Evidence map›Paper›PMID 29621971›Full record

ArticleBMC bioinformatics2018

Linear MALDI-ToF simultaneous spectrum deconvolution and baseline removal.

Vincent Picaud, Jean-Francois Giovannelli, Caroline Truntzer, Jean-Philippe Charrier, Audrey Giremus, Pierre Grangeat, Catherine Mercier

Abstract read
In one paragraph

Article in BMC bioinformatics, 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
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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

7 authors.

Vincent PicaudUniversity of Bordeaux, IMS, UMR 5218, Talence, 33400, France. vincent.picaud@cea.fr.ORCID 0000-0002-0108-8433
Jean-Francois GiovannelliUniversity of Bordeaux, IMS, UMR 5218, Talence, 33400, France.
Caroline TruntzerCLIPP, Pôle de Recherche Université de Bourgogne, Dijon, 21000, France.
Jean-Philippe CharrierTechnology Research Department, Innovation Unit, Marcy l'Étoile, bioMérieux SA, Marcy l'Étoile, 69280, France.
Audrey GiremusUniversity of Bordeaux, IMS, UMR 5218, Talence, 33400, France.
Pierre GrangeatUniversité Grenoble Alpes, Grenoble, 38000, France.
Catherine MercierService de Biostatistique, Hospices Civils de Lyon, Lyon, 69000, France.

Funding

BHI-PRO project, ANR ANR 2010 BLAN 0313
6 · The paper itself

Abstract

backgroundThanks to a reasonable cost and simple sample preparation procedure, linear MALDI-ToF spectrometry is a growing technology for clinical microbiology. With appropriate spectrum databases, this technology can be used for early identification of pathogens in body fluids. However, due to the low resolution of linear MALDI-ToF instruments, robust and accurate peak picking remains a challenging task. In this context we propose a new peak extraction algorithm from raw spectrum. With this method the spectrum baseline and spectrum peaks are processed jointly. The approach relies on an additive model constituted by a smooth baseline part plus a sparse peak list convolved with a known peak shape. The model is then fitted under a Gaussian noise model. The proposed method is well suited to process low resolution spectra with important baseline and unresolved peaks.

resultsWe developed a new peak deconvolution procedure. The paper describes the method derivation and discusses some of its interpretations. The algorithm is then described in a pseudo-code form where the required optimization procedure is detailed. For synthetic data the method is compared to a more conventional approach. The new method reduces artifacts caused by the usual two-steps procedure, baseline removal then peak extraction. Finally some results on real linear MALDI-ToF spectra are provided.

conclusionsWe introduced a new method for peak picking, where peak deconvolution and baseline computation are performed jointly. On simulated data we showed that this global approach performs better than a classical one where baseline and peaks are processed sequentially. A dedicated experiment has been conducted on real spectra. In this study a collection of spectra of spiked proteins were acquired and then analyzed. Better performances of the proposed method, in term of accuracy and reproductibility, have been observed and validated by an extended statistical analysis.

Indexed as

AlgorithmsArtifactsSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationBaselineDeconvolutionMass spectrometryPeak picking

Identifiers

PMID29621971
PMCPMC5887234

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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.