Illumina HiSeq 2000 drug

Aliases: HiSeq 2000
External links: DrugBank · PubChem

Evidence from: primary | all sources

Related entities (3)

Subject	Relation	Object	p-value	Evidence
Illumina HiSeq 2000	associated_with	RNA	—	1
LDACC	interacts_with	Illumina HiSeq 2000	—	1
Tn5 transposase	associated_with	Illumina HiSeq 2000	—	1

Mentioned in (39)

Papers in which this entity is mentioned.

Transient loss of Polycomb components induces an epigenetic cancer fate. (2024)
De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder. (2019)
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)
Failed Progenitor Specification Underlies the Cardiopharyngeal Phenotypes in a Zebrafish Model of 22q11.2 Deletion Syndrome. (2018)
Orthotopic patient-derived xenografts of paediatric solid tumours. (2017)
De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
Impact of cytosine methylation on DNA binding specificities of human transcription factors. (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)
De novo variants in sporadic cases of childhood onset schizophrenia. (2016)
Experience-Dependent Accumulation of N6-Methyladenosine in the Prefrontal Cortex Is Associated with Memory Processes in Mice. (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)
GABRA2 Alcohol Dependence Risk Allele is Associated with Reduced Expression of Chromosome 4p12 GABAA Subunit Genes in Human Neural Cultures. (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)
Identification of the genomic insertion site of Pmel-1 TCR α and β transgenes by next-generation sequencing. (2014)
A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium. (2014)
708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
Distinct structural transitions of chromatin topological domains correlate with coordinated hormone-induced gene regulation. (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 Genotype-Tissue Expression (GTEx) project. (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)
A promoter polymorphism in the Per3 gene is associated with alcohol and stress response. (2012)
Accurate and comprehensive sequencing of personal genomes. (2011)

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
illumina hiseq 2000	drug	28	35
hiseq 2000	drug	13	21