DNAnexus Platform Demo Request DNAnexus helps advance medical discovery by bringing genomic, multi-omics, and clinical data securely together on a single scalable platform.

Accelerate your population-scale research using our suite of intuitive and robust cohort analytics tools. Request a demo today: dnanexus.com/demo-request

#PopulationHealth #Genomics #Multiomics #SomaticVariants #GeneExpression #CohortAnalytics

Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic. #SomaticVariants #ShortReads #LongReads #VariantCalling #Genomics #Bioinformatics #ToolsBenchmarking #ReferenceDatasets @natbiotech.nature.com 🧬 🖥️
www.nature.com/articles/s41...

Practical Somatic Variant Analysis in Cancer Genomics 27-29 April 2026

🚀 Learn somatic variant analysis in cancer genomics! Hands-on online workshop: QC, GATK4 Mutect2, R & VEP annotation. Go from raw data to actionable insights. 🧬📊27-29 April 2026

www.physalia-courses.org/courses-work...

#CancerGenomics #SomaticVariants #Bioinformatics #PrecisionOncology #RStats

A recurrent sequencing artifact on Illumina sequencers with two-color fluorescent dye chemistry and its impact on somatic variant detection. #ShortRead #Sequencing #TwoColorSequencing #SomaticVariants @biorxivpreprint.bsky.social
www.biorxiv.org/content/10.1...

Source: https://www.biorxiv.org/content/10.1101/2024.12.02.625685v1.full.pdf

A robust benchmark for detecting low-frequency variants in the HG002 Genome In A Bottle NIST reference material. #LowFrequencyVariants #SomaticMosaicism #SomaticVariants #VariantCalling #ReferenceMaterials #GiAB #Benchmarking #Genomics 🧬 🖥️ @biorxivpreprint.bsky.social
www.biorxiv.org/content/10.1...