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Posts tagged #Transcriptomic

Mechanism-Aware Prediction of Tissue-Specific Drug Activity via Multi-Modal Biological Graphs

Sally Turutov, Kira Radinsky

Action editor: Romain Lopez

https://openreview.net/forum?id=UDW8m9iQeC

#transcriptomic #pathway #pathways

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Accelerate #singlecell gene expression research with high-res 3' GEX #scRNA-seq. We deliver sensitive, scalable #transcriptomic profiling with expert support from sample prep to analysis.

#Genomics #NGS #Bioinformatics #LifeSciences #Biotechnology #PrecisionMedicine https://tinyurl.com/2mb557nm

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#Molecular mechanisms underlying the #inhibition of #Sparassis latifolia #mycelial growth by #cycloleucine: a comprehensive #transcriptomic and #m6A methylome analysis
doi.org/10.1080/2150...
@tandfresearch.bsky.social

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Heat hormesis engages specific regulators to induce thermotolerance in WT and glp-1(ts) mutant. This study reveals that heat hormesis promotes longevity in WT and induces thermotolerance in both WT and glp-1(ts) mutant animals. The authors' multiomic data lead to the identification of several key regulators of heat hormesis, all of which are evolutionarily highly conserved, and participate in different regulatory steps of gene expression. HSF-1 is the master transcription factor of heat shock response and its emergence from the analyses proves that the investigative strategy is effective. FOS-1 points to a potential role for the AP-1 pioneer transcription factor complex in encoding heat hormesis memory through chromatin remodeling. ELT-2 suggests an interaction between the germline and the intestine in stress adaptation. DPY-27 suggests a connection between the dosage compensation complex (DCC)-mediated chromosome architecture and heat stress management. HSF-1, ELT-2, and DPY-27 regulate heat hormesis differently in worms with or without germline. SNPC-4 implicates a role of piRNA-mediated post-transcriptional regulation in stress responses. MARS-1 implicates a role of methionine incorporation during protein synthesis in heat hormesis. Created in BioRender. Lee, S. (2026)

Heat hormesis engages specific regulators to induce thermotolerance in WT and glp-1(ts) mutant. This study reveals that heat hormesis promotes longevity in WT and induces thermotolerance in both WT and glp-1(ts) mutant animals. The authors' multiomic data lead to the identification of several key regulators of heat hormesis, all of which are evolutionarily highly conserved, and participate in different regulatory steps of gene expression. HSF-1 is the master transcription factor of heat shock response and its emergence from the analyses proves that the investigative strategy is effective. FOS-1 points to a potential role for the AP-1 pioneer transcription factor complex in encoding heat hormesis memory through chromatin remodeling. ELT-2 suggests an interaction between the germline and the intestine in stress adaptation. DPY-27 suggests a connection between the dosage compensation complex (DCC)-mediated chromosome architecture and heat stress management. HSF-1, ELT-2, and DPY-27 regulate heat hormesis differently in worms with or without germline. SNPC-4 implicates a role of piRNA-mediated post-transcriptional regulation in stress responses. MARS-1 implicates a role of methionine incorporation during protein synthesis in heat hormesis. Created in BioRender. Lee, S. (2026)

Exposure to mild #HeatStress can promote stress resilience & healthy aging ("heat hormesis"). siusylvialee.bsky.social &co characterize #transcriptomic & #chromatin accessibility changes during heat #hormesis in #Celegans, identifying several novel regulators @plosbiology.org 🧪 plos.io/4cJFEa9

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Transcriptomic response analysis of rubber tree saplings to water-deficit stress at single-cell resolution - Communications Biology Single-cell profiling in rubber tree saplings to water-deficit stress identifies seven bark cell types and ABA-mediated drought responses, including uniform ABF2/3/4 induction.

#Transcriptomic response analysis of rubber #tree saplings to #water-deficit stress at #single-cell resolution

www.nature.com/articles/s42...

