2017
DOI: 10.1093/nar/gkx1098
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Ensembl 2018

Abstract: The Ensembl project has been aggregating, processing, integrating and redistributing genomic datasets since the initial releases of the draft human genome, with the aim of accelerating genomics research through rapid open distribution of public data. Large amounts of raw data are thus transformed into knowledge, which is made available via a multitude of channels, in particular our browser (http://www.ensembl.org). Over time, we have expanded in multiple directions. First, our resources describe multiple field… Show more

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Cited by 2,589 publications
(2,363 citation statements)
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References 37 publications
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“…Pokorná et al, 2011;O'Meally et al, 2012]. We performed BLAST of the assembled female-specific RAD contigs to the chicken transcriptome (using Ensembl [Zerbino et al, 2018]), implemented in Geneious (v10) [Kearse et al, 2012] with a maximum E-value cutoff of 1e -50 and word size of 15 bp.…”
Section: Using the Qiagenmentioning
confidence: 99%
“…Pokorná et al, 2011;O'Meally et al, 2012]. We performed BLAST of the assembled female-specific RAD contigs to the chicken transcriptome (using Ensembl [Zerbino et al, 2018]), implemented in Geneious (v10) [Kearse et al, 2012] with a maximum E-value cutoff of 1e -50 and word size of 15 bp.…”
Section: Using the Qiagenmentioning
confidence: 99%
“…It is desirable to test and apply our method on the data from other sources. We therefore searched for the relevant data from other databases including Gene Expression Omnibus (GEO) [62], Ensembl [63], Hugo Gene Nomenclature Committee (HGNC) [64], ArrayExpress [65], and Catalogue of Somatic Mutations in Cancer (COSMIC) [66]. These databases provide comprehensive genome data for colon cancer, such as gene expression dataset, somatic mutation dataset and gene location dataset even gene Methylation dataset.…”
Section: Discussionmentioning
confidence: 99%
“…iORF aligned coordinates were then converted to genomic coordinates on the respective genomes of each strain, and removed if there was any overlap with a known feature annotation, such as rRNA, a tRNA, a ncRNA, a snoRNA, non-conserved genes and pseudogenes annotated on the reference S288C (version R64-2-1 https://www.yeastgenome.org/). Additional masking was performed by removing iORFs i) located in a region with more than 0.6 % of sequence identity with S. cerevisiae ncRNA or gene (including pseudogenes and excluding dubious ORFs) from the reference genome, or Saccharomyces kudriavzevii and Saccharomyces eubayanus genes (Zerbino et al 2018), ii) in a low complexity region identified with repeat masker (http://www.repeatmasker.org/) and iii) when local alignments of iORFs +/-300 bp displayed less than 60% of identity (including gaps). If an .…”
Section: Iorf Annotation and Conservation Levelmentioning
confidence: 99%