PCR drug

Aliases

Eighteen cycles of PCR, polymerase chain reaction, qPCR, random priming PCR, real-time PCR

External links

DrugBank · PubChem

No related entities found.

Mentioned in (39)

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)
• 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)
• 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)
• 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)
• 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)
• 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)
• A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. (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)
• 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)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• The HLA system: genetics, immunology, clinical testing, and clinical implications. (2007)
• Rapid Sex Determination Using PCR Technique Compared to Classic Cytogenetics - PMC

Merged raw entities (5)

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