Illumina HiSeq 2000 drug

Aliases

HiSeq 2000

External links

DrugBank · PubChem

No related entities found.

Mentioned in (26)

Papers in which this entity is mentioned.

• Transient loss of Polycomb components induces an epigenetic cancer fate. (2024)
• Circular DNA elements of chromosomal origin are common in healthy human somatic tissue. (2018)
• A fast detection of fusion genes from paired-end RNA-seq data. (2018)
• Genome-wide somatic variant calling using localized colored de Bruijn graphs. (2018)
• Positively selected enhancer elements endow osteosarcoma cells with metastatic competence. (2018)
• Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
• Orthotopic patient-derived xenografts of paediatric solid tumours. (2017)
• Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma. (2017)
• Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin. (2016)
• Estimating the population abundance of tissue-infiltrating immune and stromal cell populations using gene expression. (2016)
• Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
• ENVE: a novel computational framework characterizes copy-number mutational landscapes in colorectal cancers from African American patients. (2015)
• BET inhibitors induce apoptosis through a MYC independent mechanism and synergise with CDK inhibitors to kill osteosarcoma cells. (2015)
• Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. (2015)
• Comparison of RNA-seq and microarray-based models for clinical endpoint prediction. (2015)
• A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. (2014)
• OptiType: precision HLA typing from next-generation sequencing data. (2014)
• Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014)
• An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. (2014)
• Clinical whole-exome sequencing for the diagnosis of mendelian disorders. (2013)
• A simple consensus approach improves somatic mutation prediction accuracy. (2013)
• The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
• High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
• Accurate and comprehensive sequencing of personal genomes. (2011)

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