Neogen Informatics Inc.

Demystifying long-read RNA-seq analysis with FLAIR Learn about FLAIR and its role in transforming transcriptomics through long-read sequencing methods and detailed analysis.

💻 Join our upcoming webinar: Exploratory Single-Cell RNA-Seq Analysis

Are you seeking to maximize the potential of hashtag RNA-Seq analysis?

This webinar will provide you with the essential tools and advanced techniques to transform raw data into meaningful biological insights. Perfect for bioinformaticians and researchers seeking to enhance their analysis capabilities, this session offers a comprehensive exploration of multi-sample scenarios and advanced cell-specific discoveries.

🧬 From Reads to Biological Insights: Single-Cell Transcriptomics Made Easy with hashtag

You can choose between two sessions at different times to fit your schedule!👇

https://events.zoom.us/ev/AgBLSys3clS9Y95IXs5Ccb3s_6MC9zxgNbTZbuCF-l5_0oZBw57N~AiogvZZy4UhJWlpiVP2qwDpiLaQRW-4IPkdm8xBiLq7ouDYf7H35QJENKw

Experience the full potential of 3.1 with our 7-day free trial 👉 www.biobam.com/trial/

You'll get the chance to try the latest analysis pipelines and learn about all the new features. And full access to the complete set of Omicsbox Modules:

🧬Genome Analysis: Easily convert raw DNA-Seq reads into a structurally annotated and curated draft genome.

🧬Genetic Variation: Identify and analyze genetic variations within a population or a species.

🧬Transcriptomics: Convert your RNA-Seq samples into Biological Insights.

🧬Functional Analysis: Functionally annotate and analyze any sequence dataset from scratch.

🧬Metagenomics: Analyze and compare microbiome samples through taxonomic and functional classifications.

From Reads to Insights, fast and easy!

Our website has got a new look with a lot of options. Request a quote directly from our website

Home | Neogen Informatic Inc Renowned bioinformatics company Biobam S.L. recently launched its new complete bioinformatics solution named OmicsBox which has replaced Blast2GO completely. OmicsBox is a bioinformatics software solution that allows getting from reads to insights with ease. Use OmicsBox for the NGS data analysis of...

OmicsBox 3.0 with a new module Genetic Variation.
The Genetic Variation Module allows for performing variant calling, filtering, and annotation, as well as associating genetic variations with a particular trait or disease via genome-wide association studies.