#PlantScience @commsbio.nature.com @cyi12.bsky.social @treemortality.bsky.social @singlecell.broadinstitute.org @unccd.bsky.social @wtscotsocial.bsky.social

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Heat hormesis engages specific regulators to induce thermotolerance in WT and glp-1(ts) mutant. This study reveals that heat hormesis promotes longevity in WT and induces thermotolerance in both WT and glp-1(ts) mutant animals. The authors' multiomic data lead to the identification of several key regulators of heat hormesis, all of which are evolutionarily highly conserved, and participate in different regulatory steps of gene expression. HSF-1 is the master transcription factor of heat shock response and its emergence from the analyses proves that the investigative strategy is effective. FOS-1 points to a potential role for the AP-1 pioneer transcription factor complex in encoding heat hormesis memory through chromatin remodeling. ELT-2 suggests an interaction between the germline and the intestine in stress adaptation. DPY-27 suggests a connection between the dosage compensation complex (DCC)-mediated chromosome architecture and heat stress management. HSF-1, ELT-2, and DPY-27 regulate heat hormesis differently in worms with or without germline. SNPC-4 implicates a role of piRNA-mediated post-transcriptional regulation in stress responses. MARS-1 implicates a role of methionine incorporation during protein synthesis in heat hormesis. Created in BioRender. Lee, S. (2026)

Heat hormesis engages specific regulators to induce thermotolerance in WT and glp-1(ts) mutant. This study reveals that heat hormesis promotes longevity in WT and induces thermotolerance in both WT and glp-1(ts) mutant animals. The authors' multiomic data lead to the identification of several key regulators of heat hormesis, all of which are evolutionarily highly conserved, and participate in different regulatory steps of gene expression. HSF-1 is the master transcription factor of heat shock response and its emergence from the analyses proves that the investigative strategy is effective. FOS-1 points to a potential role for the AP-1 pioneer transcription factor complex in encoding heat hormesis memory through chromatin remodeling. ELT-2 suggests an interaction between the germline and the intestine in stress adaptation. DPY-27 suggests a connection between the dosage compensation complex (DCC)-mediated chromosome architecture and heat stress management. HSF-1, ELT-2, and DPY-27 regulate heat hormesis differently in worms with or without germline. SNPC-4 implicates a role of piRNA-mediated post-transcriptional regulation in stress responses. MARS-1 implicates a role of methionine incorporation during protein synthesis in heat hormesis. Created in BioRender. Lee, S. (2026)

Exposure to mild #HeatStress can promote stress resilience & healthy aging ("heat hormesis"). siusylvialee.bsky.social &co characterize #transcriptomic & #chromatin accessibility changes during heat #hormesis in #Celegans, identifying several novel regulators @plosbiology.org 🧪 plos.io/4cJFEa9

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Heat hormesis engages specific regulators to induce thermotolerance in WT and glp-1(ts) mutant. This study reveals that heat hormesis promotes longevity in WT and induces thermotolerance in both WT and glp-1(ts) mutant animals. The authors' multiomic data lead to the identification of several key regulators of heat hormesis, all of which are evolutionarily highly conserved, and participate in different regulatory steps of gene expression. HSF-1 is the master transcription factor of heat shock response and its emergence from the analyses proves that the investigative strategy is effective. FOS-1 points to a potential role for the AP-1 pioneer transcription factor complex in encoding heat hormesis memory through chromatin remodeling. ELT-2 suggests an interaction between the germline and the intestine in stress adaptation. DPY-27 suggests a connection between the dosage compensation complex (DCC)-mediated chromosome architecture and heat stress management. HSF-1, ELT-2, and DPY-27 regulate heat hormesis differently in worms with or without germline. SNPC-4 implicates a role of piRNA-mediated post-transcriptional regulation in stress responses. MARS-1 implicates a role of methionine incorporation during protein synthesis in heat hormesis. Created in BioRender. Lee, S. (2026)

