2010
DOI: 10.1186/1756-0500-3-257
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A direct comparison of the KB™ Basecaller and phred for identifying the bases from DNA sequencing using chain termination chemistry

Abstract: BackgroundRelatively recently, the software KB™ Basecaller has replaced phred for identifying the bases from raw sequence data in DNA sequencing employing dideoxy chemistry. We have measured quantitatively the consequences of that change.ResultsThe high quality sequence segment of reads derived from the KB™ Basecaller were, on average, 30-to-50 bases longer than reads derived from phred. However, microbe identification appeared to have been unaffected by the change in software.ConclusionsWe have demonstrated a… Show more

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Cited by 10 publications
(6 citation statements)
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“…Individual sequence reads were trimmed, assembled into contigs, and the contigs hand edited as described previously [3], except that the ABI BaseCaller software was employed to identify the bases instead of phred [5].…”
Section: Methodsmentioning
confidence: 99%
“…Individual sequence reads were trimmed, assembled into contigs, and the contigs hand edited as described previously [3], except that the ABI BaseCaller software was employed to identify the bases instead of phred [5].…”
Section: Methodsmentioning
confidence: 99%
“…Individual sequence reads were trimmed for quality and vector sequences, assembled into contigs, and the contigs were hand edited as described 7,8 except that the ABI BaseCaller software was used to identify bases instead of phred. 9 The software Bellerophon, 10 as part of the Greengenes package, 11 was used to identify and remove chimerasPlease provide supplier details for ABI Base-Caller, phred, Quantitative Insights into Microbial Ecology, and Bellerophon.. To minimize variation in these procedures, 1 scientist (MF) conducted all sequencing and processing of the sequence reads.…”
Section: Chain-terminator (Sanger) Sequencing Of the 16s Ribosomal Rna Genementioning
confidence: 99%
“…These trimmed sequences were considered as high-quality (HQ) sequences (92.3% of raw reads). Only nucleotides with Phred “high quality bases” were considered (HQ Phred score >20) [48]. A total of 1,446 mitochondrial transcriptome sequences were identified, matching 93% of the mitochondrial genome reference with a coverage (mean depth per reference base) of 24.51.…”
Section: Resultsmentioning
confidence: 99%