Inexpensive Multiplexed Library Preparation for Megabase-Sized Genomes

BioRxiv : the Preprint Server for Biology
Michael BaymRoy Kishony

Abstract

Whole-genome sequencing has become an indispensible tool of modern biology. However, the cost of sample preparation relative to the cost of sequencing remains high, especially for small genomes where the former is dominant. Here we present a protocol for the rapid and inexpensive preparation of hundreds of multiplexed genomic libraries for Illumina sequencing. By carrying out the Nextera tagmentation reaction in small volumes, replacing costly reagents with cheaper equivalents, and omitting unnecessary steps, we achieve a cost of library preparation of $8 per sample, approximately 6 times cheaper than the widely-used Nextera XT protocol. Furthermore, our procedure takes less than 5 hours for 96 samples and uses nanograms of genomic DNA. Many hundreds of samples can then be pooled on the same HiSeq lane via custom barcodes. Our method is especially useful for re-sequencing of large numbers of full microbial or viral genomes, including those from evolution experiments, genetic screens, and environmental samples.

Related Concepts

Environment
Genome
Adverse Reaction to Drug
Viral Genome
Small Molecule Libraries
Research Study
Re-evaluation
Genetic Screening (Procedure)
Nucleic Acid Sequencing
Molecular Genetic Technique

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