There's still time to apply for the Omics Discovery Grant from Zymo Research! With 10 days remaining, this is your chance to leverage innovative tools to propel your research. Up to ten research proposals will be awarded the Omics Discovery Grant, which includes: • A Zymo-Seq RiboFree Total RNA Library Kit featuring our universal rRNA depletion technology • Illumina platform paired-end sequencing (at least 30 million paired-end reads per library) • RNA-Seq data analysis and visualization through the Aladdin Bioinformatics Platform, an official partner of Zymo Research • An additional $2,000 credit for RNA-Seq sample prep technologies Plus, all applicants will receive a special offer! Share this post with a colleague and click the link to apply today: https://lnkd.in/gaWzng8V #RNASeq #NGS #RNA #RNAAnalysis #NGSLibraryPrep #Transcriptomics #Microbiomics #Omics #ResearchGrant
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Bioinformatics Grad Specializing in NGS & ML | Ex-BDM @OMC Medical UK | President Luddy Journal Club | Graduate Ambassador
Bioinformatics is an interdisciplinary science integrating genomics, transcriptomics, proteomics, and other omics data to drive innovation in drug discovery. Let's embrace this revolutionary approach to develop more effective and safer drugs for the future. Here is how Bioinformatics contributes to drug discovery. #drugdiscovery #bioinformatics #aiinbioinformatics
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Panashe Nyengera serves as a Bioinformatics Assistant for UGenome. She is pursuing her B.S. in Biotechnology and Bioinformatics, eager to explore new avenues within Bioinformatics and contribute to advancements in genomics research. Panashe is passionate about leveraging data-driven insights to advance precision medicine and drive breakthroughs in bioinformatics research. UGenome is lucky to have her part of the UGenome network. #ugenome, #ugenomeai, #pharmacogenomics, #pharmacogenetics, #bioinformatics, #genetics, #dna, #research, #genomics, #medicine, #drugdiscovery, #datascience, #biostatistics, #pharma, #genomicmedicine, #sequencing, #dataanalysis, #precisionmedicine
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If you are interested in long read sequencing, hear what some Revio users are able to achieve. Many thanks to these LongPlex customers in the webinar for helping us develop the kit.
Join us on October 8th for the virtual launch of our LongPlex Long Fragment Multiplexing Kit, designed to realize the full throughput potential of PacBio long-read sequencers! Register today to gain insights from early users and learn about LongPlex's diverse applications. Sessions include: Long-Read Low-Pass Sequencing: Unveiling the next generation of variant detection Kendall Lee, PhD Co-Founder of Veil Genomics 11:55-12:15 pm ET Recovery & load balancing of long read seq. on difficult bacteria and yeast samples Collin Kessler, PhD Team Lead of Bioinformatics at SeqCenter 12:15-12:35 pm ET Handling the comPlex with LongPlex: Long-read seq. of eukaryotes and metagenomes Dario Copetti, PhD Associate Director of the Arizona Genomics Institute at the University of Arizona 12:35-12:55 pm ET Don’t miss this opportunity to be at the forefront of genomic innovation. #LongPlex #Genomics https://hubs.ly/Q02RlP520
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Assembling complete genomes directly from metagenomes is now a reality! Zymo Research has introduced its Metagenome Assembly Service, leveraging the advanced capabilities of PacBio HiFi sequencing. By harnessing the power of long-read sequencing and sophisticated bioinformatics tools, this innovative service enables researchers to meticulously analyze and reconstruct metagenomes from accurately assembled genomes or genome bins. This development significantly enhances the comprehension of metagenomes, thereby boosting the pace of scientific discoveries. “The application of long-read sequencing in metagenome assembly signifies a milestone within the field of metagenomics. Zymo Research takes great pride in pioneering this service for the benefit of the entire microbiology community. This service allows researchers to focus on scientific discovery, liberating them from the complexities of wet-lab tasks and intricate bioinformatics algorithms in metagenomics workflows." Dr. Shuiquan Tang, Director of Microbiomics at Zymo Research. Read the press release: https://lnkd.in/gizBcCF4 Learn more about Zymo Research's Metagenome Assembly Analysis Service: https://lnkd.in/g6etR8RC ------ #Metagenomics #NGS #Microbiome #Microbiology #Biotech #LifeScience
