Evidence map›Paper›PMID 34243709›Full record

ArticleBMC genomics2021

A machine learning approach for accurate and real-time DNA sequence identification.

Yiren Wang, Mashari Alangari, Joshua Hihath, Arindam K Das, M P Anantram

Abstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Overview and Prospects of DNA Sequence Visualization.International journal of molecular sciences · 2025
    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

5 authors.

Yiren WangDepartment of Electrical and Computer Engineering, University of Washington, 98195, Seattle, WA, USA. ethanwyr@uw.edu.
Mashari AlangariElectrical and Computer Engineering Department, University of California Davis, 95616, Davis, CA, USA.
Joshua HihathElectrical and Computer Engineering Department, University of California Davis, 95616, Davis, CA, USA.
Arindam K DasDepartment of Electrical Engineering, Eastern Washington University, 99004, Cheney, WA, USA.
M P AnantramDepartment of Electrical and Computer Engineering, University of Washington, 98195, Seattle, WA, USA. anantmp@uw.edu.

Funding

national science foundation 1807391national science foundation 1807555national science foundation 2036865
6 · The paper itself

Abstract

backgroundThe all-electronic Single Molecule Break Junction (SMBJ) method is an emerging alternative to traditional polymerase chain reaction (PCR) techniques for genetic sequencing and identification. Existing work indicates that the current spectra recorded from SMBJ experimentations contain unique signatures to identify known sequences from a dataset. However, the spectra are typically extremely noisy due to the stochastic and complex interactions between the substrate, sample, environment, and the measuring system, necessitating hundreds or thousands of experimentations to obtain reliable and accurate results.

resultsThis article presents a DNA sequence identification system based on the current spectra of ten short strand sequences, including a pair that differs by a single mismatch. By employing a gradient boosted tree classifier model trained on conductance histograms, we demonstrate that extremely high accuracy, ranging from approximately 96 % for molecules differing by a single mismatch to 99.5 % otherwise, is possible. Further, such accuracy metrics are achievable in near real-time with just twenty or thirty SMBJ measurements instead of hundreds or thousands. We also demonstrate that a tandem classifier architecture, where the first stage is a multiclass classifier and the second stage is a binary classifier, can be employed to boost the single mismatched pair's identification accuracy to 99.5 %.

conclusionsA monolithic classifier, or more generally, a multistage classifier with model specific parameters that depend on experimental current spectra can be used to successfully identify DNA strands.

Indexed as

DNAMachine LearningBase SequenceDNAAll-electrical detectionConductance probability distributionDNA sequence identificationMachine learningSingle Molecule Break Junction

Identifiers

PMID34243709
PMCPMC8268518

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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.