Evidence map›Paper›PMID 30221607›Full record

ArticleGenetics research2018

An efficient classification algorithm for NGS data based on text similarity.

Xiangyu Liao, Xingyu Liao, Wufei Zhu, Lu Fang, Xing Chen

Abstract readEvaluation Study
In one paragraph

Article in Genetics research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. UniqueInternational journal of molecular sciences · 2020
    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

5 authors.

Xiangyu LiaoDepartment of Oncology,The First College of Clinical Medical Science,China Three Gorges University,Yichang Central People's Hospital,Yichang,Hubei 443000,P.R. China.
Xingyu LiaoSchool of Information Science and Engineering,Central South University,Changsha,Hunan 410083,P.R. China.
Wufei ZhuDepartment of Endocrinology,The First College of Clinical Medical Science,China Three Gorges University,Yichang Central People's Hospital,Yichang,Hubei 443000,P.R. China.
Lu FangDepartment of Endocrinology,The First College of Clinical Medical Science,China Three Gorges University,Yichang Central People's Hospital,Yichang,Hubei 443000,P.R. China.
Xing ChenDepartment of Endocrinology,The First College of Clinical Medical Science,China Three Gorges University,Yichang Central People's Hospital,Yichang,Hubei 443000,P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the advancement of high-throughput sequencing technologies, the amount of available sequencing data is growing at a pace that has now begun to greatly challenge the data processing and storage capacities of modern computer systems. Removing redundancy from such data by clustering could be crucial for reducing memory, disk space and running time consumption. In addition, it also has good performance on reducing dataset noise in some analysis applications. In this study, we propose a high-performance short sequence classification algorithm (HSC) for next generation sequencing (NGS) data based on efficient hash function and text similarity. First, HSC converts all reads into k-mers, then it forms a unique k-mer set by merging the duplicated and reverse complementary elements. Second, all unique k-mers are stored in a hash table, where the k-mer string is stored in the key field, and the ID of the reads containing the k-mer are stored in the value field. Third, each hash unit is transformed into a short text consisting of reads. Fourth, texts that satisfy the similarity threshold are combined into a long text, the merge operation is executed iteratively until there is no text that satisfies the merge condition. Finally, the long text is transformed into a cluster consisting of reads. We tested HSC using five real datasets. The experimental results showed that HSC cluster 100 million short reads within 2 hours, and it has excellent performance in reducing memory consumption. Compared to existing methods, HSC is much faster than other tools, it can easily handle tens of millions of sequences. In addition, when HSC is used as a preprocessing tool to produce assembly data, the memory and time consumption of the assembler is greatly reduced. It can help the assembler to achieve better assemblies in terms of N50, NA50 and genome fraction.

Indexed as

AlgorithmsHigh-Throughput Nucleotide SequencingData AnalysisDatasets as TopicHumansMycobacterium abscessusRhodobacter sphaeroidesVibrio choleraeclusteringNGS sequences datatext similarity

Identifiers

PMID30221607
PMCPMC6865153

What OpenQuestion holds

Textmetadata
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.