Heat hormesis engages specific regulators to induce thermotolerance in WT and glp-1(ts) mutant. This study reveals that heat hormesis promotes longevity in WT and induces thermotolerance in both WT and glp-1(ts) mutant animals. The authors' multiomic data lead to the identification of several key regulators of heat hormesis, all of which are evolutionarily highly conserved, and participate in different regulatory steps of gene expression. HSF-1 is the master transcription factor of heat shock response and its emergence from the analyses proves that the investigative strategy is effective. FOS-1 points to a potential role for the AP-1 pioneer transcription factor complex in encoding heat hormesis memory through chromatin remodeling. ELT-2 suggests an interaction between the germline and the intestine in stress adaptation. DPY-27 suggests a connection between the dosage compensation complex (DCC)-mediated chromosome architecture and heat stress management. HSF-1, ELT-2, and DPY-27 regulate heat hormesis differently in worms with or without germline. SNPC-4 implicates a role of piRNA-mediated post-transcriptional regulation in stress responses. MARS-1 implicates a role of methionine incorporation during protein synthesis in heat hormesis. Created in BioRender. Lee, S. (2026)

Exposure to mild #HeatStress can promote stress resilience & healthy aging ("heat hormesis"). siusylvialee.bsky.social &co characterize #transcriptomic & #chromatin accessibility changes during heat #hormesis in #Celegans, identifying several novel regulators @plosbiology.org 🧪 plos.io/4cJFEa9

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Diet induces sex-divergent motif enrichment in liver. Top: Correlation analysis of ATAC-seq peaks in male and female mice fed a WD. Dashed lines indicate 1.2-fold change. Middle left: Strategy for analysis of motifs by group. Roman numerals represent the peak groups selected for motif analysis, which were subsequently used in Fig 3D and 3E. Bottom right: Heatmap showing the relative level of peaks selected from Fig 3B, separated by group. Top single motif from each group enriched in the motifs analysis (motif families identified with HOMER).

Diet induces sex-divergent motif enrichment in liver. Top: Correlation analysis of ATAC-seq peaks in male and female mice fed a WD. Dashed lines indicate 1.2-fold change. Middle left: Strategy for analysis of motifs by group. Roman numerals represent the peak groups selected for motif analysis, which were subsequently used in Fig 3D and 3E. Bottom right: Heatmap showing the relative level of peaks selected from Fig 3B, separated by group. Top single motif from each group enriched in the motifs analysis (motif families identified with HOMER).

Metabolic diseases are often influenced by #BiologicalSex. This study shows how sex and diet interact to shape molecular responses in the mouse #liver, revealing how gonadal & chromosomal sex influence diet-induced #transcriptomic & #chromatin dynamics @plosbiology.org 🧪 plos.io/4aP440z

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Diet induces sex-divergent motif enrichment in liver. Top: Correlation analysis of ATAC-seq peaks in male and female mice fed a WD. Dashed lines indicate 1.2-fold change. Middle left: Strategy for analysis of motifs by group. Roman numerals represent the peak groups selected for motif analysis, which were subsequently used in Fig 3D and 3E. Bottom right: Heatmap showing the relative level of peaks selected from Fig 3B, separated by group. Top single motif from each group enriched in the motifs analysis (motif families identified with HOMER).

Diet induces sex-divergent motif enrichment in liver. Top: Correlation analysis of ATAC-seq peaks in male and female mice fed a WD. Dashed lines indicate 1.2-fold change. Middle left: Strategy for analysis of motifs by group. Roman numerals represent the peak groups selected for motif analysis, which were subsequently used in Fig 3D and 3E. Bottom right: Heatmap showing the relative level of peaks selected from Fig 3B, separated by group. Top single motif from each group enriched in the motifs analysis (motif families identified with HOMER).

