Source BioScience’s Post

📢 New post 📢 Are you looking to accurately measure DNA or RNA levels in your samples with unparalleled precision and efficiency? Source Genomics offers cutting-edge qPCR services designed to meet your research needs. Discover more about qPCR by reading our latest post "Enhance Your Research with Source Genomics qPCR Services" here 👉 https://lnkd.in/e2dH6YBj #Genomics #SangerSequencing #NGS #Sequencing #GenomeMapping #Biomarkers #BiomarkerDiscovery #Multiomics #DrugDiscovery #qPCR #TheSequencingPeople #Science #LifeScience

INTEGRA's best PCR purification and NGS size selection solutions! The reliability of #PCRpurification and #NGSsizeselection is paramount in the rapidly evolving field of #genetics and #genomics. Magnetic bead-based methods play a vital role in preparing DNA samples for downstream analysis and ensuring the removal of unwanted contaminants and fragments. Whether your focus is on PCR purification to isolate amplified DNA products, or NGS size selection targeting specific fragment sizes for efficient sequencing, our solutions are tailored to enhance your genomics workflows. Discover which product bundle best suits your laboratory's needs!  Contact us to discuss your application requirements and learn how our tailored solutions can streamline your genomics workflows. #MAGmodules #ASSISTplus #VOYAGER #pipetting #AccelerateScientificDiscovery

INTEGRA's best PCR purification and NGS size selection solutions 😍 The reliability of #PCR purification and #NGS size selection is paramount in the rapidly evolving field of #genetics and #genomics. Magnetic bead-based methods play a vital role in preparing DNA samples for downstream analysis and ensuring the removal of unwanted contaminants and fragments. Whether your focus is on PCR purification to isolate amplified DNA products, or NGS size selection targeting specific fragment sizes for efficient sequencing, our solutions are tailored to enhance your genomics workflows. Discover which product bundle best suits your laboratory's needs! Contact us via DM to discuss your application requirements and learn how our tailored solutions can streamline your genomics workflows. #MAGmodules #ASSISTplus #VOYAGER #pipetting

In this interview, Rami Mehio, head of software and informatics at Illumina, shares his experiences and contributions to major genomic projects like the UK Biobank's whole genome sequencing. He discusses the challenges and innovations in genomic data analysis, highlighting Illumina's role in advancing genetic research and precision medicine. https://lnkd.in/ecMZdvq8 #precisionmedicine #research #genomics #sequencing #wholegenomesequencing #bioinformatics #genetics

Imagine a microscopic game of 'Where's Waldo?' but for genes! Microarray tech puts thousands of DNA probes on a tiny chip allowing simultaneous analysis of thousands of genetic markers. From understanding disease predispositions to unraveling ancestry, revealing genetic mysteries in your samples is a boundless pursuit with microarrays. https://hubs.ly/Q02trKC30 #Biotechnology #ClinicalResearch #Genomics

Discover some of Novogene's services that can be applied to the study of plant and animal microbiomes: Shotgun-based metagenomic sequencing: https://bit.ly/3k7naaB. Amplicon-based metagenomics sequencing: https://bit.ly/3W0SMf5. Metatranscriptomics: https://bit.ly/3X25JXi

Unlock the power of structural variant analysis with our latest blog post! Discover how the Breakends Table in VarSeq simplifies the identification and interpretation of structural variants, making your research more efficient and accurate. Don't miss out on this deep dive into innovative genetic research tools! Read more here: https://bit.ly/3VLrYBn #Genetics #Genomics #StructuralVariants #VarSeq #GoldenHelix #GeneticResearch #Bioinformatics

Source Genomics expands rapid sequencing services 🧬 In addition to whole plasmid nanopore sequencing up to 30kb, you can now easily submit your samples for sequencing of large constructs up to 300kb as well as amplicon sequencing. Discover more about the service here 👉 https://lnkd.in/eNxfNr3C #Genomics #SangerSequencing #NGS #Biomarkers #Olink #Proteomics #BiomarkerDiscovery #DrugDiscovery #Multiomics #Genome #LifeScience #DNA #TheSequencingPeople

🔬 New Development in Single-cell RNAseq! 🧬 Sharing a new tool for scRNAseq demultiplexing detailed in a recent bioRxiv article, "demuxSNP: supervised demultiplexing scRNAseq using cell hashing and SNPs" by Michael P. Lynch, Yufei Wang, Laurent Gatto, and Aedin C. Culhane. 📊 demuxSNP is a supervised algorithm that improves the accuracy of demultiplexing by integrating cell hashing with SNPs. 🔵 Uses genetic variation to train a KNN classifier, enhancing the prediction of demultiplexing classes for cells that are unassigned or of uncertain status. 🟡 Shows better performance over existing methods, particularly in scenarios of low hashing quality or high doublet rates, enabling the recovery of more high-quality RNA cells. 📚 bioRxiv paper: https://buff.ly/4abTQUE 👨💻 R package: https://buff.ly/3UG8JsE 📢 Join the Conversation 📢 Share your ideas, methods, and tools in the comments! 👇 💬 #SingleCell #RNAseq #Genomics #Bioinformatics #demuxSNP #CellHashing #InnovationInScience

If you're at AGBT - Advances in Genome Biology and Technology this year, be sure to stop by poster 514 and learn from Cynthia about our new OMICS-Guard buffer that helps preserve cell viability and RNA/protein integrity for up to 72hr without fixation. No more rushing with those clinical samples, time point collections, tissue harvests, etc.--throw them in the buffer and save your flow, RNAseq/CITEseq, and qPCR experiments for the next day. #singlecellanalysis #multiomics #AGBT2024 #flowcytometry