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We offer various sequencing contract services using Oxford Nanopore Technologies' nanopore sequencer. The sequencer provided by the company measures changes in current that occur when DNA or RNA molecules pass through nanopores formed by proteins embedded in a polymer membrane. By not using fluorescent dyes or DNA polymerases that were used in existing sequencers, it has succeeded in miniaturizing the device and is characterized by the ability to obtain very long sequences. 【Services Offered】 ■ Whole Genome Sequencing ■ Whole Transcriptome Sequencing ・ cDNA-seq ・ direct RNA-seq *For more details, please download the PDF or feel free to contact us.
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Free membership registrationOur 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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Free membership registrationWe offer contract analysis services in Japan using the MGISEQ-2000 (DNBSEQ-G400) from MGI Tech. DNBSEQ sequences libraries that are adjusted through rolling circle amplification (RCA) using circular single-stranded DNA as a template. It not only reduces the accumulation of PCR errors and GC bias that occur during library amplification on other existing sequencing platforms but also mitigates issues such as PCR duplicates and index hopping. 【Service Details】 ■ Whole Genome Sequencing (WGS) ■ RNA Sequencing (stranded mRNA-seq) ■ stLFR (single tube Long Fragment Read) sequencing ■ Lane sequencing by library submission *For more details, please download the PDF or feel free to contact us.
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Free membership registration"GGM (GenaGenomeManager)" is a data storage system that provides comprehensive support for managing, viewing, and analyzing the ever-increasing NGS data. Based on registered BAM data, it allows for the creation of projects with flexible combinations, detection of variants, and analysis of expression information, with results that can be searched and viewed graphically. Additionally, by registering metadata such as trait information, it facilitates the exploration of variants and genes with expression fluctuations that correlate with traits. 【Product Overview】 - A server-integrated system capable of registering data on the scale of 1000 samples - A lightweight and user-friendly interface that allows for easy comparison of multiple datasets - Unused data can be stored offline on external hard drives - No limit on the number of users; can be used by multiple people on their respective computers - Access restrictions at the workspace level to ensure data confidentiality, among other features *For more details, please download the PDF or feel free to contact us.
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Free membership registrationThis catalog is a comprehensive catalog featuring the analysis systems and next-generation sequencing services provided by GeneBay Inc. We introduce various systems and services, including the hardware-integrated system "GenaGenomeManager(TM)" that enables efficient accumulation, management, and analysis of NGS data, the genome database cloud "GiNeS," and other sequencing data analysis cloud services. [Contents] ■ Analysis Systems ■ Next-Generation Sequencing Services *For more details, please download the PDF or feel free to contact us.
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