Evidence map›Paper›PMID 31775621›Full record

ArticleBMC bioinformatics2019

A general-purpose signal processing algorithm for biological profiles using only first-order derivative information.

Yuanjie Liu, Jianhan Lin

Abstract readEvaluation Study
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

2 authors.

Yuanjie LiuCollege of Information and Electrical Engineering, China Agricultural University, Haidian, Beijing, 100083, People's Republic of China. yjliu@cau.edu.cn.ORCID http://orcid.org/0000-0002-3041-893X
Jianhan LinCollege of Information and Electrical Engineering, China Agricultural University, Haidian, Beijing, 100083, People's Republic of China.

Funding

Fundamental Research Funds for the Central Universities 2019TC045Young Scientists Fund 61807032
6 · The paper itself

Abstract

backgroundAutomatic signal-feature extraction algorithms are crucial for profile processing in bioinformatics. Both baseline drift and noise seriously affect the position and peak area of signals. An efficient algorithm named the derivative passing accumulation (DPA) method for simultaneous baseline correction and signal extraction is presented in this article. It is an efficient method using only the first-order derivatives which are obtained through taking the simple differences.

resultsWe developed a new signal feature extracting procedure. The vector representing the discrete first-order derivative was divided into negative and positive parts and then accumulated to build a signal descriptor. The signals and background fluctuations are easily separated according to this descriptor via thresholding. In addition, the signal peaks are simultaneously located by checking the corresponding intervals in the descriptor. Therefore, the eternal issues of parsing the 1-dimensional output of detectors in biological instruments are solved together. Thereby, the baseline is corrected, and the signal peaks are extracted.

conclusionsWe have introduced a new method for signal peak picking, where baseline computation and peak identification are performed jointly. The testing results of both authentic and artificially synthesized data illustrate that the new method is powerful, and it could be a better choice for practical processing.

Indexed as

AlgorithmsSignal Processing, Computer-AssistedComputational BiologyHumansBaseline correctionFirst derivativePassing accumulationSignal extraction

Identifiers

PMID31775621
PMCPMC6882060

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Registered trials

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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.