All Stories

  1. Multimodal learning enables chat-based exploration of single-cell data
  2. Systematic discovery of CRISPR-boosted CAR T cell immunotherapies
  3. Quantitative profiling of human brain organoid cell diversity across four protocols and multiple cell lines
  4. Single‐cell multi‐omics characterize colorectal tumors, adjacent healthy tissue and matched (tumor) organoids identifying CRC ‐unique features
  5. Unveiling genetic signatures of immune response in immune-related diseases through single-cell eQTL analysis across diverse conditions
  6. Molecularly informed analysis of histopathology images using natural language
  7. HDAC1 controls the generation and maintenance of effector-like CD8+ T cells during chronic viral infection
  8. Protecting centrosomes from fracturing enables efficient cell navigation
  9. PHLPP2 is a pseudophosphatase that lost activity in the metazoan ancestor
  10. Single-cell and chromatin accessibility profiling reveals regulatory programs of pathogenic Th2 cells in allergic asthma
  11. 24-Nor-ursodeoxycholic acid improves intestinal inflammation by targeting T H 17 pathogenicity and transdifferentiation
  12. Cell-type-specific requirement for TYK2 in murine immune cells under steady state and challenged conditions
  13. Altered spawning seasons of Atlantic salmon broodstock transcriptionally and epigenetically influence cell cycle and lipid-mediated regulations in their offspring
  14. Single-cell CRISPR screening in mouse brain
  15. Time-resolved immune dynamics in rheumatoid arthritis under methotrexate therapy
  16. Reconstitution of Human Brain Cell Diversity in Organoids via Four Protocols
  17. Engineering Next-Generation CAR T Cells Via Genetic Screens
  18. Nuclear receptor corepressor 1 controls regulatory T cell subset differentiation and effector function
  19. Multimodal learning of transcriptomes and text enables interactive single-cell RNA-seq data exploration with natural-language chats
  20. Mechanical Centrosome Fracturing during Cell Navigation
  21. Targeting T cell plasticity in kidney and gut inflammation by pooled single-cell CRISPR screening
  22. Mapping the brain’s gene-regulatory maze
  23. Aberrant Lipid Metabolism in Macrophages Is Associated with Granuloma Formation in Sarcoidosis
  24. Adaptive immune responses are larger and functionally preserved in a hypervaccinated individual
  25. Baseline JAK–STAT signaling maintains immune cell homeostasis
  26. JAK-STAT signaling maintains homeostasis in T cells and macrophages
  27. Hyperactive STAT5 hijacks T cell receptor signaling and drives immature T cell acute lymphoblastic leukemia
  28. Transient expression of the neuropeptide galanin modulates peripheral‑to‑central connectivity in the somatosensory thalamus during whisker development in mice
  29. HDAC1 controls the generation and maintenance of effector-like CD8 + T cells during chronic viral infection
  30. One-carbon metabolism nutrients impact the interplay between DNA methylation and gene expression in liver, enhancing protein synthesis in Atlantic salmon
  31. Altered spawning seasons of Atlantic salmon broodstock transcriptionally and epigenetically influence cell cycle and lipid-mediated regulations in their offspring
  32. Multi‐organ single‐cell RNA sequencing in mice reveals early hyperglycemia responses that converge on fibroblast dysregulation
  33. Efficacy and safety of mTOR inhibition in cutaneous sarcoidosis: a single-centre trial
  34. The pathophysiology of sepsis and precision-medicine-based immunotherapy
  35. Multi-omics analysis of innate and adaptive responses to BCG vaccination reveals epigenetic cell states that predict trained immunity
  36. Multipotent progenitors instruct ontogeny of the superior colliculus
  37. Endoscope-enhanced fluorescence-guided microsurgery increases survival in patients with glioblastoma
  38. Metabolic support by macrophages sustains colonic epithelial homeostasis
  39. One-carbon metabolism nutrients impact the interplay between DNA methylation and gene expression in liver, enhancing protein synthesis in Atlantic Salmon
