Product Description
Nucleic Acid Sequencing makes up a strand of DNA, adenine, guanine, cytosine, and thymine, which are precisely ordered via a process called DNA sequencing. These bases offer the underlying genetic basis for directing a cell's actions, location, and type. This is tested under various parameters to ensure its high quality and effectiveness. Nucleic Acid Sequencing is very safe to use. Every person and the living thing has a unique nucleotide base sequence. For many basic and practical research applications nowadays, it is a crucial tool.
High-Throughput Multiplex SequencingThe Sequencer X1000 is capable of processing up to 96 barcoded samples simultaneously, enabling massive data generation with high accuracy in a single run. With a maximum throughput of 3 billion reads per run, it is well-suited to laboratories requiring efficient and scalable sequencing solutions for various research and diagnostic applications.
Comprehensive Data Connectivity and OutputSupporting Ethernet, USB, and WiFi, the Sequencer X1000 ensures seamless data transfer and integration into modern laboratory workflows. Generated sequencing data is available in FASTQ, BAM, and VCF file formats, providing compatibility with diverse analytical and bioinformatics platforms. This flexibility supports comprehensive downstream analysis and data management.
Fully Automated and Precise OperationEngineered with automation in mind, the Sequencer X1000 delivers streamlined workflows. With a processing speed of up to 600 Mb/hour and read accuracy exceeding 99.99%, it maintains rigorous standards essential for research and clinical labs. Easy compatibility with standard sequencing reagents and cartridges further simplifies operation and reduces hands-on time.
FAQs of NUCLEIC ACID SEQUENCING:
Q: How does the barcode capability benefit sequencing workflows?
A: The barcode capability allows processing up to 96 samples in one run by uniquely tagging each sample. This multiplexing increases throughput, reduces costs, and simplifies sample tracking and downstream analysis.
Q: What types of data output formats are supported by the Sequencer X1000?
A: The instrument generates data in FASTQ, BAM, and VCF formats, ensuring compatibility with a wide array of bioinformatics tools for quality assessment, alignment, and variant analysis.
Q: When is it recommended to use the Sequencer X1000s multiplexing feature?
A: Multiplexing is best used when handling high sample volumes, such as in large-scale research projects or clinical studies, enabling all samples to be processed together efficiently and cost-effectively.
Q: Where can the Sequencer X1000 be installed, given its noise and size specifications?
A: With a compact footprint (780 mm x 600 mm x 900 mm) and noise level under 60 dB, the instrument can be conveniently installed in standard molecular biology laboratories without the need for additional soundproofing.
Q: What is the typical process for using the Sequencer X1000?
A: Users prepare sample libraries with barcodes, load them into compatible cartridges with standard reagents, initiate the fully automated run, and collect data via Ethernet, USB, or WiFi upon completion. Automated workflows enhance reproducibility and reduce manual effort.
Q: How does the integrated automation grade improve sequencing efficiency?
A: Full automation minimizes manual intervention, reduces human error, and streamlines sequencing, helping laboratories achieve faster turnaround times with consistently reliable results.
Q: What are the primary benefits of using the Sequencer X1000 for exporters, importers, and suppliers in India?
A: The Sequencer X1000 is CE and ISO 13485 compliant, energy-efficient, and user-friendly, making it a reliable solution for diverse commercial applications that require accurate, high-throughput sequencing while meeting international safety and performance standards.