Parse Biosciences
@ParseBio
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Scalable Single Cell Sequencing Without the Instrument | Single Cell Whole Transcriptome Kits | Profile millions of cells
Seattle, WA
Joined May 2018
We're excited to announce a partnership with Codebreaker Labs to combine our technologies to develop and validate a breakthrough platform capable of testing thousands of genetic variants in parallel and measuring their effects at single cell resolution. https://t.co/ykLHYtXU4f
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Register to join our webinar happening next month where our speakers will teach us how to integrate single cell sequencing into Hematology research! https://t.co/1EF32Sm2cI
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The integration of scRNA-seq and AI is reshaping how we study biology and discover therapies. https://t.co/wRmmCleZjz By learning from large perturbation datasets, AI can uncover dysregulated pathways and key regulatory nodes, revealing precise new drug targets.
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We've been having a great time down in Orlando at #ASH25! Thank you to everyone who stopped by the Parse booth to learn more about the newly released Evercode Whole Blood Fixation Workflow for single cell profiling. https://t.co/pOdgqjgOSZ
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How can we advance science ethically without compromising data quality? https://t.co/6bw1q5u5WC We talked with Amy Van Aartsen, researcher and co-founder of the Marty Project, who shared her perspective on the global shift away from animal testing.
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We’re excited to announce the launch of EvercodeWhole Blood Fixation, a new kit that enables immediate stabilization of whole blood at the point of collection for high-quality single cell analysis. https://t.co/vtB0R7w1u9
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Our team will be onsite at Seattle Children's next week for a Lunch & Learn Seminar! https://t.co/6m3tJ96Gqz Join us on December 10th to learn about Evercode single cell technology (now available from the Genomics and Spatial Biology CoLab), Trailmaker demos, and more!
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Ever wondered how birds navigate without GPS and road signs? 🐦 They rely on the Earth’s magnetic field. A new study using scRNA-seq uncovered where this magnetic sense lives in pigeons, and it’s not the eye or the beak as long believed. https://t.co/htmOa59tc6
#singlecell
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With the FDA moving away from mandatory animal testing, researchers are embracing human-based models, like organoids and organ-on-a-chip. Combining these models with high-throughput scRNA‐seq gives unique insight into disease mechanisms & drug response. https://t.co/pyLETE0ONF
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We are thrilled to share the winners of the Parse Evercode Single Cell Grant Program! Congratulations to Caterina De Rosa and Eduardo Guerra Amorim. 🎉 We are so excited to see where your research takes you. Congratulations from all of us at Parse!
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Thank you to everyone who joined our webinar today, and especially to our speaker Dr. Ruslan Rafikov! https://t.co/srE7rbfAiu Dr. Rafikov shared his recent work mapping endothelial heterogeneity and plasticity in the lung using single cell RNA sequencing.
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We're excited to announce the launch of a breakthrough technology that unlocks the full potential of formalin-fixed, paraffin-embedded (FFPE) samples, opening new possibilities for discovery in oncology, translational research, and precision medicine. https://t.co/FK5NdxMlxv
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🌴 Hey San Diego! We'be at #SfN25 starting this weekend and we can't wait to chat with you about how scRNA-seq is advancing neuroscience research. Visit these faces at booth #801! Plus, register for our event happening this Sunday 🧠 https://t.co/QlnZzIES5e
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We're excited to announce a collaboration with Third Rock Ventures to create the largest atlas of 5 million TCRs using the Parse GigaLab, aiming to transform understanding of immune-driven illness and accelerate drug discovery. https://t.co/Xmm0Opaq5R
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On Nov 19th Dr Ruslan Rafikov, Professor of Medicine at Indiana University and Co-founder at Metafora will share his recent work mapping endothelial heterogeneity and plasticity in the lung using single cell RNA sequencing. Register: https://t.co/AalSy7Nrq4
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Our team is at @sitcancer this week! Don't miss our first two poster sessions tomorrow to learn how the Evercode technology is helping researchers use single cell sequencing for cancer immunotherapies.
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Today marks a new chapter for Parse Biosciences as we announce our plans to join QIAGEN. https://t.co/77DWoYhuc7 This partnership strengthens our ability to deliver instrument-free, high-throughput single cell solutions to researchers worldwide.
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How do GLP-1 agonists drive lasting genomic effects? 🤔 Dr. Sam Van de Velde from Salk Institute explored the genomic response to GLP-1 agonists in pancreatic beta cells, revealing PKA-driven phosphorylation of Med14 as a key mediator of sustained genomic response.
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