Evidence map›Paper›PMID 31416440›Full record

ArticleBMC bioinformatics2019

FQStat: a parallel architecture for very high-speed assessment of sequencing quality metrics.

Sree K Chanumolu, Mustafa Albahrani, Hasan H Otu

Abstract read
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Genomic epidemiology ofJournal of clinical microbiology · 2026
    Observational
  2. Review
  3. The genesApplied and environmental microbiology · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Sree K ChanumoluDepartment of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE, 68588, USA.
Mustafa AlbahraniDepartment of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE, 68588, USA.
Hasan H OtuDepartment of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE, 68588, USA. hotu2@unl.edu.ORCID http://orcid.org/0000-0002-9253-8152

Funding

Identification and characterization of interaction atlases in humanR21LM012759 · NLM · UNIVERSITY OF NEBRASKA LINCOLN · PI OTU, HASAN · 2018 to 2019
$399k
NIH HHS R21LM012759NLM NIH HHS R21 LM012759
6 · The paper itself

Abstract

backgroundHigh throughput DNA/RNA sequencing has revolutionized biological and clinical research. Sequencing is widely used, and generates very large amounts of data, mainly due to reduced cost and advanced technologies. Quickly assessing the quality of giga-to-tera base levels of sequencing data has become a routine but important task. Identification and elimination of low-quality sequence data is crucial for reliability of downstream analysis results. There is a need for a high-speed tool that uses optimized parallel programming for batch processing and simply gauges the quality of sequencing data from multiple datasets independent of any other processing steps.

resultsFQStat is a stand-alone, platform-independent software tool that assesses the quality of FASTQ files using parallel programming. Based on the machine architecture and input data, FQStat automatically determines the number of cores and the amount of memory to be allocated per file for optimum performance. Our results indicate that in a core-limited case, core assignment overhead exceeds the benefit of additional cores. In a core-unlimited case, there is a saturation point reached in performance by increasingly assigning additional cores per file. We also show that memory allocation per file has a lower priority in performance when compared to the allocation of cores. FQStat's output is summarized in HTML web page, tab-delimited text file, and high-resolution image formats. FQStat calculates and plots read count, read length, quality score, and high-quality base statistics. FQStat identifies and marks low-quality sequencing data to suggest removal from downstream analysis. We applied FQStat on real sequencing data to optimize performance and to demonstrate its capabilities. We also compared FQStat's performance to similar quality control (QC) tools that utilize parallel programming and attained improvements in run time.

conclusionsFQStat is a user-friendly tool with a graphical interface that employs a parallel programming architecture and automatically optimizes its performance to generate quality control statistics for sequencing data. Unlike existing tools, these statistics are calculated for multiple datasets and separately at the "lane," "sample," and "experiment" level to identify subsets of the samples with low quality, thereby preventing the loss of complete samples when reliable data can still be obtained.

Indexed as

SoftwareDatabases, Nucleic AcidHigh-Throughput Nucleotide SequencingHumansQuality ControlSequence Analysis, DNASequence Analysis, RNATime FactorsFASTQParallel programmingSequence quality

Identifiers

PMID31416440
PMCPMC6694608

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.