Twist Bioscience’s Post

Improving cfDNA sequencing sensitivity by optimizing library preparation. Explore a cfDNA library preparation workflow that provides high yield and conversion to improve sensitivity and detection of low variant allele frequencies (VAF). Twist Bioscience, #cfDNA, #DNA, #libraryprep

This study by Wang C and Fan X focuses on the advancements in single-cell multi-omics sequencing techniques, particularly their application in understanding the nervous system. The review explores the evolution of single-cell sequencing from transcriptome analysis to multi-omics, enabling a comprehensive view of cellular heterogeneity. Read more 👉 https://lnkd.in/eEJisHxd #SingleCellSequencing #MultiOmics #NeuralResearch #ResearchInsights

Remember When? It's been 6 Months since we started shipping our CosMx Human 6K Discovery Panel, the highest plex available for single-cell spatial research. With the power of plex and the CosMx™ SMI, researchers can answer the most challenging questions and take the leap to single-cell spatial! > Measure 6000 RNA targets 🎯 > Profile significant genes across every biological pathway + over 400 ligand-receptor pairs >Best-in-class cell segmentation What are you waiting for? Get the power of plex today! https://lnkd.in/gyzWzwi8

The 1.5B flow cell is here to give you the flexibility to tackle your smaller batch or pilot projects, sequencing ~4 human genomes, ~41 exomes, or ~30 transcriptomes per flow cell on the #NovaSeqX. #IlluminaProud

Check out our paper about the 10 new HLA alleles we discovered in the past two years! This brings the total of new alleles we discovered to 63 since we started next generation sequencing in 2018. https://lnkd.in/eHSqTfix

The 1.5B flow cell is here to give you the flexibility to tackle your smaller batch or pilot projects, sequencing ~4 human genomes, ~41 exomes, or ~30 transcriptomes per flow cell on the #NovaSeqX. #IlluminaProud

The 1.5B flow cell is here to give you the flexibility to tackle your smaller batch or pilot projects, sequencing ~4 human genomes, ~41 exomes, or ~30 transcriptomes per flow cell on the #NovaSeqX. #IlluminaProud

Optimize data analysis challenges in drug discovery and clinical trials in Next-Generation Sequencing (NGS) with Velsera. Watch the webinar today to address a pivotal pain point in genomics: reference bias. Traditional genomic analysis relies on linear references, which do not accurately represent the diversity of human genomes, particularly for individuals of non-European ancestry. This webinar explores seamless alternatives to help solve reference bias in traditional NGS pipelines, enabling researchers to uncover vital genomic variations that were previously concealed in their data - not only enhancing accuracy in variant calling but also optimizing compute resources, thereby reducing costs and accelerating time-to-result. Watch on-demand today! https://lnkd.in/gKNVtSjm #GRAF #NGS #EraOfVelsera

The 1.5B flow cell is here to give you the flexibility to tackle your smaller batch or pilot projects, sequencing ~4 human genomes, ~41 exomes, and ~30 transcriptomes per flow cell on the #NovaSeqX. #IlluminaProud

Next-Generation Sequencing (NGS) has revolutionized both our understanding and utility of genomics, marked by a surge in direct-to-consumer genomics and transformative therapeutic advancements. As applications and method developments increase, more challenges are also revealed in the NGS landscape. AUGenomics CEO Hannah Dose talks logistical challenges in NGS as a sequencing service provider, and the strategic solutions that save time and resources. Watch the full video: https://lnkd.in/gUhFX6n6 #genomicsequencing #exomesequencing #bioinformatics