next-generation-dna-sequencing Downloads
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You're in control with Sequencher's powerful, user-friendly tools and features. Sequencher is intuitive, so each step from importing your reads to assembly to searching for SNPs and heterozygotes is straightforward. Sequencher is flexible. You can adjust parameters and preferences and save them to easily standardize your ...
miRNA sequencing, based on next-generation sequencing (NGS), can comprehensively profile miRNA sequences, either known or novel miRNAs. Our miRNA sequencing detects novel miRNAs as well as isomiR, enabling you to see precisely which miRNA sequences are expressed in your samples and uncover the importance of these small regulatory elements linked to a wide range of biological functions. ...
The HUMAN TCR RNA MULTIPLEX kit is designed for the amplification of TCR alpha and beta cDNA libraries using the combination of highly sensitive multiplex PCR and Unique Molecular Identifiers (UMIs). UMIs are introduced along with 1st strand cDNA synthesis and allow for advanced PCR and sequencing error correction, elimination of PCR biases, exact quantification of template cDNA molecules, and ...
The Monkey TCR RNA Kit is designed for unbiased amplification of TCR alpha and beta cDNA libraries using 5’RACE (Rapid Amplification of cDNA Ends) with unique molecular identifiers (UMI) incorporated within template switch oligo. 5’RACE UMI technique allows for advanced PCR and sequencing error correction, exact quantification of template cDNA molecules, and accurate normalization of ...
The Mouse α/β TCR RNA Kit is designed for unbiased amplification of TCR alpha and beta cDNA libraries using 5’RACE (Rapid Amplification of cDNA Ends) with unique molecular identifiers (UMI) incorporated within template switch oligo. 5’RACE UMI technique allows for advanced PCR and sequencing error correction, exact quantification of template cDNA molecules, and accurate ...
Speed and throughput flexibility across a broad range of NGS ...
To bring next-generation sequencing (NGS) in-house, you need a solution that is truly easy to implement and easy to use—one that can help you surmount the current barriers and redefi ne in-house ...
To bring next-generation sequencing (NGS) in-house, you need a solution that is truly easy to implement and easy to use—one that can help you surmount the current barriers and redefi ne in-house ...
Lexogen is a biotech company that provides innovative solutions for one of the fastest developing technologies in the last decade – Next Generation Sequencing (NGS). The company’s main focus is the development of RNA sequencing technologies to resolve the complexity of the transcriptome. Lexogen was founded in 2007. The headquarters of the company are located in Vienna, Austria, and ...
FUSION GENOMICS ONETest platform offers a complete 12 hours “Benchtop to Desktop” solution for next generation sequencing based diagnostic testing of infectious diseases. The ONETest platform comprises our patent pending and proprietary UNIPrep, QUANTUMProbes and the FUSIONCloud with 1000X the sensitivity over PCR and up to 9000X target enrichment over metagenome sequencing. The ...
CD Genomics, an advanced sequencing service provider equipped with extensive technologies and knowledge in phageome, is now ready to provide comprehensive Phage Genome Sequencing and Metagenomics Services. https://www.cd-genomics.com/Microbial-Whole-Genome-Sequencing.html ...
Next-generation sequencing (NGS) of the human exome has the potential to identify pathogenic variants responsible for complex phenotypes associated with rare diseases. ...
Gene Panel has been an invaluable tool to analyze parallel gene expression for disease-associated mutations. Next-generation sequencing (NGS) technologies are perhaps the most widely used approaches for gene panel, which can analyze genetic mutations of large sample-size projects and facilitate research on human well-being. https://www.cd-genomics.com/diseasepanel/non-ngs-panel.html ...
NextGENe software is the perfect analytical partner for the analysis of desktop sequencing data produced by Illumina® iSeq, Miniseq, MiSeq, NextSeq, HiSeq, and NovaSeq systems, Ion Torrent Ion GeneStudio S5, PGM, and Proton systems as well as other platforms. NextGENe software runs on a Windows® Operating System, which provides a biologist-friendly ‘point & click’ ...
Since its inception, next-generation sequencing (NGS) has revolutionized genomic research, enabling accelerated biological discoveries and clinical advancements. Its power and application potential as a research tool continues to evolve, driving demand for faster, more accurate sequencers. Built on Ion Torrent™ technology, the Ion GeneStudio™ S5 Systems provide the simplest ...
Next-generation sequencing (NGS) has the potential to revolutionize the diagnosis and treatment of cancers and rare diseases but creates extremely large, complex, and noisy datasets for analysis. Without the right analytical technology, pinpointing causative variants and obtaining actionable insights from NGS data requires specialist skills, multiple resources, and considerable time. The ...
Tempus xE (version 2) is a whole exome next-generation sequencing assay that analyzes the entire coding region (exome) of the patient’s genome, combined with whole transcriptome RNA sequencing. Clinical sequencing is performed to 500x depth of coverage for tumor specimens and 150x for normal specimens for the clinically enhanced regions (648 genes). Non-enhanced regions are performed at ...
ByTempus
The Small RNA Library Prep Kit for Illumina consists of all the reagents and components required to generate small RNA libraries to be used for next-generation sequencing on an Illumina platform. All molecular reagents including adaptors, primers, enzyme mixes and buffers are provided. A purification module is also provided for rapid purification of nucleic acid products generated at various ...
Sequencing-based genome editing validation can detect whether alleles of a gene have been edited correctly, identify insertion and deletion sites at the whole-genome level, and screen and identify monoclonal cell lines. In addition,it is an excellent way to study the off-target effects of CRISPR gene editing. ...