS

Graphical representation of the manual and automated Twist human exom library prep workflow.
Figure 1: Experimental workflows. Both the MIRO Universal Library Prep and Twist Fast Hybridization Target Enrichment protocols are fully automated after reaction set-up.

Methods and results

Library preparation

The MIRO Universal Library Prep (Twist) protocol has been tested using 50 ng of NA12878* gDNA. Hybridization capture was then performed manually to assess the quality of the library preparation protocol alone on the MIRO CANVAS. Replicates of the libraries prepared on the MIRO CANVAS and manually (n=4, 8 in total) were sequenced on an Illumina NextSeq 500 or 550 platform, 75 Paired-End. Key metrics, such as depth of coverage and fold-80 scores, were comparable between the methods. Additionally, both methods yielded a similar percentage of duplicated reads and reads on target (Figure 2).

*NA12878 DNA was obtained from the NIGMS Human Genetic Cell Repository at the Coriell Institute for Medical Research.

Graphical representation of the sequencing data generated from manual and automated Twist library preparation. Both methods yielded in similar results.
Figure 2: Multiple metrics were used to evaluate the sequencing data generated using both manual and Twist Universal Library Prep protocols. Hybridization capture was performed manually. All samples were subsampled to 150x raw sequencing coverage(70 M reads, 5.3 GB of data per sample).

Target enrichment

The Twist Fast Hybridization Target Enrichment protocol has been tested using inputs of 1500 ng of mixed DNA for 8-plex pools (multiplex, 187.5 ng per library) and 500 ng for individual libraries (singleplex). Samples run on the MIRO CANVAS for hybridization capture previously underwent manual library preparation. Sequencing was performed using the NextSeq High Output 75PE platform. Singleplex and 8-plex pools run on the MIRO CANVAS were compared to singleplex samples that had been enriched manually. Coverage of target bases at 20x and 30x was comparable between manual and automated protocols for single samples and 8-plex pools. Fold-80 scores were also similar between methods, with median scores varying by no more than 0.02 (Figure 3).

Graphical representation of the depth of coverage and fold-80 data for manual singleplex, automated singleplex and automated 8-plex libraries.
Figure 3: There was no significant difference between manual singleplex, MIRO CANVAS singleplex, and MIRO CANVAS 8-plex coverage of targets and fold-80 scores. All samples were subsampled to 150x raw sequencing coverage (70 M reads, 5.3 GBof data per sample).

Additional sequencing was completed using 2 x 8-plex pools, one prepared manually and the other on the MIRO CANVAS. Targets covered at 30x and fold-80 scores for each pool were comparable (Table 1). Reads for these runs were assessed using the MIRO CANVAS Integrative Genomics Viewer (IGV). The IGV outputs displayed confident mapping of target genes across multiple exons from pools enriched using the MIRO CANVAS (Figure 4).

Table 1: Key metrics were comparable for 8-plex pools enriched manually and on the MIRO CANVAS. All samples were subsampled to 150x raw sequencing coverage (70 M reads, 5.3 GB of data per sample).

Key sequencing metrics shown for manual 8-plex and automated 8-plex libraries. The two data sets are comparable.
Graphical representation of the Integrative Genomics Viewer results. The outputs show confident mapping of the target genes for manual and automated library prep.
Figure 4: Representative IGV browser tracks of EGFR exons 2-10 from core exome-enriched libraries prepared manually and on the MIRO CANVAS.

Time savings

While the overall time taken between the library preparation and hybridization capture protocols does not vary significantly between manual preparation and MIRO CANVAS automation, the hands-on time is far less for the automated applications. Manual library preparation requires about 3 hours of hands-on time, while the Twist Universal Library Prep requires about 15 minutes to set up for a fully automated run of 3 hours and 20 minutes.

The Twist Fast Hybridization Target Enrichment protocol begins with several steps that cannot be automated, such as preparing pools and hybridization mix, and therefore requires about an hour of benchtop work. The steps that follow are fully automated on the MIRO CANVAS, taking about 5.5 hours to complete. This hour of hands-on time pales in comparison to the time taken by the manual protocol, which requires as much as 7.5 hours.

References

  1. Rabbani B et al. The promise of whole-exome sequencing in medical genetics. J Hum Genet 2014; 59: 5–15. https://doi.org/10.1038/ jhg.2013.114
  2. Lelieveld SH et al. Comparison of exome and genome sequencing technologies for the complete capture of protein-coding regions. Hum Mutat 2015; 36: 815-822. https://doi.org/10.1002/humu.22813
  3. Holland I and Davies JA. Automation in the life science research laboratory. Front Bioeng Biotechnol 2020; 8: 571777. https://doi.org/10.3389/fbioe.2020.571777
  4. Twist Bioscience. Human core exome kit. Available at: Human Core Exome - Twist Bioscience Accessed Feb 2022.
  5. Miroculus. New Class of Technology. Available at: https://miroculus.com/technology/. Accessed February 2022.
  6. Miroculus, Inc. Miro Universal Library Prep (Twist) Protocol. Available at: https://miroculus.com/. Accessed: Feb 2022.
  7. Miroculus, Inc. Miro Human Exome Hyb Capture (Twist) Protocol. Available at: https://miroculus.com/. Accessed: Feb 2022.

Conclusion

  • The MIRO CANVAS is an advanced digital microfluidics platform that can be used to automate library preparation and hybridization capture with the Twist Bioscience Human Core Exome Kit. Both the Twist Universal Library Prep and Twist Fast Hybridization Target Enrichment protocols are fully automated from fragmentation to elution and hybridization to elution, respectively.
  • These automated protocols yield results comparable to their manual counterparts, with the MIRO CANVAS significantly reducing hands-on time, making it a valuable tool for any laboratory.

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  • Fay Christodoulou, PhD

    Chief Scientific Officer Microfluidics

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Instruments and accessories

MIRO CANVAS, NGS prep system MIRO Cartridge MIRO Dropgloss Twist Biosciences: Twist Human Core Exome, 12 Reactions, Kit Coriell Institute for Medical Research: Genomic DNA from LCL

MIRO CANVAS, NGS prep system

A revolutionary microfluidics platform which enables full automation of NGS prep protocols.

  • Fully automated - Simple, walk-away automation for on-demand NGS sample preparation

  • Efficient - Minimize costs with up to 75 % reduction in reagent use and only 15 minutes of hands-on time

  • Flexible - Established NGS sample prep protocols for both short- and long-read sequencing platforms

Part No. M-01-0001-001-01

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MIRO Cartridge

The MIRO Cartridge is a single use consumable suitable for running library prep workflows on the MIRO CANVAS instrument (for Research Use Only)

Part No. M-02-0001-001-03

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Miro Cartridge

MIRO Dropgloss

MIRO Dropgloss is a proprietary system reagent that helps mitigate evaporation. (for Research Use Only)

Part No. M-03-0001-001-01

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Twist Biosciences: Twist Human Core Exome, 12 Reactions, Kit

The NGS Human Core Exome provides the ability to lower sequencing costs, increase sample throughput, and achieve a higher depth of coverage across target regions with uncompromising quality.

Part No. 102026

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Coriell Institute for Medical Research: Genomic DNA from LCL

Ceph/utah Pedigree 1463 International Hapmap Project - Ceph (Plate I) [utah Residents With Ancestry From Northern And Western Europe] Cytochrome P450, Subfamily Iic, Polypeptide 19; Cyp2c19 International Hapmap Project - Ceph [utah Residents With Ancestry From Northern And Western Europe] Na Custom Service Plate 01

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