ArticleBMC medical genomics2016
Fast comparison of genomic and meta-genomic reads with alignment-free measures based on quality values.
Article in BMC medical genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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.
Who cites it
3 citing papers in PubMed.
- cPlot: Contig-Plotting Visualization for the Analysis of Short-Read Nucleotide Sequence Alignments.International journal of molecular sciences · 2022Article
- Better quality score compression through sequence-based quality smoothing.BMC bioinformatics · 2019Article
- SSAW: A new sequence similarity analysis method based on the stationary discrete wavelet transform.BMC bioinformatics · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSequencing technologies are generating enormous amounts of read data, however assembly of genomes and metagenomes remain among the most challenging tasks. In this paper we study the comparison of genomes and metagenomes only based on read data, using word counts statistics called alignment-free thus not requiring reference genomes or assemblies. Quality scores produced by sequencing platforms are fundamental for various analyses, moreover future-generation sequencing platforms, will produce longer reads but with error rate around 15 %. In this context it will be fundamental to exploit quality values information within the framework of alignment-free measures.
resultsIn this paper we present a family of alignment-free measures, called d (q) -type, that are based on k-mer counts and quality values. These statistics can be used to compare genomes and metagenomes based on their read sets. Results show that the evolutionary relationship of genomes can be reconstructed based on the direct comparison of theirs reads sets.
conclusionThe use of quality values on average improves the classification accuracy, and its contribution increases when the reads are more noisy. Also the comparison of metagenomic microbial communities can be performed efficiently. Similar metagenomes are quickly detected, just by processing their read data, without the need of costly alignments.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.