Haplotype-Phased Synthetic Long Reads from Short-Read Sequencing.
Where this comes from
- Record sourced from PubMed, PMID 26789840.
- Also identified by DOI 10.1371/journal.pone.0147229 and PMC identifier 4720449.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Next-generation DNA sequencing has revolutionized the study of biology. However, the short read lengths of the dominant instruments complicate assembly of complex genomes and haplotype phasing of mixtures of similar sequences. Here we demonstrate a method to reconstruct the sequences of individual nucleic acid molecules up to 11.6 kilobases in length from short (150-bp) reads. We show that our method can construct 99.97%-accurate synthetic reads from bacterial, plant, and animal genomic samples, full-length mRNA sequences from human cancer cell lines, and individual HIV env gene variants from a mixture. The preparation of multiple samples can be multiplexed into a single tube, further reducing effort and cost relative to competing approaches. Our approach generates sequencing libraries in three days from less than one microgram of DNA in a single-tube format without custom equipment or specialized expertise.
Medical subject headings
- Algorithms
- Genome
- Haplotypes
- High-Throughput Nucleotide Sequencing
- Sequence Analysis, DNA