Ripseq pathogen ID
            Ripseq sequence-based analysis reduces the time needed to identify infectious pathogens, in pure- or poly-microbial samples, by up to 90% - and provides answers where other methods fail. Use any sequencing technology you want - Sanger and Targeted NGS
        
        Click here for a free, unlimited use 14-days trial!
         
        
            
            
                
                    Platform agnostic
                    
                        Ripseq can analyze both NGS & Sanger direct-from-specimen sequencing files. Using
                    our novel algorithms, the total time for one analysis is less than five minutes
                    - no matter if the sample is a negative, pure or a poly microbial one.
                    
                 
                
                
                    Curated databases
                    
                        Our Ripseq DB databases has the most up to date references, but without the clutter.
                    Databases are filtered and automatically curated to ensure an ID you can rely on.
                    
                 
                
                
                    Cloud SaaS solution
                    
                        Ripseq is always online and always updated. All you need is an internet browser.
                    We push our new algorithms as well as new database references up to the cloud every
                    night for your benefit.
                    
                 
                
             
            
            
            
            
                
                    Ripseq NGS - It is FAST!
                    
                        Using our novel algorithms Ripseq will process your targeted NGS sequence file locally,
                    and reduce the information needed to upload by a factor of 1000:1, while still retaining
                    resolution and specificity. This means no lengthy file upload, and no costly big
                    data file storage.
                    
                    
                        After upload, the cloud based Ripseq will analyze the uploaded reads against any
                    of our curated Ripseq DB databases - no matter the target.
                    
                    
                        All this in less than 5 minutes! Including reporting!
                    
                 
                
             
            
            
                
                    Ripseq Sanger - Mono AND polymicrobial samples!
                    
                        Our Ripseq Sanger products can handle it all. No matter if you have a pure sample,
                    or you have a more complex sample (or InDel) resulting in a mixed chromatogram - Ripseq got
                    your back.
                    
                    
                        Using our bulk analysis you can save a lot of time on your pure samples - with bulk
                    upload, bulk analysis, automatic confidence status flags and automatic report generation.
                    No need to sift through hundreds of references in GenBank.
                    
                    
                        Ripseq can also analyze samples you otherwise would have to discard or at best culture
                    and separate, not knowing if you missed anything.
                    
                 
                
             
            
            
                
                    Ripseq DB - The best microbial database there is.
                    
                        Pathogenomix's curated pathogen database Ripseq DB, extends and improves the effectiveness
                    of the public DNA sequence databases such as GenBank and others. While GenBank contains
                    large numbers of current references, it also has many uninformative or even erroneous
                    references that hinder accurate identification.
                    
                    
                        To ensure the best reference quality and accuracy, Ripseq DB enables users to
                    curate a more medically-relevant reference database. Users can annotate, reject
                    and approve references using personalized methods. This on top of the solid foundation
                    of advanced automatic filters and cross referencing makes Ripseq DB the database of
                    choice.
                    
                    
                        Curated databases are a prerequisite for rapid, accurate analysis of Next Generation
                    Sequencing (NGS) as well as Sanger data. This will ensure that the user can be confident
                    that the analysis results are complete and accurate.
                    
                 
                
             
         
        
        
        
        
        
        
        
        
        
        
    
    
        Rapid Direct Sequencing Analysis of Clinical Samples using NGS or Sanger. Less than 5 minutes analysis time. No bioinformatics resources needed. 
Long-read sequencing, long-read analysis, long-read preprocessor, nanopore, Direct Sequencing analysis, identification, mixed clinical samples, patient, dual loci, HLA, HIV, HPV, bacteria, bacterium, fungi, fungal, virus, Sanger, NGS, Ion, Torrent, Illumina, 16s gene, rpob gene, ITS, ITS2 gene, 16s metagenomics, metagenomic sequencing, amplicon, metagenomic sequencing, dna sequencing, fungal sequencing, isentio, bacterial, sequencing, metagenomic, metagenomics, nucleotide sequence, pathogenomix, pathoseq, pathongs, polymicrobial, sequencing, ripseq, rpob sequencing, second opinion, shotgun, metagenomics, targeted ngs, ngs sequencing, full metagenomic sequencing, amplicon