Qiagen drug

External links

DrugBank · PubChem

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Mentioned in (34)

Papers in which this entity is mentioned.

• Whole-genome landscapes of 1,364 breast cancers. (2026)
• Rapid brain tumor classification from sparse epigenomic data. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Sequence modeling and design from molecular to genome scale with Evo. (2024)
• ESPRESSO: Robust discovery and quantification of transcript isoforms from error-prone long-read RNA-seq data. (2023)
• Massively parallel reporter perturbation assays uncover temporal regulatory architecture during neural differentiation. (2022)
• Single-cell genomic variation induced by mutational processes in cancer. (2022)
• Inferring gene expression from cell-free DNA fragmentation profiles. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress. (2021)
• B cells and tertiary lymphoid structures promote immunotherapy response. (2020)
• Immuno-genomic landscape of osteosarcoma. (2020)
• ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
• Hypermethylation of Proopiomelanocortin and Period 2 Genes in Blood Are Associated with Greater Subjective and Behavioral Motivation for Alcohol in Humans. (2019)
• Genetic compensation triggered by mutant mRNA degradation. (2019)
• Mutational processes shape the landscape of TP53 mutations in human cancer. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
• Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
• The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
• Fragment Length of Circulating Tumor DNA. (2016)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• ENVE: a novel computational framework characterizes copy-number mutational landscapes in colorectal cancers from African American patients. (2015)
• Clinical exome performance for reporting secondary genetic findings. (2015)
• Robust enumeration of cell subsets from tissue expression profiles. (2015)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. (2014)
• A simple consensus approach improves somatic mutation prediction accuracy. (2013)
• Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
• Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition. (2010)
• Splicing factor SFRS1 recognizes a functionally diverse landscape of RNA transcripts. (2009)
• Rapid SNP discovery and genetic mapping using sequenced RAD markers. (2008)

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