qPCR drug
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| qPCR | interacts_with | ATAC-seq | — | 1 |
| qPCR | targets | CNV | — | 1 |
| qPCR | interacts_with | de novo variant | — | 1 |
Mentioned in (24)
Papers in which this entity is mentioned.
- Extrachromosomal DNA-Driven Oncogene Spatial Heterogeneity and Evolution in Glioblastoma. (2025)
- Micro-RNA-125a mediates the effects of hypomethylating agents in chronic myelomonocytic leukemia. (2021)
- Failed Progenitor Specification Underlies the Cardiopharyngeal Phenotypes in a Zebrafish Model of 22q11.2 Deletion Syndrome. (2018)
- An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
- Estimating the population abundance of tissue-infiltrating immune and stromal cell populations using gene expression. (2016)
- CONTRAILS: A tool for rapid identification of transgene integration sites in complex, repetitive genomes using low-coverage paired-end sequencing. (2015)
- ENVE: a novel computational framework characterizes copy-number mutational landscapes in colorectal cancers from African American patients. (2015)
- ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide. (2015)
- Long Noncoding RNA-Directed Epigenetic Regulation of Gene Expression Is Associated With Anxiety-like Behavior in Mice. (2015)
- Detecting ultralow-frequency mutations by Duplex Sequencing. (2014)
- A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. (2014)
- Estimating telomere length from whole genome sequence data. (2014)
- An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. (2014)
- Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice. (2013)
- Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
- High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
- Assessing telomeric DNA content in pediatric cancers using whole-genome sequencing data. (2012)
- Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. (2011)
- Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion. (2011)
- Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn. (2011)
- DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing. (2010)
- Role of Tet proteins in 5mC to 5hmC conversion, ES-cell self-renewal and inner cell mass specification. (2010)
- Chromatin immunoprecipitation (ChIP) coupled to detection by quantitative real-time PCR to study transcription factor binding to DNA in Caenorhabditis elegans. (2008)
- Accurate and reliable high-throughput detection of copy number variation in the human genome. (2006)
Merged raw entities (2)
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 |
|---|---|---|---|
| qpcr | drug | 18 | 29 |
| quantitative pcr | drug | 7 | 8 |