Breakthrough Genomics

🧬𝐏𝐫𝐨𝐝𝐮𝐜𝐭 𝐔𝐩𝐝𝐚𝐭𝐞𝐬 𝐈𝐧 𝐎𝐜𝐭𝐨𝐛𝐞𝐫 - 𝐏𝐚𝐫𝐭 𝟏🧬 Universal Sequencing Technology launched TELL-Meta software pipeline for metagenomics applications Ionpath launched MIBIplus an all-in-one, single-cell spatial proteomic solution Bruker released the OptoVolt™ module GeneCentric Therapeutics, Inc. launched EXpressCT liquid biopsy platform CD Genomics launched its comprehensive small RNA sequencing services SeqOne introduces DiagAI Score for genomic data interpretation PacBio introduced SPRQ, an upgraded sequencing chemistry for the Revio™ system Charles River Laboratories launched the Retrogenix® Non-Human Protein Library NewBiologix launches Xcell™ for gene & cell therapy production Geneyx Genomex Ltd. & Ocean Genomics, Inc. launched the SVDuo software Leica Microsystems introduced SpectraPlex, a high-multiplex imaging product on the Stellaris confocal platform for 3D spatial phenotyping Inocras Inc. launched MRDVision which leverages Ultima Genomics ppmSeq technology Creative Proteomics launched innovative Acylcarnitine Analysis Service for metabolic research Twist Bioscience launched its FlexPrep Ultra-High Throughput Library Preparation Kits DNASTAR released Lasergene 18, an update to its Lasergene software package BD launched the BD Omics-One XT WTA Assay whole-transcriptome amplification kit SCIEX introduced the ZenoTOF 7600+ mass spectrometer Parse Biosciences launched its GigaLab, a service offering for large-scale single-cell projects QIAGEN's Digital Insights business has launched Pharmacogenomic Insights (PGXI) 𝗤𝗶𝗮𝗴𝗲𝗻 launched two QiaSymphony kits for extracting ccfDNA from up to 10 ml samples Inagene Diagnostics Inc launched its Cardiovascular Health Test in Canada. Proteintech Genomics has launched the MultiPro Human Discovery Panel for single-cell multiomics Breakthrough Genomics introduced an updated version of its automated genome reader, Virtual Geneticist MagBio Genomics Inc. launched the SFD-10HT kit for separating long and short DNA fragments Golden Helix, Inc. updated VarSeq 2.6.2 software for enhanced pharmacogenomics capabilities NeoGenomics Laboratories introduced AML Express, a rapid NGS assay for genetic profiling in acute myeloid leukemia Curio Bioscience launched Trekker, a single-cell spatial mapping kit that transforms genomics data into tissue-specific spatial information seqWell launched the LongPlex Long Fragment Multiplexing kit Sphere Fluidics Limited launched Cyto-Mine Chroma, the second generation of its flagship Cyto-Mine platform Children's Mercy Kansas City launched the Kiddose PGx test, it's the first paediatric hospital in Missouri to offer in-house pharmacogenetic testing Genomenon, Inc added curated variants for ACMG - American College of Medical Genetics and Genomics secondary findings genes to its Mastermind Professional Edition software platform. LGC Clinical Diagnostics launched Seraseq ctDNA prostate reference materials

Breakthrough Genomics is launching an upgraded version of Virtual Geneticist (VG), its automated genome reader, to revolutionize clinical genomic interpretation and accelerate rare disease diagnosis. Available free, VG aims to make genomic analysis more accessible for clinicians globally. Read more: https://lnkd.in/d8SPEWu3 #BreakthroughGenomics #VirtualGeneticist #GenomicAnalysis #RareDiseases #HealthcareInnovation #Genomics

BREAKTHROUGH GENOMICS is proud to be listed among the Top 10 Contributors of Rare Disease Variants to #ClinVar. We are honored to support the community with over 129,000 variants submitted to this essential database for rare disease diagnosis. National Center for Biotechnology Information (NCBI)