  40. Biallelic NFATC1 mutations cause an inborn error of immunity with impaired CD8+ T-cell function and perturbed glycolysis
  41. Pharmacological perturbation of the phase-separating protein SMNDC1
  42. Cell-autonomous regulation of complement C3 by factor H limits macrophage efferocytosis and exacerbates atherosclerosis
  43. Large language models are universal biomedical simulators
  44. Buffy coat signatures of breast cancer risk in a prospective cohort study
  45. Multipotent Progenitors Instruct Ontogeny of the Superior Colliculus
  46. Epigenetic regulation of T cell lineages in skin and blood following hematopoietic stem cell transplantation
  47. Comparative analysis of genome-scale, base-resolution DNA methylation profiles across 580 animal species
  48. Radiomic features define risk and are linked to DNA methylation attributes in primary CNS lymphoma
  49. Interleukin‐6 initiates muscle‐ and adipose tissue wasting in a novel C57BL/6 model of cancer‐associated cachexia
  50. Early anteroposterior regionalisation of human neural crest is shaped by a pro-mesodermal factor
  51. SMNDC1 links chromatin remodeling and splicing to regulate pancreatic hormone expression
  52. Nuclear receptor corepressor 1 controls regulatory T cell subset differentiation and effector function
  53. High-content CRISPR screening
  54. Rapid neutrophil mobilization by VCAM-1+ endothelial cell-derived extracellular vesicles
  55. LIQUORICE: detection of epigenetic signatures in liquid biopsies based on whole-genome sequencing data
  56. Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation
  57. Comprehensive approach for identification of functional FCGR2C alleles resulting in protein expression as a determinant for predicting predisposition to autoimmunity
  58. Rapid, early and accurate SARS-CoV-2 detection using RT-qPCR in primary care: a prospective cohort study (REAP-1)
  59. Single-cell analysis reveals innate lymphoid cell lineage infidelity in atopic dermatitis
  60. High-throughput Mutational Surveillance of the SARS-CoV-2 Spike Gene
  61. High-throughput drug screening identifies the ATR-CHK1 pathway as a therapeutic vulnerability of CALR mutated hematopoietic cells
  62. Genomic imprinting in mouse blastocysts is predominantly associated with H3K27me3
  63. Ultra-high-throughput single-cell RNA sequencing and perturbation screening with combinatorial fluidic indexing
  64. Multimodal analysis of cell-free DNA whole-genome sequencing for pediatric cancers with low mutational burden
  65. Hematopoietic expression of a chimeric murine‐human CALR oncoprotein allows the assessment of anti‐CALR antibody immunotherapies in vivo
  66. Histone deacetylase 1 controls CD4+ T cell trafficking in autoinflammatory diseases
  67. Complex Interplay Between MAZR and Runx3 Regulates the Generation of Cytotoxic T Lymphocyte and Memory T Cells
  68. SARS-CoV-2 mutations in MHC-I–restricted epitopes evade CD8 + T cell responses
  69. Temporal dissection of an enhancer cluster reveals distinct temporal and functional contributions of individual elements
  70. Spontaneously Resolved Atopic Dermatitis Shows Melanocyte and Immune Cell Activation Distinct From Healthy Control Skin
  71. Precision Medicine in Hematology 2021: Definitions, Tools, Perspectives, and Open Questions
  72. αβγδ T cells play a vital role in fetal human skin development and immunity
  73. Acute BAF perturbation causes immediate changes in chromatin accessibility
  74. Publisher Correction: Rational discovery of molecular glue degraders via scalable chemical profiling
  75. Persistence of mature dendritic cells, T H 2A, and Tc2 cells characterize clinically resolved atopic dermatitis under IL-4Rα blockade
  76. The Organoid Cell Atlas
  77. RANK links thymic regulatory T cells to fetal loss and gestational diabetes in pregnancy
  78. STAT3 promotes melanoma metastasis by CEBP-induced repression of the MITF pathway
  79. Requirement of DNMT1 to orchestrate epigenomic reprogramming for NPM-ALK–driven lymphomagenesis
  80. Genomic epidemiology of superspreading events in Austria reveals mutational dynamics and transmission properties of SARS-CoV-2
