Evidence map›Paper›PMID 26657539›Full record

ArticleMolecular & cellular proteomics : MCP2016

proBAMsuite, a Bioinformatics Framework for Genome-Based Representation and Analysis of Proteomics Data.

Xiaojing Wang, Robbert J C Slebos, Matthew C Chambers, David L Tabb, Daniel C Liebler, Bing Zhang

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. How many human proteoforms are there?Nature chemical biology · 2018
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Methods, Tools and Current Perspectives in Proteogenomics.Molecular & cellular proteomics : MCP · 2017
    Review
  11. Article
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

6 authors.

Xiaojing WangFrom the ‡Department of Biomedical Informatics.
Robbert J C Slebos§Department of Biochemistry, ¶Jim Ayers Institute for Precancer Detection and Diagnosis, Vanderbilt-Ingram Cancer Center, Nashville, TN 37232.
Matthew C ChambersFrom the ‡Department of Biomedical Informatics.
David L TabbFrom the ‡Department of Biomedical Informatics, §Department of Biochemistry.
Daniel C LieblerFrom the ‡Department of Biomedical Informatics, §Department of Biochemistry, ¶Jim Ayers Institute for Precancer Detection and Diagnosis, Vanderbilt-Ingram Cancer Center, Nashville, TN 37232.
Bing ZhangFrom the ‡Department of Biomedical Informatics, ‖Department of Cancer Biology, Vanderbilt University School of Medicine, Nashville, TN 37232; bing.zhang@vanderbilt.edu.

Funding

Vanderbilt Proteome Characterization CenterU24CA159988 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI LIEBLER, DANIEL C · 2011 to 2016
$13.9M
NCI NIH HHS U24 CA159988NCI NIH HHS U24CA159988
6 · The paper itself

Abstract

To facilitate genome-based representation and analysis of proteomics data, we developed a new bioinformatics framework, proBAMsuite, in which a central component is the protein BAM (proBAM) file format for organizing peptide spectrum matches (PSMs)(1) within the context of the genome. proBAMsuite also includes two R packages, proBAMr and proBAMtools, for generating and analyzing proBAM files, respectively. Applying proBAMsuite to three recently published proteomics datasets, we demonstrated its utility in facilitating efficient genome-based sharing, interpretation, and integration of proteomics data. First, the interpretation of proteomics data is significantly enhanced with the rich genomic annotation information. Second, PSMs can be easily reannotated using user-specified gene annotation schemes and assembled into both protein and gene identifications. Third, using the genome as a common reference, proBAMsuite facilitates seamless proteomics and proteogenomics data integration. Finally, proBAM files can be readily visualized in genome browsers and thus bring proteomics data analysis to a general audience beyond the proteomics community. Results from this study establish proBAMsuite as a useful bioinformatics framework for proteomics and proteogenomics research.

Indexed as

Molecular Sequence AnnotationBcl-2-Like Protein 11Computational BiologyDatabases, ProteinGenome, HumanHumansPeptidesProteomicsSequence Analysis, DNAWeb BrowserBcl-2-Like Protein 11Peptides

Identifiers

PMID26657539
PMCPMC4813696

What OpenQuestion holds

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LicenceCC BY
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.