cDNA drug

Aliases

complementary DNA, second strand cDNA

External links

DrugBank · PubChem

No related entities found.

Mentioned in (50)

Papers in which this entity is mentioned.

• Single-cell exon deletion profiling reveals splicing events that shape gene expression and cell state dynamics. (2026)
• Tumour-wide RNA splicing aberrations generate actionable public neoantigens. (2025)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• Massively parallel reporter assay investigates shared genetic variants of eight psychiatric disorders. (2025)
• Multiple overlapping binding sites determine transcription factor occupancy. (2025)
• Integrated single-cell multiomic profiling of caudate nucleus suggests key mechanisms in alcohol use disorder. (2025)
• Single cell and spatial alternative splicing analysis with Nanopore long read sequencing. (2025)
• Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
• Alternative splicing of transcript mediates the response of circadian clocks to temperature changes. (2024)
• The Application of Long-Read Sequencing to Cancer. (2024)
• Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
• ESPRESSO: Robust discovery and quantification of transcript isoforms from error-prone long-read RNA-seq data. (2023)
• Nanopore sequencing of RNA and cDNA molecules in . (2022)
• Nanopore sequencing technology, bioinformatics and applications. (2021)
• Application of third-generation sequencing in cancer research. (2021)
• Alternative splicing: Human disease and quantitative analysis from high-throughput sequencing. (2021)
• Joint single-cell measurements of nuclear proteins and RNA in vivo. (2021)
• Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
• Effects of chronic intermittent ethanol exposure and withdrawal on neuroblastoma cell transcriptome. (2020)
• Transcriptomic signatures across human tissues identify functional rare genetic variation. (2020)
• Single-Cell RNA-Seq Reveals AML Hierarchies Relevant to Disease Progression and Immunity. (2019)
• The role and robustness of the Gini coefficient as an unbiased tool for the selection of Gini genes for normalising expression profiling data. (2019)
• Persistent Changes in Stress-Regulatory Genes in Pregnant Women or Children Exposed Prenatally to Alcohol. (2019)
• Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma. (2019)
• Sequence, Structure, and Context Preferences of Human RNA Binding Proteins. (2018)
• PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites. (2018)
• ChimeRScope: a novel alignment-free algorithm for fusion transcript prediction using paired-end RNA-Seq data. (2017)
• Integrated analysis of gene expression and copy number identified potential cancer driver genes with amplification-dependent overexpression in 1,454 solid tumors. (2017)
• Preaxial polydactyly following early gestational exposure to the smoothened agonist, SAG, in C57BL/6J mice. (2017)
• Alternative Polyadenylation Directs Tissue-Specific miRNA Targeting in Somatic Tissues. (2017)
• A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications. (2017)
• Interaction of glycosphingolipids GD3 and GD2 with growth factor receptors maintains breast cancer stem cell phenotype. (2017)
• PGBD5 promotes site-specific oncogenic mutations in human tumors. (2017)
• The Ensembl gene annotation system. (2016)
• Three decades of nanopore sequencing. (2016)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• Spatial reconstruction of single-cell gene expression data. (2015)
• Design and bioinformatics analysis of genome-wide CLIP experiments. (2015)
• Position-specific binding of FUS to nascent RNA regulates mRNA length. (2015)
• Comprehensive genomic profiles of small cell lung cancer. (2015)
• The future of DNA sequence archiving. (2012)
• Circular RNAs are the predominant transcript isoform from hundreds of human genes in diverse cell types. (2012)
• HLA typing from RNA-Seq sequence reads. (2012)
• Effects of ethanol and NAP on cerebellar expression of the neural cell adhesion molecule L1. (2011)
• Integrative analysis of the melanoma transcriptome. (2010)
• POLYAR, a new computer program for prediction of poly(A) sites in human sequences. (2010)
• Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. (2010)
• Computation for ChIP-seq and RNA-seq studies. (2009)
• RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. (2008)
• A large-scale analysis of mRNA polyadenylation of human and mouse genes. (2005)

Merged raw entities (3)

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