  81. Long-term skin-resident memory T cells proliferate in situ and are involved in human graft-versus-host disease
  82. Single-Cell RNA Sequencing Analysis Reveals a Crucial Role for CTHRC1 (Collagen Triple Helix Repeat Containing 1) Cardiac Fibroblasts After Myocardial Infarction
  83. Anti-Apoptotic Molecule BCL2 Is a Therapeutic Target in Steroid-Refractory Graft-Versus-Host Disease
  84. Single-cell transcriptomics combined with interstitial fluid proteomics defines cell type–specific immune regulation in atopic dermatitis
  85. Distributed changes of the functional connectome in patients with glioblastoma
  86. A discrete subset of epigenetically primed human NK cells mediates antigen-specific immune responses
  87. Disturbed mitochondrial dynamics in CD8+ TILs reinforce T cell exhaustion
  88. Circadian rhythm influences induction of trained immunity by BCG vaccination
  89. LifeTime and improving European healthcare through cell-based interceptive medicine
  90. Emergence of coronavirus disease 2019 (COVID-19) in Austria
  91. Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020
  92. Knowledge-primed neural networks enable biologically interpretable deep learning on single-cell sequencing data
  93. Rational discovery of molecular glue degraders via scalable chemical profiling
  94. The cytoskeletal regulator HEM1 governs B cell development and prevents autoimmunity
  95. Cell-Type Specificity of Genomic Imprinting in Cerebral Cortex
  96. Structural cells are key regulators of organ-specific immune responses
  97. Selective Mediator dependence of cell-type-specifying transcription
  98. Detailed temporal dissection of an enhancer cluster reveals two distinct roles for individual elements
  99. Molecular design of hypothalamus development
  100. Single-cell RNA-seq with spike-in cells enables accurate quantification of cell-specific drug effects in pancreatic islets
  101. NCOR1 Orchestrates Transcriptional Landscapes and Effector Functions of CD4+ T Cells
  102. Microbiota-Derived Metabolites Suppress Arthritis by Amplifying Aryl-Hydrocarbon Receptor Activation in Regulatory B Cells
  103. Targeting clinical epigenetic reprogramming for chemoprevention of metabolic and viral hepatocellular carcinoma
  104. DNA methylation QTL analysis identifies new regulators of human longevity
  105. Quantitative comparison of within-sample heterogeneity scores for DNA methylation data
  106. Histone deacetylases 1 and 2 restrain CD4+ cytotoxic T lymphocyte differentiation
  107. Precursors for Nonlymphoid-Tissue Treg Cells Reside in Secondary Lymphoid Organs and Are Programmed by the Transcription Factor BATF
  108. Chromatin mapping and single-cell immune profiling define the temporal dynamics of ibrutinib response in CLL
  109. Ultra-high throughput single-cell RNA sequencing by combinatorial fluidic indexing
  110. The Transcription Factor MAZR/PATZ1 Regulates the Development of FOXP3+ Regulatory T Cells
  111. Life‐long impairment of glucose homeostasis upon prenatal exposure to psychostimulants
  112. Longitudinal molecular trajectories of diffuse glioma in adults
  113. Life-long epigenetic programming of cortical architecture by maternal ‘Western’ diet during pregnancy
  114. Aryl Hydrocarbon Receptor Contributes to the Transcriptional Program of IL-10-Producing Regulatory B Cells
  115. Genome-scale CRISPR screens are efficient in non-homologous end-joining deficient cells
  116. Inference of transcription factor binding from cell-free DNA enables tumor subtype prediction and early detection
  117. Guadecitabine plus ipilimumab in unresectable melanoma: the NIBIT-M4 clinical trial
  118. B cells sustain inflammation and predict response to immune checkpoint blockade in human melanoma
  119. Systematic characterization of BAF mutations provides insights into intracomplex synthetic lethalities in human cancers
  120. Epigenomics and Single-Cell Sequencing Define a Developmental Hierarchy in Langerhans Cell Histiocytosis
  121. Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms
