Overview: How to enable the Illumina DNA PCR-Free Library Prep kit on MIRO CANVAS

Experimental set-up

The Illumina DNA PCR free library prep protocol was designed for fully automated use on MIRO CANVAS and has been tested using high quality DNA inputs within the 50-500 ng range. DNA should be quantified using a Broad-Range Qubit quantification kit (or similar) before beginning the protocol. Libraries are quantified using ssDNA Qubit Quantification kit or qPCR. Tagmentation, post-tagmentation cleanup, ligation and library cleanup steps are all automated on MIRO CANVAS (Figure 1). Downstream normalization and pooling require hands-on time. 

Downloads: App note for enabling the Illumina DNA PCR-Free Library Prep kit on the MIRO CANVAS NGS® prep system

Results

Automating the experimental workflow on MIRO CANVAS produces library yields and insert sizes that result in quality sequencing metrics. The Illumina DNA PCR-Free Prep protocol for standard input has been modified and tested using 50-500 ng NA12878 gDNA* on MIRO CANVAS. In this modified version (Table 1), combining the standard input protocol volumes of DNA input and bead-linked transposomes PCR-free (BLT-PF) with low input single-sided bead purification (1.8x ratio) was determined to be optimal for obtaining libraries of an ideal size and with sufficient quantity for sequencing (Table 2). Libraries prepared with as low as 50 ng of input gDNA were sequenced on a NovaSeq S4 PE150. The 1.8x ratio resulted in the kit’s expected insert size of ~450 bp for >300 ng input. BLT-PF and DNA input volumes will need to be further adjusted for 50 ng input to achieve the expected insert size in both manual preparation and the automated workflow on MIRO CANVAS.

*NA12878 gDNA samples were obtained from the NIGMS Human Genetic Cell Repository at the Coriell Institute for Medical Research.

Table 1: Conditions for sample purification bead addition and insert size selection across different inputs of DNA tested.

Table 2: Library insert sizes and yields generated from different inputs of unsheared NA12878 DNA.

Illumina DNA PCR-free libraries prepared from a range of DNA inputs using either manual or MIRO CANVAS preparation methods demonstrate comparable % Q30 score, autosome callability, % mapped reads, % of bases covered at 20X, coverage uniformity and % unique reads.

The resulting sequencing metrics values are comparable between manually prepared libraries and those generated using the automated workflow on MIRO CANVAS (Figure 2). For DNA input amounts >300 ng, MIRO CANVAS libraries match or exceed the sequencing metrics for manual libraries including base call accuracy, passing genotype calls in autosomal chromosomes, reads that confidently map to the reference genome, the % of bases covered at 20X, uniformity of coverage and duplication rates. QC metrics used in applications aimed at variant detection were additionally examined after subsampling to 40X sequencing coverage (Table 3). MIRO CANVAS libraries presented equal or better F1 scores for both SNVs and INDELs, as well as % bases covered at 20X across all input ranges of tested DNA input.

Table 3: The performance of QC metrics relevant for variant calling across a range of input DNA. All samples were subsampled to 40X sequencing coverage.

MIRO CANVAS walk away automation reduces hands-on time

The total time required for library preparation with the Illumina DNA PCR-Free Prep kit is 25 minutes greater when automating on MIRO CANVAS, but the hands-on time is considerably less than for manual preparation workflows (Table 1). Automation with MIRO CANVAS reduces hands-on time to zero for the tagmentation, post-tagmentation cleanup, ligation, and library cleanup steps.

References

1. Kebschull JM et al. Nucleic Acids Res 2015; 43 (21): e143.
2. Yoo J et al. Poster 32 presented at the Association of Biomolecular Resources Facilities (ABRF) 2021 Virtual Annual Meeting; 7–11 March 2021.
3. Illumina DNA PCR-Free Prep. Available at: https://www.illumina.com/products/by-type/sequencing-kits/library-prep-kits/dna-pcr-free-prep.html accessed April 2021.