normal goat serum drug

Aliases

NGS, goat serum, normal goat serum

External links

DrugBank · PubChem

Related entities (1)

Mentioned in (29)

Papers in which this entity is mentioned.

• Tracing the evolution of single-cell 3D genomes in Kras-driven cancers. (2025)
• MYC ecDNA promotes intratumour heterogeneity and plasticity in PDAC. (2025)
• Tumor-informed deep sequencing of ctDNA detects minimal residual disease and predicts relapse in osteosarcoma. (2024)
• Machine-guided design of cell-type-targeting cis-regulatory elements. (2024)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• The Application of Long-Read Sequencing to Cancer. (2024)
• Embryonic ethanol exposure disrupts craniofacial neuromuscular integration in zebrafish larvae. (2023)
• Alcohol reverses the effects of KCNJ6 (GIRK2) noncoding variants on excitability of human glutamatergic neurons. (2023)
• Application of third-generation sequencing in cancer research. (2021)
• Detection of somatic structural variants from short-read next-generation sequencing data. (2021)
• Joint single-cell measurements of nuclear proteins and RNA in vivo. (2021)
• Prenatal alcohol exposure disrupts Sonic hedgehog pathway and primary cilia genes in the mouse neural tube. (2021)
• Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
• Differential sensitivity of human neurons carrying μ opioid receptor (MOR) N40D variants in response to ethanol. (2020)
• The evolution of tumour phylogenetics: principles and practice. (2017)
• 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)
• FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing. (2016)
• Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
• HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
• VariantDB: a flexible annotation and filtering portal for next generation sequencing data. (2014)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• Diminishing return for increased Mappability with longer sequencing reads: implications of the k-mer distributions in the human genome. (2014)
• Effects of one- and three-day binge alcohol exposure in neonatal C57BL/6 mice on spatial learning and memory in adolescence and adulthood. (2014)
• Rapid genome mapping in nanochannel arrays for highly complete and accurate de novo sequence assembly of the complex Aegilops tauschii genome. (2013)
• ACMG clinical laboratory standards for next-generation sequencing. (2013)
• cn.MOPS: mixture of Poissons for discovering copy number variations in next-generation sequencing data with a low false discovery rate. (2012)
• AID/APOBEC cytosine deaminase induces genome-wide kataegis. (2012)
• HLA typing from RNA-Seq sequence reads. (2012)
• The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. (2010)

Merged raw entities (3)

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