  122. Mitochondria Are a Subset of Extracellular Vesicles Released by Activated Monocytes and Induce Type I IFN and TNF Responses in Endothelial Cells
  123. Spatiotemporal structure of cell fate decisions in murine neural crest
  124. HCV-Induced Epigenetic Changes Associated With Liver Cancer Risk Persist After Sustained Virologic Response
  125. MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation
  126. CDK6 coordinates JAK2V617F mutant MPN via NF-κB and apoptotic networks
  127. RnBeads 2.0: comprehensive analysis of DNA methylation data
  128. NK Cells Require Cell-Extrinsic and -Intrinsic TYK2 for Full Functionality in Tumor Surveillance and Antibacterial Immunity
  129. Combined chemosensitivity and chromatin profiling prioritizes drug combinations in CLL
  130. Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes
  131. Integrative Proteomic Profiling Reveals PRC2-Dependent Epigenetic Crosstalk Maintains Ground-State Pluripotency
  132. The ERBB-STAT3 Axis Drives Tasmanian Devil Facial Tumor Disease
  133. Colocalization analyses of genomic elements: approaches, recommendations and challenges
  134. The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space
  135. Functional Dissection of the Enhancer Repertoire in Human Embryonic Stem Cells
  136. Epigenome-based prediction of gene expression across species
  137. Coloc-stats: a unified web interface to perform colocalization analysis of genomic features
  138. An ERK-Dependent Feedback Mechanism Prevents Hematopoietic Stem Cell Exhaustion
  139. Targeted mutation screening of 292 candidate genes in 38 children with inborn haematological cytopenias efficiently identifies novel disease-causing mutations
  140. Assessment of established techniques to determine developmental and malignant potential of human pluripotent stem cells
  141. The ERBB-STAT3 Axis Drives Tasmanian Devil Facial Tumor Disease
  142. MIRA: an R package for DNA methylation-based inference of regulatory activity
  143. Ageing-associated DNA methylation dynamics are a molecular readout of lifespan variation among mammalian species
  144. Parental micronutrient deficiency distorts liver DNA methylation and expression of lipid genes associated with a fatty-liver-like phenotype in offspring
  145. Glioma through the looking GLASS: molecular evolution of diffuse gliomas and the Glioma Longitudinal Analysis Consortium
  146. STAT5BN642H is a driver mutation for T cell neoplasia
  147. Proposed Terminology and Classification of Pre-Malignant Neoplastic Conditions: A Consensus Proposal
  148. Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
  149. A T cell-specific deletion of HDAC1 protects against experimental autoimmune encephalomyelitis
  150. Mapping the mouse Allelome reveals tissue-specific regulation of allelic expression
  151. Functional dissection of the enhancer repertoire in human embryonic stem cells
  152. A combinatorial screen of the CLOUD uncovers a synergy targeting the androgen receptor
  153. VCF.Filter: interactive prioritization of disease-linked genetic variants from sequencing data
  154. DeepBlueR: large-scale epigenomic analysis in R
  155. Malondialdehyde epitopes are sterile mediators of hepatic inflammation in hypercholesterolemic mice
  156. DNA methylation heterogeneity defines a disease spectrum in Ewing sarcoma
  157. Pooled CRISPR screening with single-cell transcriptome readout
  158. Artemisinins Target GABAA Receptor Signaling and Impair α Cell Identity
  159. Molecular interrogation of hypothalamic organization reveals distinct dopamine neuronal subtypes
  160. Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia
  161. DNA Methylation Dynamics of Human Hematopoietic Stem Cell Differentiation
  162. The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
  163. Epigenetic Homogeneity Within Colorectal Tumors Predicts Shorter Relapse-Free and Overall Survival Times for Patients With Locoregional Cancer
  164. Preserve personal freedom in networked societies
  165. Specification of tissue-resident macrophages during organogenesis
  166. Multi-Omics of Single Cells: Strategies and Applications
