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🚀 Accelerate Your RNA-seq Data Analysis! 🚀 Say goodbye to long wait times and hello to rapid insights with our RNA-seq Analysis Portal. Process your valuable RNA-seq data in hours instead of days and perform your analyses anytime, anywhere. 🌍 🔬 Key Features: - Fast Processing: Go from FASTQ files to pathway analysis insights in hours. - Broad Compatibility: Supports 20 species and works with major RNA library kits. - Seamless Integration: Push data directly to your IPA account for biological interpretation. Don’t let data analysis slow you down. Start working with your data faster and more efficiently today! https://lnkd.in/dAnPFHHR #RNAseq #DataAnalysis #Bioinformatics #GeneExpression #NGS

🧬 Excited to share my latest video on RNA-Seq Introduction! 🧬 Are you curious about the cutting-edge technology revolutionizing gene expression analysis? Look no further! I've created an introduction to RNA-Seq that breaks down this complex topic into easy-to-understand concepts. In this video, you'll learn: • What RNA-Seq is and why it's important • How RNA-Seq compares to traditional methods • The basic workflow of an RNA-Seq experiment • Key applications in research and medicine Whether you're a student, researcher, or just passionate about genomics, this video will provide valuable insights into the world of RNA sequencing. 🎥 Watch it here: https://lnkd.in/euDwcex7 Don't forget to like, subscribe, and share if you find it helpful! Let's spread knowledge and foster scientific understanding together. #NGS #RNASeq #Genomics #Bioinformatics

For anyone familiar with Golden Helix bioinformatic tools, especially VarSeq, you may assume our pharmacogenomics capabilities are limited to sequencing data only. Fortunately, that isn't the case and we are more than comfortable helping your lab deploy a complete PGx workflow using your current array data.

Check out a small case study Gillian Belbin performed at Gencove involving assessing the utility of WES data for whole genome imputation! tl;dr is that it works super well https://lnkd.in/gnsw5rM4

