2019
DOI: 10.7454/mst.v23i2.3488
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Use of the “DNAChecker” Algorithm for Improving Bioinformatics Research

Abstract: Basic Local Alignment Sequencing Tool (BLAST) is a bioinformatics tool used for analyzing nucleotide sequences with regards to their similarity. BLAST can be found online on biological databases such as the National Center for Biotechnology Information (NCBI) and other such repositories. The mechanism of BLAST allows the target sequence to be compared with other sequences to find regions of local similarity, and thus, a comparability quotient that determines the resemblance between the sequences is created. Du… Show more

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Cited by 6 publications
(7 citation statements)
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“…BLAST-QC's design for easy integration into high-throughput workflows and pipelines resonates with our use of Biopython, which similarly provides a lightweight and portable solution for BLAST result analysis [24]. Moreover, the 'DNAChecker' algorithm's focus on assessing sequence quality before BLAST analysis complements our methodology, ensuring the effectiveness of the BLAST results by pre-screening the input sequences [25]. This pre-analysis step is crucial, given the open-platform nature of biological databases that often accept sequences with varying quality.…”
Section: Blast Parameter Optimization With Algorithmic Efficiencymentioning
confidence: 92%
“…BLAST-QC's design for easy integration into high-throughput workflows and pipelines resonates with our use of Biopython, which similarly provides a lightweight and portable solution for BLAST result analysis [24]. Moreover, the 'DNAChecker' algorithm's focus on assessing sequence quality before BLAST analysis complements our methodology, ensuring the effectiveness of the BLAST results by pre-screening the input sequences [25]. This pre-analysis step is crucial, given the open-platform nature of biological databases that often accept sequences with varying quality.…”
Section: Blast Parameter Optimization With Algorithmic Efficiencymentioning
confidence: 92%
“…Qualities of the DNA sequences were checked and Phred scores above 30 were considered for downstream analysis. Each strand was manually edited and trimmed using Finch TV to generate consensus sequences [19]. Generated DNA sequences were submitted to the NCBI GenBank and the following accession numbers were assigned.…”
Section: Sequence Analysismentioning
confidence: 99%
“…The Sanger method (1977) was used for DNA sequencing, performed by a sequencing company with the PCR products sent to First Base, Malaysia. The resulting chromatograms were analyzed using bioinformatics software, including Finch TV (Bhat et al 2019), DNA Baser Assembler v5.15.0, Clustal X Version 2.1 (Ferrari and Patrizio 2021), BioEdit Version 7.0.5.3, and MEGA 6.0 (Tamura et al 2013). DNA sequences obtained were used to determine genetic variation, nucleotide and amino acid composition, genetic distance, and relationships within the COX1 gene.…”
Section: Sequencingmentioning
confidence: 99%