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  • thezgabby
    Junior Member
    • Feb 2021
    • 2

    End-to-End Bulk RNAseq Analysis on Demand

    Hi everyone,

    Really excited to be a part of this community. I am one of the team members of BioBox Analytics. We're a group of former academics that are building a powerful software platform for scientists working with NGS data that is intuitive and easy to use.

    Our platform is a self-serve data analytics solution that integrates your NGS data with powerful analytics tools. We enable you to analyze and explore your data on demand and accelerate your time to scientific discovery.

    Some features include:
    • Create & run bioinformatic pipelines in the cloud (FASTQC, STAR, DESeq2)
    • Auto-generate interactive visualizations like heatmaps, volcano plots, lollipop plots and scatter plots
    • Connect data directly to public databases to derive relevant insights
    • Leverage a gene search engine to provide in-depth information about your gene of interest and how it relates back to observations within your own datasets.


    Right now, we support human and mouse RNAseq/WGS/WES data, with a focus on gene expression and mutational analysis.

    Visit our website for more information.

    Give it a try, it's free use. Let me know your thoughts - your feedback is how we improve. Appreciate it in advance. Cheers!

Latest Articles

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  • 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

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