Metabolic diseases are often influenced by #BiologicalSex. This study shows how sex and diet interact to shape molecular responses in the mouse #liver, revealing how gonadal & chromosomal sex influence diet-induced #transcriptomic & #chromatin dynamics @plosbiology.org 🧪 plos.io/4aP440z

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Diet induces sex-divergent motif enrichment in liver. Top: Correlation analysis of ATAC-seq peaks in male and female mice fed a WD. Dashed lines indicate 1.2-fold change. Middle left: Strategy for analysis of motifs by group. Roman numerals represent the peak groups selected for motif analysis, which were subsequently used in Fig 3D and 3E. Bottom right: Heatmap showing the relative level of peaks selected from Fig 3B, separated by group. Top single motif from each group enriched in the motifs analysis (motif families identified with HOMER).

Diet induces sex-divergent motif enrichment in liver. Top: Correlation analysis of ATAC-seq peaks in male and female mice fed a WD. Dashed lines indicate 1.2-fold change. Middle left: Strategy for analysis of motifs by group. Roman numerals represent the peak groups selected for motif analysis, which were subsequently used in Fig 3D and 3E. Bottom right: Heatmap showing the relative level of peaks selected from Fig 3B, separated by group. Top single motif from each group enriched in the motifs analysis (motif families identified with HOMER).

Metabolic diseases are often influenced by #BiologicalSex. This study shows how sex and diet interact to shape molecular responses in the mouse #liver, revealing how gonadal & chromosomal sex influence diet-induced #transcriptomic & #chromatin dynamics @plosbiology.org 🧪 plos.io/4aP440z

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By systematically curating published #transcriptomic datasets of aging mouse #macrophages, Ella tried to answer the question of whether #macrophage aging follows a common blueprint or shows sex- and niche-specific patterns. Intringuingly, niche was the strongest effect on aging trajectories. 2/4

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GeARF5/GeIAA33‐GeSWEET14 module balances the secondary metabolic biosynthesis to increase the yield and quality in Gastrodia elata Auxin signaling regulates the formation of vegetative propagation corms in Gastrodia elata by regulating sugar-acid interconversion, which in turn regulates polysaccharide and starch biosynthesis as ....

[📰 Paper] GeARF5/GeIAA33-GeSWEET14 module balances the secondary metabolic biosynthesis to increase the yield and quality in 𝐺𝑎𝑠𝑡𝑟𝑜𝑑𝑖𝑎 𝑒𝑙𝑎𝑡𝑎

@cnrs-rhoneauvergne.bsky.social @vocspop.bsky.social

#paper #medicinalplant #science #biosynthesis #gastrodia #transcriptomic

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#Transcriptomic #meta-analysis of #immunecells in #chronicpain conditions identified genes and sex-specific signatures in this new study from Perez & Tawflig

www.bjanaesthesia.org/article/S0007-0912(25)00...

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@chijing-leow.bsky.social
Life History-Dependent Brain #Transcriptomic Signatures in Nothobranchids: Insights into Aging, #Neurogenesis, and Life History #Evolution

in IOB (SICB’s OA journal)
Leow , et al , doi.org/10.1093/iob/...

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Using #brain #genomic and #transcriptomic data from UK Biobank, Maya Sharma and Heather Wheeler identified genetic variation underlying #anxiety in diverse ancestral populations.

Learn more in #G3journal: buff.ly/MWQtn7Y

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HSCT-64, a 64-gene #Transcriptomic #RiskModel enables #Diagnosis-time identification of pediatric #AML patients most likely to benefit from #Transplantation, providing a practical approach for #PersonalizedTreatment.

#OpenAccess: doi.org/10.1016/j.ge...

