We specialize in supporting research teams through every stage of their projects, from securing funding to project/grant development, publishing results and ensuring compliance.
We Process, analyze, and interprete high-throughput sequencing data (e.g., DNA, RNA, whole-genome sequencing) and also Identify genetic variants, SNPs, or structural variations for research and clinical applications.
We predict protein structures using computational modeling tools and also analyze protein-ligand interactions and functional annotation for drug discovery.
We provide RNA-Seq data analysis to identify differentially expressed genes and also pathway enrichment analysis to understand biological mechanisms.
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