Publisher Correction: Discovery of coding regions in the human genome by integrated proteogenomics analysis workflow

Published on Dec 1, 2018in Nature Communications11.878
· DOI :10.1038/s41467-018-04279-5
Yafeng Zhu7
Estimated H-index: 7
(Science for Life Laboratory),
Lukas M. Orre10
Estimated H-index: 10
(Science for Life Laboratory)
+ 6 AuthorsJanne Lehtiö38
Estimated H-index: 38
(Science for Life Laboratory)
In the original version of this Article, extraneous text not belonging to the Article was accidentally appended to the results section. This error has now been corrected in both the PDF and HTML versions of the Article.
  • References (0)
  • Citations (0)
📖 Papers frequently viewed together
51 Authors (Francesc Coll, ..., Taane G. Clark)
5 Citations
78% of Scinapse members use related papers. After signing in, all features are FREE.
Cited By0
#1Xiaoxue Tong (HUST: Huazhong University of Science and Technology)H-Index: 3
#2Xu Hong (HUST: Huazhong University of Science and Technology)H-Index: 3
Last. Shiyong Liu (HUST: Huazhong University of Science and Technology)H-Index: 13
view all 4 authors...
In recent years, researchers have discovered thousands of sORFs that can encode micropeptides, and more and more discoveries that non-AUG codons can be used as translation initiation sites for these micropeptides. On the basis of our previous tool CPPred, we develop CPPred-sORF by adding two features and using non-AUG as the starting codon, which makes a comprehensive evaluation of sORF. The database of CPPred-sORF are constructed by small coding RNA and lncRNA as positive and negative data, res...
#1Yan Zhou Tran (KI: Karolinska Institutet)H-Index: 1
#2Rezan Minozada (KI: Karolinska Institutet)
Last. Lukas M. Orre (KI: Karolinska Institutet)H-Index: 10
view all 7 authors...
Drug resistance is a major obstacle to curative cancer therapies, and increased understanding of the molecular events contributing to resistance would enable better prediction of therapy response, as well as contribute to new targets for combination therapy. Here we have analyzed the early molecular response to epidermal growth factor receptor (EGFR) inhibition using RNA sequencing data covering 13 486 genes and mass spectrometry data covering 10 138 proteins. This analysis revealed a massive re...
#1Rubin N. Joshi (Science for Life Laboratory)H-Index: 2
#2Charlotte Stadler (KTH: Royal Institute of Technology)H-Index: 10
Last. Mattias Vesterlund (Science for Life Laboratory)H-Index: 12
view all 7 authors...
We have curated an in-depth subcellular proteomic map of primary human CD4+ T cells, divided into cytosolic, nuclear and membrane fractions generated by an optimized fractionation and HiRIEF-LC-MS/MS workflow for limited amounts of primary cells. The subcellular proteome of T cells was mapped under steady state conditions, as well as upon 15 minutes and 1 hour of T cell receptor (TCR) stimulation respectively. We quantified the subcellular distribution of 6572 proteins and identified a subset of...