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Curious about spatial omics and hands-on multi-omics analysis? 🧬
Explore spatial platforms, learn SPArrOW/Harpy & Cardinal, and discover multi-omics integration strategies at our summer school.
⏰ Deadline to register: 2nd February
#SpatialOmics #SpatialBiology #MultiOmics #Transcriptomic #Proteomics

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Spatiotemporal molecular and cellular atlas of mouse PFC during postnatal development. Top left: UMAP of all cells in mouse PFC from scRNA-seq data, colored by cell subtypes. Im, immature. Top right: UMAP of all cells in mouse PFC from scRNA-seq data, colored by time stages. Bottom left: Spatial distribution of all cell subtypes in mouse PFC from P1 stereo-seq data. Bottom right: Spatial distribution of all cell subtypes in mouse PFC from adult stereo-seq data.

Spatiotemporal molecular and cellular atlas of mouse PFC during postnatal development. Top left: UMAP of all cells in mouse PFC from scRNA-seq data, colored by cell subtypes. Im, immature. Top right: UMAP of all cells in mouse PFC from scRNA-seq data, colored by time stages. Bottom left: Spatial distribution of all cell subtypes in mouse PFC from P1 stereo-seq data. Bottom right: Spatial distribution of all cell subtypes in mouse PFC from adult stereo-seq data.

The #PrefrontalCortex is key for higher cognitive functions, but how do its circuits mature? This study provides a #transcriptomic resource for the mouse #PFC over 84 days of development, revealing cell population dynamics & expression of #psychiatric risk genes
@plosbiology.org 🧪 plos.io/45bhRLU

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Spatiotemporal molecular and cellular atlas of mouse PFC during postnatal development. Top left: UMAP of all cells in mouse PFC from scRNA-seq data, colored by cell subtypes. Im, immature. Top right: UMAP of all cells in mouse PFC from scRNA-seq data, colored by time stages. Bottom left: Spatial distribution of all cell subtypes in mouse PFC from P1 stereo-seq data. Bottom right: Spatial distribution of all cell subtypes in mouse PFC from adult stereo-seq data.

Spatiotemporal molecular and cellular atlas of mouse PFC during postnatal development. Top left: UMAP of all cells in mouse PFC from scRNA-seq data, colored by cell subtypes. Im, immature. Top right: UMAP of all cells in mouse PFC from scRNA-seq data, colored by time stages. Bottom left: Spatial distribution of all cell subtypes in mouse PFC from P1 stereo-seq data. Bottom right: Spatial distribution of all cell subtypes in mouse PFC from adult stereo-seq data.

The #PrefrontalCortex is key for higher cognitive functions, but how do its circuits mature? This study provides a #transcriptomic resource for the mouse #PFC over 84 days of development, revealing cell population dynamics & expression of #psychiatric risk genes
@plosbiology.org 🧪 plos.io/45bhRLU

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Spatiotemporal molecular and cellular atlas of mouse PFC during postnatal development. Top left: UMAP of all cells in mouse PFC from scRNA-seq data, colored by cell subtypes. Im, immature. Top right: UMAP of all cells in mouse PFC from scRNA-seq data, colored by time stages. Bottom left: Spatial distribution of all cell subtypes in mouse PFC from P1 stereo-seq data. Bottom right: Spatial distribution of all cell subtypes in mouse PFC from adult stereo-seq data.

Spatiotemporal molecular and cellular atlas of mouse PFC during postnatal development. Top left: UMAP of all cells in mouse PFC from scRNA-seq data, colored by cell subtypes. Im, immature. Top right: UMAP of all cells in mouse PFC from scRNA-seq data, colored by time stages. Bottom left: Spatial distribution of all cell subtypes in mouse PFC from P1 stereo-seq data. Bottom right: Spatial distribution of all cell subtypes in mouse PFC from adult stereo-seq data.

The #PrefrontalCortex is key for higher cognitive functions, but how do its circuits mature? This study provides a #transcriptomic resource for the mouse #PFC over 84 days of development, revealing cell population dynamics & expression of #psychiatric risk genes @plosbiology.org 🧪 plos.io/45bhRLU

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Latest in #G3journal: #Transcriptomic analysis to understand transcriptional responses to dehydration in drought-tolerant oak from a local population in the Sierra Nevada Foothills in California identifies potential genes with relevance in #drought stress. buff.ly/sRuwnbl

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The latest issue of #G3journal features a curated database of stress-responsive genes in maize across stressors from @annapardo-phd.bsky.social, @bobvanburen.bsky.social, and colleagues generated via meta-analysis of public #transcriptomic data.