  167. Parallel reverse genetic screening in mutant human cells using transcriptomics
  168. Quantitative comparison of DNA methylation assays for biomarker development and clinical applications
  169. Chromatin accessibility maps of chronic lymphocytic leukaemia identify subtype-specific epigenome signatures and transcription regulatory networks
  170. Making sense of big data in health research: Towards an EU action plan
  171. Familial early-onset dementia with complex neuropathologic phenotype and genomic background
  172. Next-generation sequencing identifies major DNA methylation changes during progression of Ph+ chronic myeloid leukemia
  173. Mapping the chemical chromatin reactivation landscape identifies BRD4-TAF1 cross-talk
  174. Comprehensive genome and epigenome characterization of CHO cells in response to evolutionary pressures and over time
  175. DeepBlue epigenomic data server: programmatic data retrieval and analysis of epigenome region sets
  176. A Comprehensive Analysis of the Dynamic Response to Aphidicolin-Mediated Replication Stress Uncovers Targets for ATM and ATMIN
  177. Single‐cell transcriptomes reveal characteristic features of human pancreatic islet cell types
  178. Differential DNA Methylation Analysis without a Reference Genome
  179. LOLA: enrichment analysis for genomic region sets and regulatory elements in R and Bioconductor
  180. Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms
  181. ChIPmentation: fast, robust, low-input ChIP-seq for histones and transcription factors
  182. Toward understanding and exploiting tumor heterogeneity
  183. Pharmacological targeting of the Wdr5-MLL interaction in C/EBPα N-terminal leukemia
  184. Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections
  185. Imprinted expression in cystic embryoid bodies shows an embryonic and not an extra-embryonic pattern
  186. Dissecting the role of aberrant DNA methylation in human leukaemia
  187. KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia
  188. Improving reference epigenome catalogs by computational prediction
  189. Notch-mediated expansion of cord blood progenitors: maintenance of transcriptional and epigenetic fidelity
  190. Single-Cell DNA Methylome Sequencing and Bioinformatic Inference of Epigenomic Cell-State Dynamics
  191. Epigenome Mapping Reveals Distinct Modes of Gene Regulation and Widespread Enhancer Reprogramming by the Oncogenic Fusion Protein EWS-FLI1
  192. Model-Based Whole-Genome Analysis of DNA Methylation Fidelity
  193. DNA methylation signatures link prenatal famine exposure to growth and metabolism
  194. NOTCH1 activation in breast cancer confers sensitivity to inhibition of SUMOylation
  195. Comprehensive analysis of DNA methylation data with RnBeads
  196. Regulation of DNA Methylation Patterns by CK2-Mediated Phosphorylation of Dnmt3a
  197. Notch inhibition allows oncogene-independent generation of iPS cells
  198. BiQ Analyzer HiMod: an interactive software tool for high-throughput locus-specific analysis of 5-methylcytosine and its oxidized derivatives
  199. Epigenomic Profiling of Young and Aged HSCs Reveals Concerted Changes during Aging that Reinforce Self-Renewal
  200. Promoter hypermethylation of the phosphatase DUSP22 mediates PKA‐dependent TAU phosphorylation and CREB activation in Alzheimer's disease
  201. Relationship between genome and epigenome - challenges and requirements for future research
  202. Synergy and competition between cancer genome sequencing and epigenome mapping projects
  203. Somatic Mutations of Calreticulin in Myeloproliferative Neoplasms
  204. A Prognostic DNA Methylation Signature for Stage I Non–Small-Cell Lung Cancer
  205. Complex Patterns of Chromosome 11 Aberrations in Myeloid Malignancies Target CBL, MLL, DDB1 and LMO2
  206. Recommendations for the design and analysis of epigenome-wide association studies
  207. A reversible gene trap collection empowers haploid genetics in human cells
  208. A Kinase-Independent Function of CDK6 Links the Cell Cycle to Tumor Angiogenesis
