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  • Low-pass WGS and Imputation Analysis
    • Low-pass WGS and Imputation Analysis
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Low-pass WGS and Imputation Analysis

Low-pass WGS and imputation analysis provide a scalable approach to genome-wide genotyping for plant and animal breeding research. By sequencing across the genome at low coverage — typically 0.5x to 5x — and using imputation to infer missing genotypes, researchers can access broad genomic information while helping reduce sequencing costs compared with high-depth whole genome sequencing.

Explore solutions that support key steps in low-pass WGS workflows, from sample homogenization and nucleic acid extraction to library preparation, automation, and imputation analysis.

Planning a low-pass WGS genotyping project?

Low-pass WGS workflows can vary based on sample type, throughput, sequencing strategy, automation needs, and imputation requirements. Connect with us to discuss solutions that fit your workflow.
 

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  Low-pass WGS High-depth WGS SNP arrays
Sequencing coverage Low High N/A
Relative cost per sample Low High Low
Prior variant knowledge required No No Yes
Novel variant detection Yes Yes  Limited
Genome-wide information Broad Comprehensive Limited to array content
CNV detection potential  Yes Yes Limited
Imputation analysis Commonly used Optional  Not typically required

 

Low-pass WGS workflows require coordination across sample preparation, DNA extraction, quality control, library preparation, automation, and downstream analysis. Each step can influence throughput, data quality, and the ability to generate reliable results for imputation.

For research use only. Not for use in diagnostic procedures.

low-pass-whole-genome872x872

Workflow solutions for low-pass WGS and imputation analysis

From challenging plant and animal sample types to high-throughput library preparation and downstream genotype imputation, each step can affect the quality and usability of low-pass WGS data. Integrated workflow solutions can help support consistent sample processing, efficient library preparation, scalable automation, and analysis-ready results.

Sample homogenization

Plant tissues, seeds, animal tissues, and other agricultural inputs can be difficult to process consistently. Variability at this first step can carry through extraction, library preparation, sequencing, and downstream analysis. Homogenization solutions for plant and animal samples can help create more uniform starting material, supporting reliable DNA recovery across large genotyping studies.

Homogenization solutions for plant and animal samples can help create more uniform starting material, supporting reliable DNA recovery across large genotyping studies.

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Nucleic acid extraction

Successful genotyping studies depend on DNA that is suitable for efficient library preparation and sequencing. Agricultural samples can introduce challenges such as variable tissue composition, inhibitors, degraded inputs, or inconsistent yields.

Scalable extraction workflows help labs process diverse sample types while maintaining the consistency needed for high-throughput projects.

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Sample and library quality control

Poor sample or library quality can reduce the usefulness of sequencing data before analysis begins. QC checkpoints help confirm that DNA inputs and prepared libraries are suitable before committing samples to sequencing.

Assessing concentration, quality, and library size distribution can help identify failed or variable samples earlier, reduce wasted sequencing capacity, and support more consistent data generation.

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DNA library preparation

Library preparation is a key step in generating sequencing-ready DNA for low-pass WGS genotyping. Efficient library conversion, compatibility with commonly used sequencing platforms, and support for variable sample quality are important considerations for agricultural research workflows.

NEXTFLEX® HT Agrigenomics Low-Pass WGS kits are designed to support high-throughput library preparation from breeder-relevant DNA samples and generate libraries compatible with Illumina® and Element® sequencing platforms.

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Modular and scalable automation

As low-pass WGS projects scale, manual steps can limit throughput and introduce variability. Automation can help standardize key workflow steps, improve efficiency, and support consistent processing across larger sample sets.

Modular automation solutions can be configured to support different throughput needs across sample preparation, nucleic acid extraction, QC, and library preparation workflows.

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Imputation analysis

Low-pass WGS generates genome-wide sequencing data at reduced coverage, making imputation an important step for inferring missing genotypes and producing more complete variant information.

CURIO analysis solutions can help support low-pass WGS data interpretation, converting sequencing data into genotype information for downstream breeding research applications.

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Featured resources

Webinar

A streamlined approach to genotyping with low pass WGS on-demand webinar

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Application note

Modernizing molecular breeding with low-pass WGS

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Flyer

A streamlined approach to genotyping with low-pass WGS

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Application note

Efficient low‑pass whole genome sequencing on the Ultima Genomics UG 100 sequencing platform

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Explore our solutions

library-prep-kits-512x288

ライブラリー調製キット

次世代シーケンス(NGS)において信頼性の高い結果を得るためには、堅牢なライブラリー調製が重要なステップとなります。
Learn more
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FAQs

  • When is low-pass WGS a good fit for genotyping studies?

    Low-pass WGS can be a good fit when researchers need genome-wide genotyping across large sample sets but do not require high-depth sequencing for every sample. It is commonly used in plant and animal breeding research where cost, throughput, and broad genomic coverage are important considerations.

  • How does low-pass WGS differ from SNP arrays?

    SNP arrays analyze a predefined set of markers, so they depend on prior knowledge of the variants included on the array. Low-pass WGS sequences across the genome at reduced coverage, which can provide broader genomic information and more flexibility across populations, species, or breeding programs.

  • Why is imputation used with low-pass WGS?

    Because low-pass WGS sequences the genome at reduced coverage, not every genotype is directly observed. Imputation uses the available sequencing data and a reference panel or population-level information to infer missing genotypes and generate more complete variant information for downstream analysis.

  • What factors can affect imputation results?

    Imputation performance can be influenced by sample quality, sequencing data quality, coverage level, variant density, population structure, and the quality and relevance of the reference panel. A well-designed workflow helps generate data that is more suitable for reliable downstream interpretation.

  • Can low-pass WGS be used for both plant and animal breeding research?

    Yes. Low-pass WGS can be applied to plant and animal breeding research, but workflow requirements may vary depending on sample type, genome complexity, available reference resources, and project goals. Upstream sample preparation and downstream imputation strategy should be matched to the specific study design.

Featured products

Adapters for NGS sequencing and multiplexing compatible with Illumina and Element systems.
NEXTFLEX HT Agrigenomics Low-pass WGS Kit
Part number: NOVA-5141-70, NOVA-5141-71, NOVA-5141-72, NOVA-5141-73, NOVA-5141-74
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