Learn more about this resource here: buff.ly/znaNWQg

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Following our Dec 5 article on #MMVD molecular profiling, Romain Capoulade’s editorial offers valuable perspective on the #transcriptomic, #miRNA, and machine-learning findings—and what they may mean for future therapies.

🗨️ Which insight do you find most impactful?
➡️ Read more: shorturl.at/UArNa

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Single-cell spatiotemporal transcriptomic and chromatin accessibility profiling in developing postnatal human and macaque prefrontal cortex - Nature Neuroscience Human-specific molecular and cellular regulatory programs prolong prefrontal cortical maturation by orchestrating postnatal development of neurons and glia, with implications for cognitive function an...

Single-cell spatiotemporal #transcriptomic and #chromatin accessibility profiling in #developing postnatal #human and #macaque prefrontal #cortex
doi.org/10.1038/s415...

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Response regression model as a guiding principle for pharmacological mechanistic investigation of host-targeted antivirals Using a response regression model as a guiding principle to precisely explore the pharmacological mechanisms of host-targeted antiviral (HTA) agents.

This study presents a response regression model for analyzing #Transcriptomic data on #ViralInfection, which serves as a guiding principle to identify specific target host factors influenced by the #Pharmacological effects of host-targeted #Antivirals.

#OpenAccess: amm-journal.org/index.php/20...

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Spatiotemporal transcriptomic insights into ferroptosis and TFRC-linked immune interactions in ischemia-reperfusion acute kidney injury - Genes & Immunity Genes & Immunity - Spatiotemporal transcriptomic insights into ferroptosis and TFRC-linked immune interactions in ischemia-reperfusion acute kidney injury

💥 #Cool #Research #Alert

#Spatiotemporal #transcriptomic insights into #ferroptosis and TFRC-linked #immune #interactions in #ischemia-#reperfusion acute #kidney #injury

#Genes & #Immunity @springernature.com
www.nature.com/articles/s41...

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Polymorphism in a metabolic gene involved in sexual selection shapes global gene expression profiles in the bulb mite males Abstract. Uncovering the genetic basis of sexually selected traits and traits involved in sexual conflict is a key to understand the association between se

A #transcriptomic study shows that single nucleotide polymorphisms in #6Pgdh - a metabolic gene involved in #sexualselection and conflict in bulb mite, Rhizoglyphus robini - can be associated with genome wide gene expression differences:

doi.org/10.1093/jeb/...

Plesnar-Bielak et al. 2025

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CellNavi predicts genes directing cellular transitions by learning a gene graph-enhanced cell state manifold - Nature Cell Biology The authors integrate single-cell transcriptomic data with prior gene graphs to produce a biologically meaningful cell state manifold that can predict driver genes for genetic perturbations and differ...

☕The authors integrate single-cell #transcriptomic data with prior gene graphs to produce a biologically meaningful cell state manifold that can predict driver genes for #genetic perturbations and differentiation events across diverse cell types.
bit.ly/4nIarpI

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Comparative #transcriptomic analysis of #Chinese #cabbage’s defense responses to #Alternaria brassicae
🥬https://doi.org/10.1016/j.jia.2025.06.024
✏️Prof. Baohua Li team from Northwest A&F University
🔗Chinese tweet shorturl.at/cxQiC
#horticulture #plantsci

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Integrated #transcriptomic and metabolomic analyses reveal a novel mechanism of resistance to #Colletotrichum fructicola in #pear
🍐https://doi.org/10.1016/j.jia.2024.12.041
#horticulture #plantsci

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