  209. Identification of Novel Imprinted Differentially Methylated Regions by Global Analysis of Human-Parthenogenetic-Induced Pluripotent Stem Cells
  210. High-Resolution Mapping of H1 Linker Histone Variants in Embryonic Stem Cells
  211. Proliferation-Dependent Alterations of the DNA Methylation Landscape Underlie Hematopoietic Stem Cell Aging
  212. DNA methylation: a matter of culture
  213. Comparative genome-wide DNA methylation analysis of colorectal tumor and matched normal tissues
  214. Analysing and interpreting DNA methylation data
  215. DNA Methylation Dynamics during In Vivo Differentiation of Blood and Skin Stem Cells
  216. Managing drug resistance in cancer: lessons from HIV therapy
  217. DNA methylation biomarkers in cancer: progress towards clinical implementation
  218. Erosion of Dosage Compensation Impacts Human iPSC Disease Modeling
  219. Sequential ChIP-bisulfite sequencing enables direct genome-scale investigation of chromatin and DNA methylation cross-talk
  220. BLUEPRINT to decode the epigenetic signature written in blood
  221. Epigenom-Karten erstellen und nutzen
  222. EpiExplorer: live exploration and global analysis of large epigenomic datasets
  223. Analyzing Epigenome Data in Context of Genome Evolution and Human Diseases
  224. Genomic Distribution and Inter-Sample Variation of Non-CpG Methylation across Human Cell Types
  225. RRBSMAP: a fast, accurate and user-friendly alignment tool for reduced representation bisulfite sequencing
  226. Dnmt3a is essential for hematopoietic stem cell differentiation
  227. Global DNA Demethylation During Mouse Erythropoiesis in Vivo
  228. Highly efficient derivation of ventricular cardiomyocytes from induced pluripotent stem cells with a distinct epigenetic signature
  229. A promoter DNA demethylation landscape of human hematopoietic differentiation
  230. Lung Stem Cell Self-Renewal Relies on BMI1-Dependent Control of Expression at Imprinted Loci
  231. A DNA methylation fingerprint of 1628 human samples
  232. BiQ Analyzer HT: locus-specific analysis of DNA methylation by high-throughput bisulfite sequencing
  233. Preparation of reduced representation bisulfite sequencing libraries for genome-scale DNA methylation profiling
  234. Reference Maps of Human ES and iPS Cell Variation Enable High-Throughput Characterization of Pluripotent Cell Lines
  235. Paternally Induced Transgenerational Environmental Reprogramming of Metabolic Gene Expression in Mammals
  236. Comparison of sequencing-based methods to profile DNA methylation and identification of monoallelic epigenetic modifications
  237. Quantitative comparison of genome-wide DNA methylation mapping technologies
  238. Genome-scale DNA methylation mapping of clinical samples at single-nucleotide resolution
  239. Web-Based Analysis of (Epi-) Genome Data Using EpiGRAPH and Galaxy
  240. Epigenetic biomarker development
  241. High-throughput bisulfite sequencing in mammalian genomes
  242. DNA Methylation Analysis of Chromosome 21 Gene Promoters at Single Base Pair and Single Allele Resolution
  243. MethMarker: user-friendly design and optimization of gene-specific DNA methylation assays
  244. EpiGRAPH: user-friendly software for statistical analysis and prediction of (epi)genomic data
  245. IVF: stars may have to consider the risk of stolen parenthood
  246. Functional Analysis of a Potassium-Chloride Co-Transporter 3 (SLC12A6) Promoter Polymorphism Leading to an Additional DNA Methylation Site
  247. Inter-individual variation of DNA methylation and its implications for large-scale epigenome mapping
  248. Structural conservation versus functional divergence of maternally expressed microRNAs in the Dlk1/Gtl2 imprinting region
  249. Computational epigenetics
  250. Optimization of Quantitative MGMT Promoter Methylation Analysis Using Pyrosequencing and Combined Bisulfite Restriction Analysis
  251. The Human Genomic Melting Map
  252. CpG Island Mapping by Epigenome Prediction
  253. CpG Island Methylation in Human Lymphocytes Is Highly Correlated with DNA Sequence, Repeats, and Predicted DNA Structure
  254. BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing