Evidence map›Paper›PMID 26653538›Full record

ArticleJournal of proteome research2016

Reproducibility of Differential Proteomic Technologies in CPTAC Fractionated Xenografts.

David L Tabb, Xia Wang, Steven A Carr, Karl R Clauser, Philipp Mertins, Matthew C Chambers, Jerry D Holman, Jing Wang, Bing Zhang, Lisa J Zimmerman and 25 more

Abstract read
In one paragraph

Article in Journal of proteome research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

35 authors.

David L Tabb
Xia WangDepartment of Mathematical Sciences, University of Cincinnati , Cincinnati, Ohio 45221, United States.
Steven A CarrProteomics Platform, Broad Institute of MIT and Harvard , Cambridge, Massachusetts 02142, United States.
Karl R ClauserProteomics Platform, Broad Institute of MIT and Harvard , Cambridge, Massachusetts 02142, United States.
Philipp MertinsProteomics Platform, Broad Institute of MIT and Harvard , Cambridge, Massachusetts 02142, United States.
Matthew C Chambers
Jerry D Holman
Jing Wang
Bing Zhang
Lisa J Zimmerman
Xian ChenDepartment of Biochemistry and Biophysics, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
Harsha P GunawardenaDepartment of Biochemistry and Biophysics, University of North Carolina , Chapel Hill, North Carolina 27599, United States.
Sherri R DaviesDepartment of Medicine, Washington University , St. Louis, Missouri 63110, United States.
Matthew J C EllisDepartment of Medicine, Washington University , St. Louis, Missouri 63110, United States.
Shunqiang LiDepartment of Medicine, Washington University , St. Louis, Missouri 63110, United States.
R Reid TownsendDepartment of Medicine, Washington University , St. Louis, Missouri 63110, United States.
Emily S BojaOffice of Cancer Clinical Proteomics Research, National Cancer Institute , Bethesda, Maryland 20892, United States.
Karen A KetchumEnterprise Science and Computing, Inc. , Rockville, Maryland 20850, United States.
Christopher R KinsingerOffice of Cancer Clinical Proteomics Research, National Cancer Institute , Bethesda, Maryland 20892, United States.
Mehdi MesriOffice of Cancer Clinical Proteomics Research, National Cancer Institute , Bethesda, Maryland 20892, United States.
Henry RodriguezOffice of Cancer Clinical Proteomics Research, National Cancer Institute , Bethesda, Maryland 20892, United States.
Tao LiuDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Sangtae KimDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Jason E McDermottDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Samuel H PayneDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Vladislav A PetyukDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Karin D RodlandDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Richard D SmithDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Feng YangDivision of Biological Sciences, Pacific Northwest National Laboratory , Richland, Washington 99352, United States.
Daniel W ChanJHMI and Division of Clinical Chemistry, Johns Hopkins University , Baltimore, Maryland 21231, United States.
Bai ZhangJHMI and Division of Clinical Chemistry, Johns Hopkins University , Baltimore, Maryland 21231, United States.
Hui ZhangJHMI and Division of Clinical Chemistry, Johns Hopkins University , Baltimore, Maryland 21231, United States.
Zhen ZhangJHMI and Division of Clinical Chemistry, Johns Hopkins University , Baltimore, Maryland 21231, United States.
Jian-Ying ZhouJHMI and Division of Clinical Chemistry, Johns Hopkins University , Baltimore, Maryland 21231, United States.
Daniel C Liebler

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University Institute of Clinical and Translational Sciences (UL1)UL1RR024992 · NCRR · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2007 to 2011
$45.4M
Washington University Institute of Clinical and Translational SciencesUL1TR000448 · NCATS · WASHINGTON UNIVERSITY · PI EVANOFF, BRADLEY A · 2012 to 2016
$41.4M
Proteo-genomic Discovery, Prioritization and Verification of Cancer BiomarkersU24CA160034 · NCI · BROAD INSTITUTE, INC. · PI CARR, STEVEN A, PAULOVICH, AMANDA G · 2011 to 2016
$16.2M
PNNL Clinical Proteome Characterization CenterU24CA160019 · NCI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI RODLAND, KARIN D, SMITH, RICHARD D · 2011 to 2016
$15.7M
Vanderbilt Proteome Characterization CenterU24CA159988 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI LIEBLER, DANIEL C · 2011 to 2016
$13.9M
Cancer Proteome Center at Washington Univ, Univ of North Carolina & Boise StateU24CA160035 · NCI · WASHINGTON UNIVERSITY · PI CHEN, XIAN, ELLIS, MATTHEW J · 2011 to 2016
$11.8M
Proteome Characterization Center: A Genoproteomics Pipeline for Cance ResearchU24CA160036 · NCI · JOHNS HOPKINS UNIVERSITY · PI CHAN, DANIEL WANYUI, ZHANG, HUI · 2011 to 2016
$10.7M
NCATS NIH HHS UL1 TR000448NCI NIH HHS HHSN261201100106CNCI NIH HHS P30 CA016086NCI NIH HHS P30 CA091842NCI NIH HHS U24 CA159988NCI NIH HHS U24-CA-159988NCI NIH HHS U24 CA160019NCI NIH HHS U24-CA-160019NCI NIH HHS U24 CA160034NCI NIH HHS U24-CA-160034NCI NIH HHS U24 CA160035NCI NIH HHS U24-CA-160035NCI NIH HHS U24 CA160036NCI NIH HHS U24-CA-160036NCRR NIH HHS UL1 RR024992PHS HHS HHSN261201100106C
6 · The paper itself

Abstract

The NCI Clinical Proteomic Tumor Analysis Consortium (CPTAC) employed a pair of reference xenograft proteomes for initial platform validation and ongoing quality control of its data collection for The Cancer Genome Atlas (TCGA) tumors. These two xenografts, representing basal and luminal-B human breast cancer, were fractionated and analyzed on six mass spectrometers in a total of 46 replicates divided between iTRAQ and label-free technologies, spanning a total of 1095 LC-MS/MS experiments. These data represent a unique opportunity to evaluate the stability of proteomic differentiation by mass spectrometry over many months of time for individual instruments or across instruments running dissimilar workflows. We evaluated iTRAQ reporter ions, label-free spectral counts, and label-free extracted ion chromatograms as strategies for data interpretation (source code is available from http://homepages.uc.edu/~wang2x7/Research.htm ). From these assessments, we found that differential genes from a single replicate were confirmed by other replicates on the same instrument from 61 to 93% of the time. When comparing across different instruments and quantitative technologies, using multiple replicates, differential genes were reproduced by other data sets from 67 to 99% of the time. Projecting gene differences to biological pathways and networks increased the degree of similarity. These overlaps send an encouraging message about the maturity of technologies for proteomic differentiation.

Indexed as

Breast NeoplasmsChromatography, LiquidData Interpretation, StatisticalFemaleGene Expression ProfilingHeterograftsHumansMetabolic Networks and PathwaysObserver VariationProteomeProteomicsQuality ControlReproducibility of ResultsTandem Mass SpectrometryProteomeCPTACDifferential proteomicsiTRAQlabel-freequality controltechnology assessmentxenografts

Identifiers

PMID26653538
PMCPMC4779376

What OpenQuestion holds

Textmetadata
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.