Latest

• Subpar reporting of pre‐analytical variables in RNA‐focused blood plasma studies
• Exploring the cell-free total RNA transcriptome in diffuse large B-cell lymphoma and primary mediastinal B-cell lymphoma patients as biomarker source in blood plasma liquid biopsies
• Large-scale benchmarking of circRNA detection tools reveals large differences in sensitivity but not in precision
• Patient-specific alterations in blood plasma cfRNA profiles enable accurate classification of cancer patients and controls
• Blocking Abundant RNA Transcripts by High-Affinity Oligonucleotides during Transcriptome Library Preparation
• RNA Extraction Method Impacts Quality Metrics and Sequencing Results in Formalin-Fixed, Paraffin-Embedded Tissue Samples
• Digital PCR-based evaluation of nucleic acid extraction kit performance for the co-purification of cell-free DNA and RNA
• Performance evaluation of RNA purification kits and blood collection tubes in the Extracellular RNA Quality Control (exRNAQC) study
• Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models enables specific monitoring of tumour-derived extracellular RNA
• mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel, and secondary fusion transcripts in FFPE tissue: a sarcoma showcase
• A 3′‐end capture sequencing method for high‐throughput targeted gene expression profiling
• RNA biomarkers from proximal liquid biopsy for diagnosis of ovarian cancer
• Validation of Circular RNAs Using RT‐qPCR After Effective Removal of Linear RNAs by Ribonuclease R
• Messenger RNA capture sequencing of extracellular RNA from human biofluids using a comprehensive set of spike-in controls
• Charting Extracellular Transcriptomes in The Human Biofluid RNA Atlas
• Performance assessment of total RNA sequencing of human biofluids and extracellular vesicles
• Charting extracellular transcriptomes in The Human Biofluid RNA Atlas
• Methyl-CpG-binding domain sequencing reveals a prognostic methylation signature in neuroblastoma
• Targeted resequencing and variant validation using pxlence PCR assays