Evidence map›Paper›PMID 32086521›Full record

ArticleNucleic acids research2020

S3norm: simultaneous normalization of sequencing depth and signal-to-noise ratio in epigenomic data.

Guanjue Xiang, Cheryl A Keller, Belinda Giardine, Lin An, Qunhua Li, Yu Zhang, Ross C Hardison

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed.

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  13. Robust chromatin state annotation.Genome research · 2024
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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

7 authors.

Guanjue XiangThe Bioinformatics and Genomics program, Center for Computational Biology and Bioinformatics, Huck Institutes of the Life Sciences, Wartik Laboratory, The Pennsylvania State University, University Park, PA 16802, USA.
Cheryl A KellerDept. of Biochemistry and Molecular Biology, The Pennsylvania State University, Wartik Laboratory, University Park, PA 16802, USA.
Belinda GiardineDept. of Biochemistry and Molecular Biology, The Pennsylvania State University, Wartik Laboratory, University Park, PA 16802, USA.
Lin AnThe Bioinformatics and Genomics program, Center for Computational Biology and Bioinformatics, Huck Institutes of the Life Sciences, Wartik Laboratory, The Pennsylvania State University, University Park, PA 16802, USA.
Qunhua LiDept. of Statistics, The Pennsylvania State University, Wartik Laboratory, University Park, PA 16802, USA.
Yu ZhangDept. of Statistics, The Pennsylvania State University, Wartik Laboratory, University Park, PA 16802, USA.
Ross C HardisonDept. of Biochemistry and Molecular Biology, The Pennsylvania State University, Wartik Laboratory, University Park, PA 16802, USA.

Funding

Genomic Architecture of LGL LeukemiaR01CA178393 · NCI · UNIVERSITY OF VIRGINIA · PI Thomas P. Loughran, Aakrosh Ratan · 2016 to 2026
$6.5M
VISION: ValIdated Systematic IntegratiON of epigenomic dataR24DK106766 · NIDDK · PENNSYLVANIA STATE UNIVERSITY, THE · PI BLOBEL, GERD A, BODINE, DAVID M. · 2016 to 2020
$6.2M
Statistical methods for improving reproducibility and utility of sequencing dataR01GM109453 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI LI, QUNHUA · 2013 to 2022
$2.3M
A 2D segmentation method for jointly characterizing epigenetic dynamics in multiple cell linesR01GM121613 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI MAHONY, SHAUN AENGUS · 2017 to 2019
$1.0M
NCI NIH HHS R01 CA178393NIDDK NIH HHS R24 DK106766NIGMS NIH HHS R01 GM109453NIGMS NIH HHS R01 GM121613
6 · The paper itself

Abstract

Quantitative comparison of epigenomic data across multiple cell types or experimental conditions is a promising way to understand the biological functions of epigenetic modifications. However, differences in sequencing depth and signal-to-noise ratios in the data from different experiments can hinder our ability to identify real biological variation from raw epigenomic data. Proper normalization is required prior to data analysis to gain meaningful insights. Most existing methods for data normalization standardize signals by rescaling either background regions or peak regions, assuming that the same scale factor is applicable to both background and peak regions. While such methods adjust for differences in sequencing depths, they do not address differences in the signal-to-noise ratios across different experiments. We developed a new data normalization method, called S3norm, that normalizes the sequencing depths and signal-to-noise ratios across different data sets simultaneously by a monotonic nonlinear transformation. We show empirically that the epigenomic data normalized by our method, compared to existing methods, can better capture real biological variation, such as impact on gene expression regulation.

Indexed as

EpigenomicsGene ExpressionHistone CodeRNA-SeqSequence Analysis, DNASoftware

Identifiers

PMID32086521
PMCPMC7192629

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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.