𝐓𝐫𝐚𝐧𝐬𝐟𝐨𝐫𝐦 𝐘𝐨𝐮𝐫 𝐑𝐞𝐬𝐞𝐚𝐫𝐜𝐡 𝐰𝐢𝐭𝐡 EditCo Bio 𝐏𝐫𝐞𝐜𝐢𝐬𝐢𝐨𝐧 𝐀𝐫𝐫𝐚𝐲𝐞𝐝 𝐂𝐑𝐈𝐒𝐏𝐑 𝐠𝐑𝐍𝐀 𝐋𝐢𝐛𝐫𝐚𝐫𝐢𝐞𝐬 Maximize your genomic research potential with EditCo Bio's Arrayed CRISPR gRNA Libraries. Engineered using our advanced multi-guide technology and superior synthetic sgRNAs, these libraries offer targeted gene editing in a precise multi-well plate format, significantly increasing the likelihood of achieving functional knockouts. 𝐄𝐱𝐜𝐞𝐩𝐭𝐢𝐨𝐧𝐚𝐥 𝐊𝐧𝐨𝐜𝐤𝐨𝐮𝐭 𝐄𝐟𝐟𝐢𝐜𝐢𝐞𝐧𝐜𝐲: Benefit from our rigorously tested multi-guide strategy that guarantees functional knockouts with high specificity. 𝐒𝐭𝐫𝐢𝐧𝐠𝐞𝐧𝐭 𝐐𝐮𝐚𝐥𝐢𝐭𝐲 𝐂𝐨𝐧𝐭𝐫𝐨𝐥: Our libraries undergo stringent quality checks to ensure high precision and reliability, providing consistent results across your CRISPR screens. 𝐀𝐜𝐜𝐞𝐥𝐞𝐫𝐚𝐭𝐞𝐝 𝐃𝐞𝐥𝐢𝐯𝐞𝐫𝐲 𝐓𝐢𝐦𝐞𝐬: Our streamlined production process delivers your custom CRISPR libraries within just 7 days, expediting your path from concept to experimentation. 𝐄𝐟𝐟𝐢𝐜𝐢𝐞𝐧𝐭 𝐃𝐚𝐭𝐚 𝐀𝐧𝐚𝐥𝐲𝐬𝐢𝐬: Avoid the complexity of NGS with our Inference of CRISPR Edits (ICE) platform, enabling quick analysis of CRISPR edits via Sanger sequencing. 𝐄𝐱𝐩𝐥𝐨𝐫𝐞 𝐈𝐂𝐄 𝐟𝐮𝐫𝐭𝐡𝐞𝐫 👉 https://lnkd.in/gZDPvevg 👈 𝐄𝐱𝐩𝐥𝐨𝐫𝐞 𝐀𝐫𝐫𝐚𝐲𝐞𝐝 𝐬𝐠𝐑𝐍𝐀 𝐋𝐢𝐛𝐫𝐚𝐫𝐢𝐞𝐬 👉 https://lnkd.in/gvJZqsDt 👈 Empower your research with EditCo Bio innovative CRISPR solutions that set new standards for precision and efficiency in genetic research. Our technologies are designed to accelerate your discoveries, from initial screening to clinical applications. EditCo Bio 𝒊𝒔 𝒆𝒂𝒈𝒆𝒓 𝒕𝒐 𝒔𝒖𝒑𝒑𝒐𝒓𝒕 𝒚𝒐𝒖𝒓 𝑪𝑹𝑰𝑺𝑷𝑹 𝒔𝒄𝒓𝒆𝒆𝒏𝒊𝒏𝒈 𝒑𝒓𝒐𝒋𝒆𝒄𝒕𝒔. 𝑺𝒉𝒂𝒓𝒆 𝒚𝒐𝒖𝒓 𝒑𝒓𝒐𝒋𝒆𝒄𝒕 𝒅𝒆𝒕𝒂𝒊𝒍𝒔 𝒘𝒊𝒕𝒉 𝒖𝒔, 𝒂𝒏𝒅 𝒍𝒆𝒕’𝒔 𝒂𝒅𝒗𝒂𝒏𝒄𝒆 𝒚𝒐𝒖𝒓 𝒓𝒆𝒔𝒆𝒂𝒓𝒄𝒉 𝒕𝒐𝒈𝒆𝒕𝒉𝒆𝒓. #CRISPRScreenSmarter #CRISPRLibraries #EditCoBio #EditCo #GenomeEngineering #BiotechInnovation #ArrayCRISPRLibrary #Genetics #CRISPR #Cas9 #Bioinformatics #MachineLearning

Our review paper highlighting unity amongst the diverse classes and types of CRISPR-Cas systems. Chhandosee Ganguly, Saadi Rostami, Kole Long

Discover the profound influence of epigenetics, genetics, and the APOE gene on Alzheimer's disease in our latest blog. Knowledge is key in the battle against this formidable condition. Alzheimer's remains a paramount challenge, impacting lives and demanding innovative solutions. Our recent article, "New Insight into How APOE4 Drives Alzheimer's," sheds light on the significant role of the APOE gene, emphasizing the critical importance of understanding your genetic data. Knowledge is a powerful tool in the fight against Alzheimer's. Understanding your genetic data empowers you to make informed decisions, take preventive measures, and contribute to ongoing research. Together, we move closer to a future where Alzheimer's is treatable or preventable. 🔗 Read the full blog: https://lnkd.in/dgAbkir8 #AlzheimersResearch #GenomicHealth #APOEgene #MosaicBiodata #HealthcareInnovation #GeneticInsights

DRAGEN wins at PrecisionFDA Truth Challenge V2 showcase accuracy gains! Leverage industry-leading variant calling accuracy*, with >5.5M genome equivalents analyzed on DRAGEN™ secondary analysis. Find out more: https://ilmn.ly/3WJdV0S

Exciting News! We are thrilled to announce that LOVD annotations are now available in VarSeq for both variants and CNVs! Discover how this new annotation source can enhance your genetic research and provide deeper insights. Dive into our latest blog to learn more! Read the full blog here: https://bit.ly/3KkvAFd #Genomics #Bioinformatics #LOVD #VarSeq #GoldenHelix #GeneticResearch

Join the ever-expanding number of researchers who trust QIAseq NGS technologies. With faster workflows, accurate results and integrated data analysis, once you make the switch to QIAseq, you never look back. Discover the magic of QIAseq. ⬇️