Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • SoftGenetics
    Registered Vendor
    • Apr 2009
    • 36

    Variant Confidence Scoring System added to NextGENe software

    April 15, 2010, State College PA SoftGenetics announced the addition of a unique variant scoring system to its NextGENe software to assist researchers and clinicians utilizing Next Generation sequencing. The novel scoring system provides a confidence scoring based upon multiple factors such as depth of coverage, directionality balance, homopolymer presence as well as sequence direction with greater weighting being given to the 5’ end of the sequence.

    The new NextGENe scoring system is applicable to sequences generated by all major 2nd generation platforms, Illumina GA, Roche Titanium GS as well as the AB SOLiD System.

    “ When analyzing next-generation sequencing data” stated John McGuigan, Biologist at SoftGenetics, “there are many variables that affect the accuracy of mutation calls. The level of coverage, the fraction of reads with the mutation, and the fraction of reads aligned in the forward or reverse direction are always important. The possibility of misalignment as well as potential homopolymer errors in pyrosequencing data also need to be considered. This can be overwhelming for large alignments that may generate thousands of potential mutations. Considering multiple sources of error at once and generating an overall quality measurement is more useful than considering several aspects individually in an all-or-nothing mutation filter. It allows for increased specificity without reducing the sensitivity.”

    NextGENe software, is a free standing, biologist-friendly Windows based analysis tool, requires no scripting, provides analysis modules for all typical applications and is compatible with data from all major 2nd generation sequencing platforms.

    The company offers 30-day trials and no cost web-based training on its genetic analysis software packages. Interested parties may request the software on the company website: www.softgenetics.com or via email: [email protected].

    # #

    SoftGenetics, LLC specializes in the development of genetic analysis tools for both research and diagnostic applications. Hallmarks of SoftGenetics software tools are advanced technologies, providing exceptional accuracy, and sensitivity in an easy-to use Windows® user interface.

    Trademarks are property of their respective owners.

Latest Articles

Collapse

  • SEQadmin2
    Advanced Sequencing Platforms Tackle Neuroscience’s Toughest Genomics Problems
    by SEQadmin2



    Genomics studies in neuroscience face a special challenge due to the brain’s complexity and scarcity of samples. Mapping changes in cell type and state using conventional next-generation sequencing methods remains challenging. Advances in technologies like single-cell sequencing, spatial transcriptomics, and long-read sequencing have opened the door to deeper studies of the brain and diseases like Alzheimer’s, amyotrophic lateral sclerosis (ALS), and schizophrenia.
    ...
    07-09-2026, 11:10 AM
  • SEQadmin2
    Cancer Drug Resistance: The Lingering Barrier to Rising Survival
    by SEQadmin2



    Cancer survival rates have significantly increased in the last few decades in the United States, reaching a combined 70% 5-year survival rate by 2021. Behind this number, there are years of research to find new therapies, drug targets, and early detection methods. But there is one core challenge that keeps slowing down these advances, and it’s about drug resistance.

    There is no single reason why many patients don’t respond to treatment as expected. Cancer is...
    07-08-2026, 05:17 AM
  • GATTACAT
    Reply to Nine Things a Sample Prep Scientist Thinks About Before Sequencing
    by GATTACAT
    Love this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
    07-01-2026, 11:43 AM

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, 07-13-2026, 10:26 AM
0 responses
28 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-09-2026, 10:04 AM
0 responses
37 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-08-2026, 10:08 AM
0 responses
25 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 07-07-2026, 11:05 AM
0 responses
35 views
0 reactions
Last Post SEQadmin2  
Working...