Evidence map›Paper›PMID 36797269›Full record

ArticleScientific reports2023

Deep reinforcement learning-based pairwise DNA sequence alignment method compatible with embedded edge devices.

Aryan Lall, Siddharth Tallur

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Artificial intelligence in bioinformatics: a survey.Briefings in bioinformatics · 2025
    Review
  2. scFocus: Detecting branching probabilities in single-cell data with SAC.Computational and structural biotechnology journal · 2025
    Article
  3. 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

2 authors.

Aryan LallDepartment of Electrical Engineering (EE), IIT Bombay, Mumbai, 400076, India. aryanlall53@gmail.com.
Siddharth TallurDepartment of Electrical Engineering (EE), IIT Bombay, Mumbai, 400076, India. stallur@ee.iitb.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sequence alignment is an essential component of bioinformatics, for identifying regions of similarity that may indicate functional, structural, or evolutionary relationships between the sequences. Genome-based diagnostics relying on DNA sequencing have benefited hugely from the boom in computing power in recent decades, particularly due to cloud-computing and the rise of graphics processing units (GPUs) and other advanced computing platforms for running advanced algorithms. Translating the success of such breakthroughs in diagnostics to affordable solutions for low-cost healthcare requires development of algorithms that can operate on the edge instead of in the cloud, using low-cost and low-power electronic systems such as microcontrollers and field programmable gate arrays (FPGAs). In this work, we present EdgeAlign, a deep reinforcement learning based method for performing pairwise DNA sequence alignment on stand-alone edge devices. EdgeAlign uses deep reinforcement learning to train a deep Q-network (DQN) agent for performing sequence alignment on fixed length sub-sequences, using a sliding window that is scanned over the length of the entire sequence. The hardware resource-consumption for implementing this scheme is thus independent of the lengths of the sequences to be aligned, and is further optimized using a novel AutoML based method for neural network model size reduction. Unlike other algorithms for sequence alignment reported in literature, the model demonstrated in this work is highly compact and deployed on two edge devices (NVIDIA Jetson Nano Developer Kit and Digilent Arty A7-100T, containing Xilinx XC7A35T Artix-7 FPGA) for demonstration of alignment for sequences from the publicly available Influenza sequences at the National Center for Biotechnology Information (NCBI) Virus Data Hub.

Indexed as

AlgorithmsNeural Networks, ComputerComputersDNASequence AlignmentDNA

Identifiers

PMID36797269
PMCPMC9935504

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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.