2022
DOI: 10.1093/bioinformatics/btac137
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BWA-MEME: BWA-MEM emulated with a machine learning approach

Abstract: Motivation The growing use of next-generation sequencing and enlarged sequencing throughput require efficient short-read alignment, where seeding is one of the major performance bottlenecks. The key challenge in the seeding phase is searching for exact matches of substrings of short reads in the reference DNA sequence. Existing algorithms, however, present limitations in performance due to their frequent memory accesses. Results … Show more

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Cited by 105 publications
(60 citation statements)
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“…Raw sequencing data were quality-checked and cleaned using fastp 46 (version 0.21.0). All cleaned reads were aligned to the MSU v7.0 reference genome seudomolecules/version_7.0/all.dir/) using BWA 47 (mem algorithm, version 0.7.17) with default parameters. SAMtools 48 (version 1.5, option -markdup) was used for complete removal of any PCR duplicates.…”
Section: G4dp-seq Protocol In Vitromentioning
confidence: 99%
“…Raw sequencing data were quality-checked and cleaned using fastp 46 (version 0.21.0). All cleaned reads were aligned to the MSU v7.0 reference genome seudomolecules/version_7.0/all.dir/) using BWA 47 (mem algorithm, version 0.7.17) with default parameters. SAMtools 48 (version 1.5, option -markdup) was used for complete removal of any PCR duplicates.…”
Section: G4dp-seq Protocol In Vitromentioning
confidence: 99%
“…For the Circle-Seq data, eccDNAs identification was performed using Circle-Map (https://github.com/iprada/Circle-Map), the algorithm accurately detects circular DNA formed from mappable and non-mappable regions of a genome (Prada-Luengo et al 2019). First, we used BWA (Jung and Han 2022) to align the reads to the human genome hg38 downloaded from GENCODE (https://www.gencodegenes.org/) (Harrow J et al 2012). Then SAMtools (Li et al 2009) was used to index the results in SAM/BAM format to compare the results.…”
Section: Methodsmentioning
confidence: 99%
“…RNA-Seq reads were aligned to the repeat-masked genome assembly using HISAT2 v2.2.1 [ 42 ]. The ONT long reads and genomic Illumina short reads were mapped to the unmasked genome assembly with minimap2 v2.21-r1071 [ 43 ] and BWA-MEM2 v2.2.1 [ 44 ], respectively ( Table S1 ).…”
Section: Methodsmentioning
confidence: 99%