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The "SNV screening system V.2025" is a web analysis system that detects candidate genes from SNV information of multiple samples. It stores the called SNV information of multiple samples in a relational database, allowing users to set various filtering conditions via the web and perform searches, enabling the listing of candidate genes related to phenotypes. The data of the called SNVs is imported into the RDB, followed by preprocessing for annotation assignment and filtering searches. 【Features】 ■ Import SNV data (in VCF format) into RDB ■ Create unique variant data ■ Curated annotation information ■ Grouping of search target samples and saving of search conditions, as well as the ability to perform set operations on SNVs *For more details, please refer to the PDF document or feel free to contact us.

• Other information systems

The "Bio Big-AnalysysPac RMS" is a storage server designed to store large amounts of biological information. It is provided as a rack-mounted large-scale storage server for storing massive data. Please feel free to consult us when you need assistance. 【Specifications Example】 ■Storage (Main Unit): 20TB 6Gb/s SATA HDD (high durability) × 16 units RAID6 Total usable capacity approximately 252TB (20TB × (16-2) × 0.9) ■HDD Bay: (3.5"): [Hot Swap Bay for SAS/SATA HDD] 20TB SATA HDD × 16 bays ■IPMI: IPMI (Intelligent Platform Management Interface) for Remote System Power on/off and system monitoring *For more details, please refer to the PDF document or feel free to contact us.

• Other information systems

"Ansrch" is a gene catalog database that provides vast amounts of annotation information as a web system. It organizes rich annotations, making them easy to search and reference. Since it is a system that can be accessed using a web browser, information can be shared not only within an organization but also among multiple researchers. [Benefits] ■ Gene prediction - Predictions regardless of expression levels ■ RNA-seq - The obtained nucleic acid sequences are real transcription sequences (with evidence of expression) - Contains UTR - High likelihood of obtaining transcription start points *For more details, please refer to the PDF materials or feel free to contact us.

• Other information systems

(1) Annotation using BLAST against NCBI-nr (2) Annotation using EggNOG, which is an OrthologDB (3) Annotation using InterPro (5) Utilization of RNA-seq reads

• others

Our company offers a "Next-Generation Sequencer Contract Analysis Service" that covers the processes of sequencing, narrowing down candidate genes, and data evaluation. Based on extensive knowledge, our expert staff supports the selection of analysis methods tailored to research themes, including data evaluation after analysis. Through our consistent service, we can provide solutions that lead to your research outcomes. 【Features】 ■ Consideration and implementation of contract analysis methods using next-generation sequencers ■ High-quality sequencing and advanced data analysis, with a variety of analysis options available ■ Presentation of gene lists according to research objectives to facilitate smooth research progress ■ Programs that allow for BLAST searches and ID searches can also be proposed *For more details, please refer to the materials. Feel free to contact us with any inquiries.

• Contract Analysis

The KM Data Corporation's "Key Molnet Lite" is a tool for interpreting candidate genes and narrowing down options based on their significance. By inputting candidates obtained from measurement results, it allows for the refinement and interpretation of candidates, as well as the discovery of important candidates that may not be evident from the measurement results. 【Features】 ■ Stores only information that has been carefully reviewed by humans from research papers ■ Thorough examination of molecular names ■ Visualization of numerical data ■ Abundant annotations gathered from research papers ■ Diverse search menus ■ User-friendly interface For more details, please refer to the catalog or feel free to contact us.

• others

The "Subio Platform" is a high-performance and user-friendly browser specifically designed for omics data by Subio Corporation. Anyone can download it for free and use it intuitively with simple operations. Additionally, since the analysis results are saved in the "Subio Platform," you will not lose access to your data even if the license for the extended features (paid) expires. Furthermore, our company offers high-performance analysis tools that excel in workflow processes, such as the "Subdive" system, which visualizes vast amounts of genomic variation and polymorphism data, and is oriented towards discussion. 【Product Lineup】 ■ Extended Feature: Basic Plug-in A package of basic statistical analysis tools for expression data analysis. ■ Extended Feature: Advanced Plug-in A package of analysis functions useful for biologically interpreting the results of statistical analysis. ■ Subrium Allows centralized management and sharing of large and diverse omics data, among others. For more details, please refer to the catalog or feel free to contact us.

• others