Contract analysis of a novel genotyping technology GRAS-Di(R) using random PCR.
Our company conducts library preparation, sequencing, and data analysis for GRAS-Di(R) by sending us DNA samples. The new marker technology GRAS-Di(R) (Genotyping by Random Amplicon Sequencing-Direct) utilizes next-generation sequencing and is a novel method for genotyping that determines the sequences of multiple locations in the genome through PCR amplification using random primers. It can be used for marker discovery, marker selection, QTL analysis, linkage mapping, and more. 【Features of GRAS-Di(R)】 ■ Reduces missing values due to good reproducibility of amplicon amplification efficiency ■ Achieves genome-wide fragment amplification through random PCR *For more details, please download the PDF or feel free to contact us.
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Flow of genotyping analysis using GRAS-Di(R) 1. Library preparation by random PCR 2. Sequencing 3. Data analysis - Analysis using GRAS-Di(R) software - Mapping analysis (optional) *For more details, please download the PDF or feel free to contact us.*
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【Utilization of GRAS-Di(R) Analysis Data】 ■Linkage Map ■Marker Search ■QTL Analysis ■GWAS Analysis, etc. *For more details, please download the PDF or feel free to contact us.
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Our company provides advanced omics analysis, including next-generation sequencing (NGS), to support your research and business. Additionally, we design and develop omics analysis-related software systems tailored to your needs. Please feel free to contact us if you have any requests.