Searching journal content for articles similar to Farrell et al. 32 (1): 175.

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  1. ...(Gatta and Mantovani 2011). 1196 Genome Research www..org Fleming et al. NF-Y binds to a diverse set of genomic features including nongenic regions We annotated the NF-Y bound regions in K562 to RefSeq genes, TSSs, maps of histone modifications and nucleosome-depleted regions, and RNA levels...
  2. ...of our experimentally determined nTARs and compared it with the positive signals overlapping with RefSeq exons. In terms of conservation, as expected, expressed regions corresponding to RefSeq exons showed a substantial level of conservation with a median phastCons score of 0.425, whereas the majority...
  3. ...Corresponding authors: vakirlis@fleming.gr, anne.kupczok@wur.nlAbstractSpecies-specific genes, also known as orphans, are ubiquitous across life's domains. In prokaryotes, species-specific orphan genes (SSOGs) are mostly thought to originate in external elements such as viruses followed by horizontal gene...
  4. ...of novel human PTES transcripts As part of a pilot screen for novel splice variants and fusion genes within cancer s, a total of 9.7 Gb of Illumina and 454 Life Sciences (Roche) FLX sequence data was generated from seven human pediatric tumor samples and one cell line and was mapped to the RefSeq gene set...
  5. ...2010). The number of reads mapped to the exons of each RefSeq genewas calculated, and the corresponding RPKM (reads mapping to the per kilobase of transcript per million reads obtained fromsequencing) valuewas derived (SupplementalMaterial Section 3). Statistical analysis of differentially expressed...
  6. .... There are several large-scale gene annotation projects in progress on the human , including RefSeq (Pruitt et al. 2005), GENCODE (Harrow et al. 2012), andUCSCGenes (Dreszer et al. 2012). In each ‘‘gene set’’ or ‘‘genebuild’’ produced, the vast majority of models are based upon transcriptomics data. Briefly, GENCODE...
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  7. ...obtained from the UCSC Genome Browser database ( http://.cse.ucsc.edu/ ). The human NCBI33 (hg15, April 2003) assembly was used. The NCBI Reference Sequence (RefSeq; http://www.ncbi.nlm.nih.gov/RefSeq/ ) transcript coordinates were taken from the UCSC database refGenes.txt file. Coordinates of the EST...
  8. ...equally to this work. Abstract Trans -splicing is a post-transcriptional event that joins exons from separate pre-mRNAs. Detection of trans -splicing is usually severely hampered by experimental artifacts and genetic rearrangements. Here, we develop a new computational pipeline, TSscan, which...
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