Single-cell RNA sequencing is giving researchers a clearer view of why some CAR-T cells persist, expand, kill tumors ...
Researchers developed STRIPE, a targeted long-read RNA sequencing tool that identifies disease-causing variants missed by ...
Researchers developed a new RNA sequencing strategy that can reveal how genetic variants disrupt gene function and improve the diagnosis of rare diseases. The study team demonstrated that this ...
Pages Latest Report] According to a market research study published by Healthcare Foresights, the demand analysis of Global ...
Researchers updated the global catalogue of human-infective RNA viruses to 239 ICTV-recognised species, incorporating ...
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Mastering sequencing QC for flawless runs
From Illumina to Nanopore to PacBio, getting high-quality sequencing data starts long before the run begins. Careful library prep, accurate quantification, platform-specific QC checks, and novel RNA ...
A comprehensive review article titled “Bioinformatics perspectives on transcriptomics: A comprehensive review of bulk and single-cell RNA sequencing analyses,” published in Quantitative Biology, ...
Plasmidsaurus has launched a new RNA-Seq service for Illumina short read applications, bringing the same approach they use for plasmid sequencing to gene expression analysis. Attendees at this week’s ...
Two new technologies—an AI diagnostic system called DeepRare and a targeted long-read RNA sequencing platform named STRIPE—are showing promise in diagnosing rare diseases that evade standard tests.
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