2019
DOI: 10.1142/s0219720019500082
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Fast and memory efficient approach for mapping NGS reads to a reference genome

Abstract: New generation sequencing machines: Illumina and Solexa can generate millions of short reads from a given genome sequence on a single run. Alignment of these reads to a reference genome is a core step in Next-generation sequencing data analysis such as genetic variation and genome re-sequencing etc. Therefore there is a need of a new approach, efficient with respect to memory as well as time to align these enormous reads with the reference genome. Existing techniques such as MAQ, Bowtie, BWA, BWBBLE, Subread, … Show more

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Cited by 22 publications
(10 citation statements)
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“…To identify SNPs and indels, filtered reads were aligned to the Nipponbare reference genome sequence [53] using the Burrows-Wheeler Aligner (v.0.7.16a-r1181) with parameter 'mem -M'; -M is an option used to mark shorter split-alignment hits as secondary alignments [54]. Variant calling was performed using the GATK UnifiedGenotyper (v.3.5; https:// gatk.…”
Section: Ngs Sequencing and Bsa-seq Analysismentioning
confidence: 99%
“…To identify SNPs and indels, filtered reads were aligned to the Nipponbare reference genome sequence [53] using the Burrows-Wheeler Aligner (v.0.7.16a-r1181) with parameter 'mem -M'; -M is an option used to mark shorter split-alignment hits as secondary alignments [54]. Variant calling was performed using the GATK UnifiedGenotyper (v.3.5; https:// gatk.…”
Section: Ngs Sequencing and Bsa-seq Analysismentioning
confidence: 99%
“…Genome sequencing was performed by Sangon Biotech. Referring to the GATK best practice-recommended design process, BWA was used to compare the effective data of the sample to the reference genome (Kumar et al, 2019). The SAM tool was used to compare the results for format conversion and sorting, and statistical comparison results (Li et al, 2009).…”
Section: Genome Sequencing and Data Analysismentioning
confidence: 99%
“…japonica genome IRGSP-1.0 (downloaded from Ensembl plants database on 26 September 2019) using the BWA ver. 0.7.12-r1039 aligner [45]. Redundant reads were excluded using the Samtools ver.…”
Section: Chromosomal Localization Of Responsible Loci For Awn Developmentmentioning
confidence: 99%