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Did you know BioIVT screens around 600 new #biospecimens with next-generation #sequencing (NGS) data every month? So even if you’ve searched our inventory for the mutation cohort you need in the past, we may have it now. Our growing collection of screened samples enables you to unlock progress in your research with biospecimens targeted to your specific research needs. Connect now for a custom-tailored inventory report: https://lnkd.in/etjX7wcA Additionally, we can combine our expertise in biospecimen procurement and selection, sample preparation and project management with in-house NGS capabilities to offer both standard and custom services for extraction, library preparation, sequencing and bioinformatics. Learn more: https://lnkd.in/eFedSTeg #mutations #diagnostics #biomarkers #bioinformatics
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If you're getting started with #spatial #transcriptomics and want to understand the technologies and data analysis approaches available out there register for this free webinar!! 💥
Our new webinar series on the advances in spatial omics kicks off next week! Join us for the opening webinar of the series to discover the latest technological advances and computational approaches for analysing spatially-resolved transcriptomics data. Registration is free but essential: https://lnkd.in/ef5mhmXK Speaker: Valentina Lorenzi EMBL European Bioinformatics Institute | EMBL-EBI #bioinformatics #datascience #computationalbiology #omics #multiomics #transcriptomics #singlecell #genomics #spatialomics
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What an interesting service and/or an application with single cell biology: - What if you can a single-cell Whole Genome Sequence (WGS)? - What if you get this single-cell WGS from one cancer cell and the other normal cell nearby? - What if you can get at 100x for each cell with a reasonable low cost? >>> My thought is to think about a case for this application of scWGS - can we use this for the needle biopsy analysis? If we only get a few cell as an earlier screening or diagnostic step, if we have a few cells from fine-needle biopsy, with this method, we may be able to confirm if the tumor-like cell has the somatic mutation compared with the normal cells. >>> we shall rank this is a good application enabled by lowering the sequencing cost … to confirm the cancerous cell from fine-needle biopsy. #single-cell, #WGS, #scWGS, #biopys and #NGS
#Mirxes has launched our new research service - Single-cell Whole Genome Sequencing (scWGS). With scWGS, you can confidently capture somatic mosaicism at the single-cell level and unravel cell lineage. Our scWGS service offers: - Exceptional Whole Genome Amplification performance (high genome coverage, low amplification error and reduced artifacts) - End-to-end service (Sample preparation, Sequencing and Bioinformatics analysis) - Expert Bioinformatics support (CNV, SNV, indel analyses etc) Explore our cutting-edge scWGS service today: https://lnkd.in/gDEzKA4M #preventivehealthcare #precisionmedicine #biotech #researchanddevelopment #earlydetection #earlydetectionsaveslives #healthcare #cancerearlydetection #RNA #research #Genomics #singlecell #sequencing
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Bioinformatics is an interdisciplinary science integrating genomics, transcriptomics, proteomics, and other omics data to drive innovation in drug discovery. Let's embrace this revolutionary approach to develop more effective and safer drugs for the future. Here is how Bioinformatics contributes to drug discovery. hashtag #drugdiscovery hashtag #bioinformatics hashtag #aiinbioinformatics Your document has finished loading
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"Excited to present our latest research paper titled 'Analysis of Differentially Expressed Mycobacterium Fortuitum Proteins for Biomarkers Using Support Vector Machine,' accepted at ICIIP and published in IEEE. Delving deep into bioinformatics, this study explores new avenues for biomarker discovery. #Bioinformatics #ICIIP #IEEE #ResearchPaper #Biomarkers"
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A Game-Changer in Bioinformatics! Our latest article on Newzchain delves into how PipeBio is revolutionizing the field by providing scientists with a powerful #cloud-based platform for bioinformatics analysis. PipeBio’s platform is tailored to meet the complex needs of modern biological research, offering robust tools that enhance the ability to analyze and interpret biological data effectively. Backed by Y Combinator, their service facilitates groundbreaking discoveries in genomics, proteomics, and other critical areas of biotechnology by simplifying the computational challenges that researchers face daily. Read the full article here: https://lnkd.in/gaBfknCf #Bioinformatics #Biotech #CloudComputing #ScientificResearch #PipeBio #Genomics #Proteomics #Newzchain
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