Evidence map›Paper›PMID 32487025›Full record

ArticleBMC bioinformatics2020

CRISPRpred(SEQ): a sequence-based method for sgRNA on target activity prediction using traditional machine learning.

Ali Haisam Muhammad Rafid, Md Toufikuzzaman, Mohammad Saifur Rahman, M Sohel Rahman

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
–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

20 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  7. Prediction of CRISPR-Cas9 on-target activity based on a hybrid neural network.Computational and structural biotechnology journal · 2025
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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

4 authors.

Ali Haisam Muhammad RafidDepartment of Computer Science and Engineering, Bangladesh University of Engineering and Technology, Dhaka, Bangladesh.
Md ToufikuzzamanDepartment of Computer Science and Engineering, Bangladesh University of Engineering and Technology, Dhaka, Bangladesh.
Mohammad Saifur RahmanDepartment of Computer Science and Engineering, Bangladesh University of Engineering and Technology, Dhaka, Bangladesh.
M Sohel RahmanDepartment of Computer Science and Engineering, Bangladesh University of Engineering and Technology, Dhaka, Bangladesh. msrahman@cse.buet.ac.bd.ORCID http://orcid.org/0000-0001-9419-6478

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe latest works on CRISPR genome editing tools mainly employs deep learning techniques. However, deep learning models lack explainability and they are harder to reproduce. We were motivated to build an accurate genome editing tool using sequence-based features and traditional machine learning that can compete with deep learning models.

resultsIn this paper, we present CRISPRpred(SEQ), a method for sgRNA on-target activity prediction that leverages only traditional machine learning techniques and hand-crafted features extracted from sgRNA sequences. We compare the results of CRISPRpred(SEQ) with that of DeepCRISPR, the current state-of-the-art, which uses a deep learning pipeline. Despite using only traditional machine learning methods, we have been able to beat DeepCRISPR for the three out of four cell lines in the benchmark dataset convincingly (2.174%, 6.905% and 8.119% improvement for the three cell lines).

conclusionCRISPRpred(SEQ) has been able to convincingly beat DeepCRISPR in 3 out of 4 cell lines. We believe that by exploring further, one can design better features only using the sgRNA sequences and can come up with a better method leveraging only traditional machine learning algorithms that can fully beat the deep learning models.

Indexed as

Machine LearningAlgorithmsArea Under CurveBase SequenceCRISPR-Cas SystemsDatabases, GeneticDeep LearningGene EditingHEK293 CellsHumansReproducibility of ResultsRNA, Guide, CRISPR-Cas SystemsROC CurveRNA, Guide, CRISPR-Cas SystemsCas9CRISPRDeep learningMachine learningsgRNA

Identifiers

PMID32487025
PMCPMC7268231

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.