PCR drug
Evidence from:
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all sources
Related entities (8)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| Agilent 2100 Bioanalyzer | associated_with | PCR | — | 1 |
| DNA | interacts_with | PCR | — | 1 |
| DNA | regulates | PCR | — | 1 |
| PCR | interacts_with | cDNA | — | 1 |
| PCR | associated_with | depression | — | 1 |
| PCR | interacts_with | DNA | — | 1 |
| PCR | interacts_with | genomic DNA | — | 1 |
| PCR | associated_with | schizophrenia | — | 1 |
Mentioned in (58)
Papers in which this entity is mentioned.
- Microfluidic purification of genomic DNA. (2025)
- Multiple overlapping binding sites determine transcription factor occupancy. (2025)
- Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
- A harmonized public resource of deeply sequenced diverse human genomes. (2024)
- H-MRS neurometabolite profiles and motor development in school-aged children who are HIV-exposed uninfected: a birth cohort study. (2023)
- A Neurometabolic Pattern of Elevated Myo-Inositol in Children Who Are HIV-Exposed and Uninfected: A South African Birth Cohort Study. (2022)
- At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
- Cell-free DNA technologies for the analysis of brain cancer. (2022)
- Detection and characterization of lung cancer using cell-free DNA fragmentomes. (2021)
- Accurate detection of circulating tumor DNA using nanopore consensus sequencing. (2021)
- Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
- UMI-linked consensus sequencing enables phylogenetic analysis of directed evolution. (2020)
- Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring. (2020)
- Pan-cancer analysis of whole genomes. (2020)
- An interaction between fetal sex and placental weight and efficiency predicts intrauterine growth in response to maternal protein insufficiency and gestational exposure window in a mouse model of FASD. (2020)
- Early child development in children who are HIV-exposed uninfected compared to children who are HIV-unexposed: observational sub-study of a cluster-randomized trial in rural Zimbabwe. (2020)
- Genetic compensation triggered by mutant mRNA degradation. (2019)
- CUT&RUNTools: a flexible pipeline for CUT&RUN processing and footprint analysis. (2019)
- Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. (2018)
- Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
- Statistical algorithms improve accuracy of gene fusion detection. (2017)
- Assembly of functionally integrated human forebrain spheroids. (2017)
- A practical guide to single-cell RNA-sequencing for biomedical research and clinical applications. (2017)
- Mapping and phasing of structural variation in patient genomes using nanopore sequencing. (2017)
- Impact of cytosine methylation on DNA binding specificities of human transcription factors. (2017)
- DNA Methylation Analysis: Choosing the Right Method. (2016)
- Fragment Length of Circulating Tumor DNA. (2016)
- A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. (2016)
- Three decades of nanopore sequencing. (2016)
- CONTRAILS: A tool for rapid identification of transgene integration sites in complex, repetitive genomes using low-coverage paired-end sequencing. (2015)
- limma powers differential expression analyses for RNA-sequencing and microarray studies. (2015)
- HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
- Position-specific binding of FUS to nascent RNA regulates mRNA length. (2015)
- The use of exome capture RNA-seq for highly degraded RNA with application to clinical cancer sequencing. (2015)
- Comprehensive genomic profiles of small cell lung cancer. (2015)
- Identification of the genomic insertion site of Pmel-1 TCR α and β transgenes by next-generation sequencing. (2014)
- Detecting ultralow-frequency mutations by Duplex Sequencing. (2014)
- Distribution, recognition and regulation of non-CpG methylation in the adult mammalian brain. (2014)
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. (2014)
- Quality of 186 child brain spectra using motion and B0 shim navigated single voxel spectroscopy. (2014)
- Gene expression signatures affected by alcohol-induced DNA methylomic deregulation in human embryonic stem cells. (2014)
- Comprehensive analysis of the transcriptional landscape of the human FMR1 gene reveals two new long noncoding RNAs differentially expressed in Fragile X syndrome and Fragile X-associated tremor/ataxia syndrome. (2014)
- A simple consensus approach improves somatic mutation prediction accuracy. (2013)
- The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
- Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
- VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)
- Summarizing and correcting the GC content bias in high-throughput sequencing. (2012)
- HLA typing from RNA-Seq sequence reads. (2012)
- Temporally- and spatially-regulated transcriptional activity of the nicotinic acetylcholine receptor beta4 subunit gene promoter. (2010)
- Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library. (2010)
- Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. (2010)
- Conserved role of intragenic DNA methylation in regulating alternative promoters. (2010)
- BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
- From mouse to man: the 5-HT3 receptor modulates physical dependence on opioid narcotics. (2009)
- Lack of association between the A118G polymorphism of the mu opioid receptor gene (OPRM1) and opioid dependence: A meta-analysis. (2009)
- The HLA system: genetics, immunology, clinical testing, and clinical implications. (2007)
- Genome-wide maps of chromatin state in pluripotent and lineage-committed cells. (2007)
- Rapid Sex Determination Using PCR Technique Compared to Classic Cytogenetics - PMC
Merged raw entities (5)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| pcr | drug | 55 | 69 |
| real-time pcr | drug | 3 | 3 |
| polymerase chain reaction | drug | 1 | 1 |
| eighteen cycles of pcr | drug | — | — |
| random priming pcr | drug | — | — |