Evidence map›Paper›PMID 26163275›Full record

ArticleBMC bioinformatics2015

BSPAT: a fast online tool for DNA methylation co-occurrence pattern analysis based on high-throughput bisulfite sequencing data.

Ke Hu, Angela H Ting, Jing Li

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  17. Profiling genome-wide DNA methylation.Epigenetics & chromatin · 2016
    Review
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 at 2 institutions in 1 country.

Ke HuDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, 44106, Ohio, USA. jingli@cwru.edu.
Angela H TingGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, 44195, Ohio, USA. jingli@cwru.edu.
Jing LiDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, 44106, Ohio, USA. jingli@cwru.edu.
Case Western Reserve University · USCleveland Clinic Lerner College of Medicine · US

Funding

Genetic causes of developmental speech sound disorder in familiesR01DC012380 · NIDCD · CASE WESTERN RESERVE UNIVERSITY · PI IYENGAR, SUDHA K · 2012 to 2016
$3.2M
Characterizing the DNA methylomes of indolent and aggressive prostate cancersR01CA154356 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI TING, ANGELA H · 2011 to 2015
$1.6M
NCI NIH HHS CA154356NCI NIH HHS R01 CA154356NIDCD NIH HHS DC012380NIDCD NIH HHS R01 DC012380
6 · The paper itself

Abstract

backgroundBisulfite sequencing is one of the most widely used technologies in analyzing DNA methylation patterns, which are important in understanding and characterizing the mechanism of DNA methylation and its functions in disease development. Efficient and user-friendly tools are critical in carrying out such analysis on high-throughput bisulfite sequencing data. However, existing tools are either not scalable well, or inadequate in providing visualization and other desirable functionalities.

resultsIn order to handle ultra large sequencing data and to provide additional functions and features, we have developed BSPAT, a fast online tool for bisulfite sequencing pattern analysis. With a user-friendly web interface, BSPAT seamlessly integrates read mapping/quality control/methylation calling with methylation pattern generation and visualization. BSPAT has the following important features: 1) instead of using multiple/pairwise sequence alignment methods, BSPAT adopts an efficient and widely used sequence mapping tool to provide fast alignment of sequence reads; 2) BSPAT summarizes and visualizes DNA methylation co-occurrence patterns at a single nucleotide level, which provide valuable information in understanding the mechanism and regulation of DNA methylation; 3) based on methylation co-occurrence patterns, BSPAT can automatically detect potential allele-specific methylation (ASM) patterns, which can greatly enhance the detection and analysis of ASM patterns; 4) by linking directly with other popular databases and tools, BSPAT allows users to perform integrative analysis of methylation patterns with other genomic features together within regions of interest.

conclusionBy utilizing a real bisulfite sequencing dataset generated from prostate cancer cell lines, we have shown that BSPAT is highly efficient. It has also reported some interesting methylation co-occurrence patterns and a potential allele-specific methylation case. In conclusion, BSPAT is an efficient and convenient tool for high-throughput bisulfite sequencing data analysis that can be broadly used.

Indexed as

DNA MethylationSoftwareBase SequenceCell Line, TumorGenomicsHigh-Throughput Nucleotide SequencingHumansMaleMolecular Sequence DataProstatic NeoplasmsSequence AlignmentSequence Analysis, DNASequence Homology, Nucleic AcidSulfiteshydrogen sulfiteSulfites

Identifiers

PMID26163275
PMCPMC4499179
OpenAlexW1499825413

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.