By integrating Genotyping-by-Sequencing (GBS) for comprehensive genetic discovery with targeted amplicon sequencing panels, our solution efficiently identifies optimal genetic combinations. This integrated approach enables the rapid development of improved crop varieties with enhanced traits such as disease resistance and yield potential, accelerating progress toward sustainable agricultural systems.
Our GBS & Marker-Assisted Selection provides a comprehensive and cutting - edge approach to modern agricultural breeding. GBS is a high - throughput, cost - effective genotyping method that allows for the simultaneous discovery and genotyping of thousands of genetic markers across the genome. The AgriSeq Panel provides a targeted approach, focusing on a curated set of key genetic markers. When combined with broader genomic analyses, these technologies work together to give us a complete and precise picture of genetic makeup. This integrated strategy enables faster, more efficient breeding by guiding selection with accuracy.
Our GBS & Targeted Panel Solution for Marker-Assisted Salection Empowers Your Agricultural Breeding with:
Genotyping-by-Sequencing (GBS) & Marker-Assisted Selection are vital in modern agri-research. GBS is a high-throughput genotyping method, discovering numerous genetic markers across the genome. Marker-assisted selection uses these markers to predict trait expression. By analyzing gene loci related to yield, quality, etc., it reveals gene-trait links. This combination accelerates breeding of high-yield varieties, boosting agricultural productivity and sustainability.
1. Diverse Germplasm Collection & Phenotyping
We start by building a diverse germplasm panel that includes wild relatives, landraces, and elite varieties. Each sample is paired with high-quality phenotypic data for traits like yield and stress tolerance. Collected from various environments, these samples enable the discovery of locally adapted alleles. We also integrate multiple molecular layers (e.g., transcriptomics, metabolomics) from relevant tissues for a holistic, multi-omics view.
2.Multi-Tissue and Multi-Omics Integration
To build a holistic view of the genotype-to-phenotype map, we often employ a multi-omics strategy. During collection, we sample relevant tissues (e.g., roots under drought stress, seeds for quality analysis, animal blood or muscle). We integrate genomic data with other molecular layers, such as transcriptomics (gene expression) and metabolomics (biochemical profiles), alongside detailed environmental records.
1. Genotyping-by-Sequencing (GBS) for Discovery and Diversity
How We Deliver: GBS uses restriction enzymes to reduce genome complexity, followed by high-throughput sequencing to genotype thousands of markers across the genome. This is our go-to method for initial genetic diversity assessment, constructing genetic maps, and conducting genome-wide association studies (GWAS) in populations without a pre-existing reference panel.
Application: It is exceptionally cost-effective for screening large populations at the early stages of a breeding program. We use GBS to uncover novel genetic variants, analyze population structure, and identify genomic regions associated with traits in unstructured or highly diverse germplasm collections.
2. Custom Targeted Panels for High-Throughput, Application-Focused Genotyping
How We Deliver: Leveraging discoveries from our GBS data and public repositories, we design custom targeted genotyping panels. These panels utilize a highly multiplexed, amplicon-based sequencing approach to focus on a curated set of known, trait-relevant markers, ensuring exceptional genotyping accuracy, reproducibility, and cost-efficiency for large-scale screening.
Application: This method forms the core of our applied marker-assisted selection (MAS) pipeline. Once key marker-trait associations are validated, we deploy these custom panels for routine, high-throughput genotyping in advanced breeding generations. This facilitates the rapid and precise selection of superior individuals carrying desirable alleles for traits such as disease resistance, quality, and stress tolerance, thereby dramatically accelerating the breeding cycle.
1. Population Genomics & Genetic Architecture
We start with stringent quality control (using tools like PLINK) to clean the data. We then analyze population structure to clarify genetic relationships and ancestry. This allows you to make informed crossing decisions, manage genetic diversity, and avoid spurious associations in later analyses.
2. Selection Signature & Genomic Selection
We scan the genome for signatures of selection using statistical methods like XP-CLR (Cross-Population Composite Likelihood Ratio) and iHS (Integrated Haplotype Score). This reveals genomic regions that have been under historical selection pressure, highlighting genes that contributed to the improvement of traits like grain size or animal growth rate. Furthermore, we use the genome-wide marker profiles to build Genomic Selection (GS) models. These models calculate Genomic Estimated Breeding Values (GEBVs), allowing breeders to select individuals based on their total genetic potential at the seedling stage, long before phenotypic evaluation.
3. Gene-Trait Association & Functional Annotation
Which specific gene variants control my trait of interest? We perform GWAS to find statistically robust associations. We then annotate these variants to understand their potential biological effect (e.g., if they disrupt a protein), giving you a shortlist of high-confidence candidate genes to target in your program.
Figure 1: How We Deliver This Solution: GBS & Marker-Assisted Selection Workflow
GBS uses restriction enzymes to reduce genome complexity, allowing for the sequencing and genotyping of thousands of markers across the genome at a fraction of the cost of whole-genome sequencing. This makes high-density genotyping accessible for large breeding populations, which is essential for powerful statistical analysis.
Unlike array-based technologies that rely on pre-defined markers, GBS is a discovery platform. It can identify novel SNPs and insertions/deletions (InDels) directly within any germplasm, including wild relatives and local landraces. This is crucial for uncovering unique alleles associated with valuable traits in underutilized or locally adapted genetic resources.
