Use Case: Reanalyzing Public RNA-seq Data of IL-17A-Induced Changes in Osteoarthritis Cell Models
April 16, 2025
Reanalyzing public RNA-seq data on IL-17A-induced changes in osteoarthritis cell models using g.nome and OmicsPlayground for streamlined, no-code bioinformatics workflows.
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Case Study: Empowering Single-Cell Research with Expert Bioinformatics Support
February 12, 2025
Empowering single-cell research with Almaden Genomics' bioinformatics support, enabling labs to derive meaningful insights from complex scRNA-seq data.
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News: Almaden Genomics Introduces g.nome® 2.0, a Platform Enhancement to Empower Data Analysis and Interpretation
January 13, 2025
Almaden Genomics has launched g.nome 2.0, enhancing bioinformatics tools with advanced analytics and a streamlined interface for researchers and biologists.
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News: BioNTX Unveils 2024 Rising Stars at the iC³® Life Science & Healthcare Innovation Summit
October 1, 2024
Almaden is recognized among the groundbreaking companies honored as 2024 Rising Stars at the iC³ Life Science & Healthcare Innovation Summit.
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News: Almaden Launches New Data Management and Informatics Service Business
September 17, 2024
Almaden Genomics has launched a new Data Management and Informatics Services business to support its bioinformatics and computational biology solutions.
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Use Case: End-to-End Analysis for Colorectal Cancer RNA-seq Data
August 8, 2024
Explore the insights gained from re-analyzing colorectal cancer RNA-seq data using the Almaden Genomics g.nome platform.
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Webinar: Bulk RNA-Seq Analysis for Biomarker Discovery
August 7, 2024
Explore biomarker discovery through bulk RNA-Seq analysis in this webinar. Learn how to simplify RNASeq analysis, assess quality, and identify biomarkers with the g.nome® platform.
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Use Case: Survival Analysis of Colorectal Cancer Patients
July 2, 2024
Explore how survival analysis of colorectal cancer patients using g.nome reveals prognostic biomarkers and genetic markers impacting patient outcomes, offering insights into personalized treatment.
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Blog: Revolutionizing Genomics: Accurate Genotype Imputation for Rare Variants
June 20, 2024
Discover how Selphi, a novel genotype imputation method by SelfDecode, revolutionizes genomics research with superior accuracy in detecting rare genetic variants.
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