Parse Biosciences

Webinars

Using Single Cell Sequencing to Investigate Murine COVID-19 Mortality

Using Single Cell Sequencing to Investigate Murine COVID-19 Mortality

With flexible and scalable solutions available, learn why single-cell sequencing studies are no longer out of reach. Watch the webinar recording where our speaker, Dr. Benjamin Ostendorf, Charité-Universitätsmedizin, Berlin, presents the results of his recent single-cell study, published Sep 2022 in the Journal Nature, on the role of APOE in Murine COVID-19 mortality.
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Expanding Single Cell Capabilities with Immune Profiling and Targeted Gene Capture

Expanding Single Cell Capabilities with Immune Profiling and Targeted Gene Capture

In this webinar, you will learn about Evercode TCR for immune profiling and Gene Capture for even greater scalability. You will also learn more about Parse's foundational technology platform, which enables single cell RNA sequencing with no microfluidics instrument required.
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Using Single Cell RNA Sequencing (scRNA-Seq) to Examine What Makes Cancer Possible

Using Single Cell RNA Sequencing (scRNA-Seq) to Examine What Makes Cancer Possible

In this webinar, Dr. Katerina Gurova, Roswell Park Cancer Institute, describes how she used scRNA-Seq to examine whether the transition between one epigenetic state into another makes cells vulnerable to oncogene induced transformation.
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High Sensitivity Single Cell RNA Sequencing with Evercode Whole Transcriptome v2

High Sensitivity Single Cell RNA Sequencing with Evercode Whole Transcriptome v2

Single cell RNA sequencing has become a core tool for researchers to understand biology. As scRNA-seq has become more ubiquitous, many applications demand higher scalability and sensitivity. To meet this need, we developed the Evercode Whole Transcriptome v2 solution, a combinatorial barcoding workflow for scRNA-seq with dramatically improved sensitivity, robustness, and unbiased gene expression.
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Single-cell Transcriptomic Landscape in Alzheimer's Disease

Single-cell Transcriptomic Landscape in Alzheimer's Disease

The gene-regulatory landscape of the brain is highly dynamic in health and disease, coordinating a menagerie of biological processes across distinct cell types. Understanding these regulatory programs requires a holistic experimental and analytical approach. Here, we present a single-cell study of 380,000 nuclei in late-stage Alzheimer’s Disease (AD) using parse biosciences whole transcriptome kit, profiling gene expression in thousands of genes and uncovering vast neuronal and glial heterogeneity in late-stage AD.
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Mapping and Modeling the Genomic Basis of Differential RNA Isoform Expression at Single-cell Resolution

Mapping and Modeling the Genomic Basis of Differential RNA Isoform Expression at Single-cell Resolution

In this informative webinar recording, Elisabeth Rebboah, UC Irvine, discusses overcoming these obstacles to perform differential RNA isoform expression at single-cell resolution using the split pool combinatorial barcoding protocol from Parse Biosciences along with a combination of short read sequencing to characterize cell types and long read sequencing to reveal full-length isoforms.
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Single Cell RNA-Seq on the Frontlines: High Multiplex and Time-course Experiments Expand Utility

Single Cell RNA-Seq on the Frontlines: High Multiplex and Time-course Experiments Expand Utility

Experimental designs are growing alongside the increased throughput requirements of single-cell RNA-Seq assays. Replicates, disease states, and time-course designs dramatically increase the number of samples and the burden of information gleaned from a single experiment. Alongside these considerations is a substantial increase in the implications of the results. Our speakers discuss the ramifications of higher-order studies on needs for data quality, throughput attenuation, and sample longevity.
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