Evidence map›Paper›PMID 36607439›Full record

ArticleBotanical studies2023

MethylC-analyzer: a comprehensive downstream pipeline for the analysis of genome-wide DNA methylation.

Rita Jui-Hsien Lu, Pei-Yu Lin, Ming-Ren Yen, Bing-Heng Wu, Pao-Yang Chen

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Botanical studies, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Rita Jui-Hsien Lu *Institute of Plant and Microbial Biology, Academia Sinica, Taipei, 115, Taiwan.
Pei-Yu Lin *Institute of Plant and Microbial Biology, Academia Sinica, Taipei, 115, Taiwan.
Ming-Ren Yen *Institute of Plant and Microbial Biology, Academia Sinica, Taipei, 115, Taiwan.
Bing-Heng WuInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, 115, Taiwan.
Pao-Yang ChenInstitute of Plant and Microbial Biology, Academia Sinica, Taipei, 115, Taiwan. paoyang@gate.sinica.edu.tw.ORCID http://orcid.org/0000-0002-7402-3075
Institute of Plant and Microbial Biology, Academia Sinica · TWWashington University in St. Louis · US

Funding

Ministry of Science and Technology, Taiwan 108-2313-B-001-013 -MY3Ministry of Science and Technology, Taiwan 109-2313-B-001-009 -MY3Ministry of Science and Technology, Taiwan 111-2311-B-001 -030Ministry of Science and Technology, Taiwan 111 -2927-I-001 -505 -
6 · The paper itself

Abstract

DNA methylation is a crucial epigenetic modification involved in multiple biological processes and diseases. Current approaches for measuring genome-wide DNA methylation via bisulfite sequencing (BS-seq) include whole-genome bisulfite sequencing (WGBS), reduced representation bisulfite sequencing (RRBS), and enzymatic methyl-seq (EM-seq). The computational analysis tools available for BS-seq data include customized aligners for mapping bisulfite-converted reads and computational pipelines for downstream data analysis. Current post-alignment methylation tools are specialized for the interpretation of CG methylation, which is known to dominate mammalian genomes, however, non-CG methylation (CHG and CHH, where H refers to A, C, or T) is commonly observed in plants and fungi and is closely associated with gene regulation, transposon silencing, and plant development. Thus, we have developed a MethylC-analyzer to analyze and visualize post-alignment WGBS, RRBS, and EM-seq data focusing on CG. The tool is able to also analyze non-CG sites to enhance deciphering genomes of plants and fungi. By processing aligned data and gene location files, MethylC-analyzer generates a genome-wide view of methylation levels and methylation in user-specified genomic regions. The meta-plot, for example, allows the investigation of DNA methylation within specific genomic elements. Moreover, our tool identifies differentially methylated regions (DMRs) and investigates the enrichment of genomic features associated with variable methylation. MethylC-analyzer functionality is not limited to specific genomes, and we demonstrated its performance on both plant and human BS-seq data. MethylC-analyzer is a Python- and R-based program designed to perform comprehensive downstream analyses of methylation data, providing an intuitive analysis platform for scientists unfamiliar with DNA methylation analysis. It is available as either a standalone version for command-line uses or a graphical user interface (GUI) and is publicly accessible at https://github.com/RitataLU/MethylC-analyzer .

Indexed as

Bisulfite sequencingDifferentially methylated regionsDNA methylationEnzymatic methyl-seqMethylC-analyzerNext-generation sequencingReduced representation bisulfite sequencingWhole-genome bisulfite sequencing

Identifiers

PMID36607439
PMCPMC9823188
OpenAlexW4313648035

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.