Lab Informatics Products & Reviews

Acquire, Analyze & Manage Mass Spectrometry Information in the clinical laboratory

waters_connect is an informatics platform that helps analytical labs, their scientists, and extended ecosystem explore, discover, and push the boundaries of how laboratories use information.

The Waters IdentityE High Definition Proteomics system defines the new standard for rigorous protein identification. The IdentityE High Definition Proteomics System is an UltraPerformance LC® (UPLC)/High-Bandwidth Mass Spectrometry (MS E) system solution suitable for confident protein identification designed to meet stringent requirements as outlined by leading scientific journals.The new Waters IdentityE High Definition Pro…

The Waters OpenLynx™ Open Access Application Manager provides walk-up access for LC/UV, LC/MS, LC/MS/MS, and GC/MS operation in laboratories whose chemists have varying levels of instrumental analysis experience. OpenLynx also provides customizable batch processing to support the large amounts of data generated by high-throughput analyses. It comes standard with MassLynx™ Software. Features of Waters OpenLynx: Easy to Learn T…

Experience seamless connectivity with the Precellys Connect mobile app, enabling Bluetooth wireless integration between your smartphone and the advanced Precellys Evolution Touch tissue homogenizer. Effortlessly monitor and manage your instrument remotely, access protocol databases, and transfer protocols directly from your phone.

CDD Vault is a hosted informatics software that enables researchers to intuitively organize and analyze both biological and chemical data, and to collaborate with partners anywhere in the world through a secure web interface.

Disease, assay, instrument, and site-agnostic. Our end-to-end analysis and reporting solution streamlines your workflow from run and case level QA/QC review to rapid interpretation of NGS testing results, therapy selection, and clinical trial matching, so you can deliver the most precise medical management at every step of your patient’s journey.

REMISOL Advance is a leading middleware solution for today’s clinical laboratories, bridging laboratory information systems (LIS) and instrumentation. It helps drive improved operational efficiency within and across the laboratory network through process automation and standardization.

In-depth understanding of complete genome in human, aninal, plant and microbe with end-to-end services.  

Sequencing only service for customer-premade libraries at different read lengths and capacities to suit any cost, project scale and turnaround with the world-leading, powerful, and sophisticated sequencing platforms (Illumina, Pacbio, and Oxford Nanopore). 

16S/18S/ITS rRNA amplicon metagenomic sequencing employs universal primers to target specific regions to identify the phylogeny and taxonomy from complex microbiomes.

Single cell RNA sequencing uncovers the complexity of cellular diversity to employ the study of unusual cell types, cell-lineage associations, and samples of heterogeneous nature with 10x Genomics technology.

Long Read Sequencing (LRS) service employs cutting-edge technologies such as Oxford Nanopore and PacBio platforms for decoding complex genomes, completing transcriptomes, exploring metagenomes, and investigating structural variations with unmatched precision.  

RNA sequencing is applied for in-depth analysis of whole transcriptomes, encompasses coding and non-coding RNAs (long ncRNA, small RNA, and circle RNA,etc.) for diverse research needs.  

Whole exome sequencing allows for sequencing human and mouse exomes in an array of panel options, which facilitates research contexts and clinical contexts.

Shotgun metagenomic sequencing is designated to sequence the total genomic DNA from environmental samples without the prior isolation and cultivation of individual species. The services are applied for studying the rich genetic repertoire of microbial communities with taxonomy information, and for studying system evolution, gene function, and metabolic network of environmental microorganisms.

Novogene provides Whole Genome Bisulfite Sequencing (WGBS), Reduced Representation Bisulfite Sequencing (RRBS), Chromatin Immunoprecipitation Sequencing (ChIP-seq), RNA Immunoprecipitation Sequencing (RIP-seq), and Assay for Transposase-Accessible Chromatin Sequencing (ATAC-seq), tailored for both bulk and single-cell samples.

Enable seamless communication between computational and medicinal chemists, and with partnering organizations such as CROs

Flare™ is a ligand-based and structure-based drug design platform. Through high-resolution 3D visualization and in-depth analysis of target structures and potential ligands, Flare enables users to optimize and prioritize new molecules efficiently and effectively.

Flare™ enables the production of high-resolution 3D graphics of your ligands and proteins for publications and communication of results.

Flare™ FEP enables research chemists to refine docking results, making the right structure-based design choices for lead optimization with confidence.

Spark™ is a powerful scaffold hopping and bioisosteric replacement solution that generates highly innovative ideas for your project to explore chemical space and escape IP and toxicity traps.

Blaze™ is an advanced virtual screening platform enabling you to dramatically increase your wet screening hit rate at a fraction of the cost.

Cresset Discovery is a premier computational chemistry CRO with a proven track record delivering high impact drug discovery projects. From ideation to synthesis and biological results, their expert CADD scientists are the best at what they do. Working alongside you from the ground up, they apply the best in silico techniques, and give expert advice and guidance, to accelerate your assets through the pipeline.