Whether your focus is crop or livestock breeding, genetic engineering, or pest and disease mitigation, HiFi sequencing delivers genomic data of unparalleled quality and detail to meet the demands of your most ambitious research programs.
Use HiFi sequencing to breed better by quickly assembling phased reference-quality genomes for the imputation of the most desirable complex traits.
Genetic engineering of plants and animals
Create high-quality reference genomes, validate constructs, confirm edits, and evaluate off-target effects quickly and reliably with HiFi reads.
Pest and disease research
Dig into genomes and transcriptomes of the highest quality and specificity. Uncover hard-to-find novel genes responsible for traits like immunity, metabolic detoxification, and pesticide resistance.
Tackle global challenges to feed a growing population
As the challenges of a growing global population and a changing climate mount, cutting-edge agricultural biotechnology is needed to drive scientific advances to sustainably feed our world.
At PacBio, we provide state-of-the-art genome sequencing solutions that enable you to uncover and harness agrigenomic insights from data of unparalleled quality and detail.
Use these biological insights to enhance marker development, facilitate the production of more nutritious foods, safe-guard crop and livestock health, and increase agricultural yields for the world of tomorrow, today.
Common questions about genomics in agriculture
Agrigenomics in action
Soybean pangenome captures genetic diversity
Learn how HiFi reads were used to identify key structural variants for functional studies and breeding of one of the world’s most important sources of protein.
Whole genome sequencing best practices
See recommended workflows for procuring reference-quality genomes, de novo.
HiFi sequencing for a better view into the bovine genome
Evaluate how HiFi sequencing was used to assemble a bovine pangenome with hundreds of structural variants important to phenotype — all while achieving coverage, quality, accuracy, and completeness metrics that cannot be matched.
“…high-quality [HiFi] genomes enabled the identification of numerous complex variations that cannot be detected by simply mapping short reads to a single genome…”—Yucheng Liu et al., Cell 2020
Agrigenomics for crop and livestock breeding
Unlock whole-new capabilities for your plant or animal breeding programs with long, high-quality, genomic reads made possible only with HiFi sequencing.
• Build reference-quality, haplotype-resolved pangenomes for breeding.
• Impute desirable traits to SNPs, structural variants, and complex genotypes.
• Capture genomic variants on a genome-wide scale for outbreds, inbreds, and populations.
Agrigenomics for genome engineering
Obtain the detailed sequence information you need for your most sophisticated gene editing programs using highly accurate HiFi sequencing data.
• Speed up design workflows with accurate reference genomes.
• Find splice variants within the transcriptome.
• Validate edited sites.
• Capture on and off-target effects.
• Determine structural rearrangements across chromosomes.
Agrigenomics for pest and disease research
Find genomic clues hidden in the highly variable genetics of organisms such as insects, weeds, and fungi harming agricultural yield to tackle pests on the molecular level.
• Capture pest genomic diversity in incredible detail.
• Generate complete genome assemblies from just 5 ng of DNA input.
• Build annotations to better understand gene functions for targeting.
PacBio vs Oxford Nanopore*
Long-read sequencing performance
|PacBio HiFi sequencing||Oxford Nanopore|
Coverage required to meet quality targets
|19x diploid||56x diploid|
|CPU hours required||600||2,200|
|Peak memory usage required||200 GB||750 GB|
*Alexander S. Leonard, Danang Crysnanto, Zih-Hua Fang, Michael P Heaton, Brian L. Vander Ley, Carolina Herrera, Heinrich Bollwein, Derek M. Bickhart, Kristen L. Kuhn, Timothy PL. Smith, Benjamin D. Rosen, Hubert Pausch. Structural Variant-based Pangenome Construction has Low Sensitivity to Variability of Haplotype-resolved Bovine Assemblies. [Preprint] bioRxiv 2021.11.02.466900; doi: https://doi.org/10.1101/2021.11.02.466900
Whole genome sequencing
Quickly and affordably create contiguous, complete, and correct de novo assemblies of even the most complex genomes.
Structural variant calling
Acquire high-sensitivity variant calls with low false discovery rates to gain actionable insights across populations.
Combine long-read sequencing with targeted sequence capture for a comprehensive view of specific genomic regions of interest, regardless of size.