Evidence map›Paper›PMID 29889196›Full record

ArticleJournal of visualized experiments : JoVE2018

A Fast and Quantitative Method for Post-translational Modification and Variant Enabled Mapping of Peptides to Genomes.

Christoph N Schlaffner, Georg J Pirklbauer, Andreas Bender, Judith A J Steen, Jyoti S Choudhary

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In one paragraph

Article in Journal of visualized experiments : JoVE, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Christoph N SchlaffnerDepartment of Neurobiology, F. M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School; Proteomic Mass Spectrometry, Wellcome Trust Sanger Institute, Wellcome Genome Campus; Centre for Molecular Informatics, Department of Chemistry, University of Cambridge; christoph.schlaffner@childrens.harvard.edu.
Georg J PirklbauerProteomic Mass Spectrometry, Wellcome Trust Sanger Institute, Wellcome Genome Campus.
Andreas BenderCentre for Molecular Informatics, Department of Chemistry, University of Cambridge.
Judith A J SteenDepartment of Neurobiology, F. M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School.
Jyoti S ChoudharyProteomic Mass Spectrometry, Wellcome Trust Sanger Institute, Wellcome Genome Campus; Functional Proteomics Group, Chester Beatty Laboratories, Institute of Cancer Research.

Funding

GENCODE Resource ProjectU41HG007234 · NHGRI · SANGER INSTITUTE · PI FLICEK, PAUL · 2013 to 2020
$20.3M
NHGRI NIH HHS U41 HG007234Wellcome TrustWellcome Trust WT098051
6 · The paper itself

Abstract

Cross-talk between genes, transcripts, and proteins is the key to cellular responses; hence, analysis of molecular levels as distinct entities is slowly being extended to integrative studies to enhance the understanding of molecular dynamics within cells. Current tools for the visualization and integration of proteomics with other omics datasets are inadequate for large-scale studies. Furthermore, they only capture basic sequence identify, discarding post-translational modifications and quantitation. To address these issues, we developed PoGo to map peptides with associated post-translational modifications and quantification to reference genome annotation. In addition, the tool was developed to enable the mapping of peptides identified from customized sequence databases incorporating single amino acid variants. While PoGo is a command line tool, the graphical interface PoGoGUI enables non-bioinformatics researchers to easily map peptides to 25 species supported by Ensembl genome annotation. The generated output borrows file formats from the genomics field and, therefore, visualization is supported in most genome browsers. For large-scale studies, PoGo is supported by TrackHubGenerator to create web-accessible repositories of data mapped to genomes that also enable an easy sharing of proteogenomics data. With little effort, this tool can map millions of peptides to reference genomes within only a few minutes, outperforming other available sequence-identity based tools. This protocol demonstrates the best approaches for proteogenomics mapping through PoGo with publicly available datasets of quantitative and phosphoproteomics, as well as large-scale studies.

Indexed as

GenomeGenomicsPeptidesProtein Processing, Post-TranslationalProteomicsPeptides

Identifiers

PMID29889196
PMCPMC6101353

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.