Evidence map›Paper›PMID 33199889›Full record

ArticleNature methods2020

Avant-garde: an automated data-driven DIA data curation tool.

Alvaro Sebastian Vaca Jacome, Ryan Peckner, Nicholas Shulman, Karsten Krug, Katherine C DeRuff, Adam Officer, Karen E Christianson, Brendan MacLean, Michael J MacCoss, Steven A Carr and 1 more

Abstract read
In one paragraph

Article in Nature methods, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Deep representation features from DreamDIACommunications biology · 2021
    Article
  11. Article
  12. Article
  13. An Introduction to Advanced Targeted Acquisition Methods.Molecular & cellular proteomics : MCP · 2021
    Review
  14. Article
  15. 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

11 authors.

Alvaro Sebastian Vaca JacomeBroad Institute of MIT and Harvard, Cambridge, MA, USA. svaca@broadinstitute.org.ORCID http://orcid.org/0000-0001-7664-4660
Ryan PecknerBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Nicholas ShulmanUniversity of Washington Genome Sciences, Seattle, WA, USA.
Karsten KrugBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Katherine C DeRuffBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Adam OfficerBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Karen E ChristiansonBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Brendan MacLeanUniversity of Washington Genome Sciences, Seattle, WA, USA.
Michael J MacCossUniversity of Washington Genome Sciences, Seattle, WA, USA.ORCID http://orcid.org/0000-0003-1853-0256
Steven A CarrBroad Institute of MIT and Harvard, Cambridge, MA, USA.
Jacob D JaffeBroad Institute of MIT and Harvard, Cambridge, MA, USA. jjaffe@inzentx.com.

Funding

There and Back Again: Epigenetic Reinforcement of Cellular Signaling States - OverallU54HG008097 · NHGRI · BROAD INSTITUTE, INC. · PI JAFFE, JACOB DAVID · 2014 to 2019
$9.3M
MICROSCALED PROTEOGENOMICS FOR CANCER CLINICAL TRIALSU01CA214125 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ANURAG, MEENAKSHI, CARR, STEVEN A · 2017 to 2021
$7.0M
Center of Excellence for High Throughput Proteogenomic CharacterizationU24CA210986 · NCI · BROAD INSTITUTE, INC. · PI CARR, STEVEN A, GILLETTE, MICHAEL A · 2016 to 2020
$6.4M
Integrated high throughput proteogenomic data analysis center for CPTACU24CA210979 · NCI · BROAD INSTITUTE, INC. · PI BIRGER, CHET, GETZ, GAD A · 2016 to 2020
$4.4M
NCI NIH HHS U01 CA214125NCI NIH HHS U24 CA210979NCI NIH HHS U24 CA210986NHGRI NIH HHS U54 HG008097
6 · The paper itself

Abstract

Several challenges remain in data-independent acquisition (DIA) data analysis, such as to confidently identify peptides, define integration boundaries, remove interferences, and control false discovery rates. In practice, a visual inspection of the signals is still required, which is impractical with large datasets. We present Avant-garde as a tool to refine DIA (and parallel reaction monitoring) data. Avant-garde uses a novel data-driven scoring strategy: signals are refined by learning from the dataset itself, using all measurements in all samples to achieve the best optimization. We evaluate the performance of Avant-garde using benchmark DIA datasets and show that it can determine the quantitative suitability of a peptide peak, and reach the same levels of selectivity, accuracy, and reproducibility as manual validation. Avant-garde is complementary to existing DIA analysis engines and aims to establish a strong foundation for subsequent analysis of quantitative mass spectrometry data.

Indexed as

Data AnalysisCell LineData CurationData ScienceHEK293 CellsHumansMass SpectrometryPeptidesProteomeProteomicsReproducibility of ResultsSoftwarePeptidesProteome

Identifiers

PMID33199889
PMCPMC7723322

What OpenQuestion holds

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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.