Decima predicts gene expression at single-cell resolution
RNA sequencing from more than 22 million cells trained a model that predicts cell-type-specific gene expression and noncoding variant...
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RNA sequencing from more than 22 million cells trained a model that predicts cell-type-specific gene expression and noncoding variant...
RNA sequencing with regRNA Capture-seq identified thousands of regulatory RNAs and enabled new strategies to increase expression of disease-related genes using ASOs...
by Andrea Repele, Joanna Handzlik, Nimasha Samarawickrama, Trevor Long, Sunil Nooti, Veena Potluri, Yen Lee Loh, Manu The differentiation of hematopoietic progenitors into special...
CIPHER‑seq is a single‑cell method that measures RNA and proteins simultaneously, exposing gaps in cytokine signaling and reducing mitochondrial stress signatures to give a clearer...
RNA sequencing calibration using standardized references enables absolute quantification of gene expression, improving cross-study comparisons and reducing bias across experiments...
The collaboration brings together OneCyte's proprietary single-cell platform for high-throughput and high-speed clone selection with Kemp Proteins' molecular engineering capabiliti...
Scientists created an AI tool that can help to reveal how genes function together inside human cells dependent on the cellular context, which could ultimately help to support the d...
RNA sequencing with NTVE enables repeated monitoring of gene expression in living cells, supporting time-course analysis of differentiation, perturbation responses, and cellular dy...
RNA sequencing now enables simultaneous detection of multiple RNA modifications alongside gene expression, providing deeper...
This Parse Biosciences and bit.bio alliance combines single-cell RNA sequencing and causal transcriptomics to map transcription factor-driven cell identity, enabling improved disea...
RNA sequencing captures both coding and noncoding RNAs at single-cell resolution, revealing complex regulatory programs and cellular identities across development and disease...
New screening technologies from Garage Brain Science aim to identify abnormal protein signals years before clinical symptoms develop. The post Detecting Disease at Its Molecular Or...
Under the terms of the partnership, Seer's Proteograph product suite will be used to profile the plasma proteome in samples from 10,000 participants from the PRECISE-SG100k initiat...
RNA sequencing supports space biology research by enabling transcriptome-wide analysis of gene expression changes associated with spaceflight and adaptation to space environments.....
RNA sequencing improves sarcoma diagnosis by detecting gene fusions and refining classifications, enabling more accurate treatment decisions and better patient...
RNA sequencing combined with perturbation data enables PSGRN to improve gene regulatory network inference, enhancing accuracy in identifying gene interactions across single-cell...
by Clelia Corridori, Merrit Romeike, Giorgio Nicoletti, Christa Buecker, Samir Suweis, Sandro Azaele, Graziano Martello Physiological and pathological processes are governed by ne...
Integrated miRNA workflows connect sequencing, dPCR validation, and pathway analysis to improve cancer biomarker discovery and biological interpretation from challenging samples li...
RNA sequencing combined with multiomic analysis uncovers new therapeutic targets in advanced cancers, enabling identification of antibody drug conjugate options when DNA testing al...
RNA sequencing combined with protein analysis enables detailed tracking of immune cell activity, revealing cytokine dynamics and improving understanding of cancer and immune respon...
Takara Bio’s Trekker FX spatial transcriptomics improves single-cell resolution and detects more cell interactions, enhancing analysis of tumor microenvironments in cancer samples....
RNA sequencing combined with RNA velocity enabled prediction of disease progression, treatment response, and clinical outcomes using whole-blood gene expression patterns...
RNA sequencing reveals how transposable elements drive alternative splicing and alter translation in glioblastoma, generating diverse RNA isoforms linked to cancer progression...
Integrating RNA sequencing with whole genome analysis, Caris ChromoSeq delivers...
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