GBS is exceptionally valuable for non-model organisms or crops with limited genomic resources. It does not require a pre-existing reference genome to generate a large number of markers, enabling the implementation of modern MAS in species that were previously lacking genetic tools.
The GBS protocol seamlessly integrates the discovery of new genetic variants with the genotyping of individuals in a single, streamlined workflow. This eliminates the need for separate, costly discovery phases and accelerates the transition from initial genetic studies to applied breeding.
The high density of markers generated by GBS allows for the construction of very precise genetic linkage maps. These improved maps enhance the accuracy of Quantitative Trait Loci (QTL) mapping, leading to the identification of candidate genes with higher confidence and a better understanding of complex trait architecture.
GBS provides a genome-wide snapshot of genetic variation that is ideal for robust population genetics analyses. It allows breeders to accurately quantify genetic diversity, understand population structure, and identify genetic relationships, which informs decisions on parental selection and germplasm conservation.
The dense, genome-wide marker data from GBS is the perfect input for building Genomic Selection models. These models use all markers to calculate Genomic Estimated Breeding Values (GEBVs), allowing for the selection of superior individuals based on their genetic potential alone, dramatically accelerating the breeding cycle for complex, polygenic traits.
Reproductive efficiency is a key factor in livestock production. GBS can help identify genetic variants related to reproductive traits in pigs, such as litter size and age at puberty. The AgriSeq Panel can be used to screen pig populations for these markers. Farmers can increase the number of piglets per sow and reduce the time to first breeding, thereby improving the overall productivity of the pig herd.
GBS is a powerful tool for GWAS in diverse natural populations or association panels. It detects genome-wide markers that are significantly associated with specific phenotypes. This approach leverages historical recombination events to identify marker-trait associations with much higher resolution than traditional QTL mapping, facilitating the discovery of alleles for disease resistance or quality traits from diverse genetic backgrounds.
For traits controlled by many genes with small effects (polygenic traits), GBS provides the genome-wide marker density required for Genomic Selection. Researchers use GBS data to build prediction models that calculate Genomic Estimated Breeding Values (GEBVs) for individuals. This allows for selection based on genetic potential early in the lifecycle (e.g., at the seedling stage), significantly accelerating the breeding cycle.
GBS facilitates the introgression of one or a few major genes (e.g., for disease resistance) from a donor into an elite recipient line. The dense markers allow for both foreground selection (to ensure the target gene is present) and background selection (to rapidly recover the recipient genome). Similarly, GBS data is used to pyramid multiple beneficial genes from different sources into a single elite genotype.
Figure 2: Comparison of mean annual aggregated genetic gain (a), total breeding value (TBV) and variance (b) across different parental selection strategies, including Stage 2 (STG2) with phenotypic selection (PS), and STG2, F6, F2, or F1 generations with genomic selection (GS) using single-seed-descent (SSD) or accelerated SSD (aSSD) methods. (Li, 2022)
Marker-Assisted Introgression of the Salinity Tolerance Locus Saltol in Temperate Japonica Rice.
Journal: Rice (N Y)
Published:2023
Abiotic stresses, particularly salinity, pose a significant threat to global crop production, with over 50% of crop yields negatively impacted and at least 33% of arable lands affected by salinization. The situation is expected to worsen due to global climate changes, which increase sea water intrusion, evaporation, and exacerbate salinity-related problems through factors like incorrect soil drainage, use of poor-quality water, and increased capillarity rise of saline groundwater. Rice, a staple crop, is highly sensitive to salt at various growth stages, with salt causing osmotic and ion stresses that disrupt metabolic processes, affect plant growth, development, and yield. The detrimental effect of salinity on young rice seedlings is especially concerning as it directly influences plant establishment and, consequently, crop yield.
To enhance salinity tolerance in rice, we focus on the Saltol QTL—a major genetic locus on chromosome 1 that is pivotal for seedling-stage salt tolerance. It functions primarily by regulating sodium-potassium homeostasis, a trait largely attributed to the OsHKT1;5 gene. The efficacy of this locus has been consistently proven through both marker-assisted breeding and transgenic validation.
Significant progress has been made in the identification and validation of salt-tolerant genes and quantitative trait loci (QTLS) in rice. Saltol QTL can enhance the salt tolerance at the seedling stage of a series of high-yield indica rice varieties. Additionally, functional validation studies using transgenic technology have confirmed the role of specific genes within the Saltol QTL in conferring salt tolerance. Notably, a recent study evaluated the effects of introgressing the Saltol QTL into japonica rice varieties using a Marker Assisted Back-Cross (MABC) approach, further expanding our understanding of its potential in different genetic backgrounds. These scientific achievements provide a solid foundation for developing salt-tolerant rice varieties that can contribute to global food security in the face of increasing salinity and climate change.
Figure 3: Comparison of the performances of 96 KASP marker panel and GBS in evaluating the RP genome recovery in the selected BC3F4 introgression lines.
The AgriSeq Panel is designed to precisely detect genetic variations associated with specific traits. Our process is as follows: First, identify the target gene, and then design and optimize the detection probe. The entire panel must undergo strict computer simulation and wet test verification to ensure its specificity, sensitivity and stability, and ultimately deliver a highly reliable analytical tool. This optimization process may involve adjusting primer concentrations, annealing temperatures, and other reaction conditions.
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