Measuring the reproducibility and quality of Hi-C data
Abstract Background Hi-C is currently the most widely used assay to investigate the 3D organization of the genome and to study its role in gene regulation, DNA replication, and disease. However, Hi-C experiments are costly to perform and involve multiple complex experimental steps; thus, accurate me...
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doaj-c5c3304bc21c457993be8f6384642f012020-11-25T03:29:27ZengBMCGenome Biology1474-760X2019-03-0120111910.1186/s13059-019-1658-7Measuring the reproducibility and quality of Hi-C dataGalip Gürkan Yardımcı0Hakan Ozadam1Michael E. G. Sauria2Oana Ursu3Koon-Kiu Yan4Tao Yang5Abhijit Chakraborty6Arya Kaul7Bryan R. Lajoie8Fan Song9Ye Zhan10Ferhat Ay11Mark Gerstein12Anshul Kundaje13Qunhua Li14James Taylor15Feng Yue16Job Dekker17William S. Noble18Department of Genome Sciences, University of WashingtonProgram in Systems Biology, University of Massachusetts Medical SchoolBiology Department, Johns Hopkins UniversityDepartment of Genetics, Stanford UniversityDepartment of Computational Biology, St. Jude Children’s Research HospitalBioinformatics and Genomics Program, Huck Institutes of the Life Sciences, Penn State UniversityComputational Biology Division, La Jolla Institute for Allergy and ImmunologyComputational Biology Division, La Jolla Institute for Allergy and ImmunologyProgram in Systems Biology, University of Massachusetts Medical SchoolBioinformatics and Genomics Program, Huck Institutes of the Life Sciences, Penn State UniversityUniversity of Massachusetts Medical SchoolComputational Biology Division, La Jolla Institute for Allergy and ImmunologyProgram in Computational Biology and Bioinformatics, Yale UniversityDepartment of Genetics, Stanford UniversityDepartment of Statistics, Penn State UniversityBiology Department, Johns Hopkins UniversityBioinformatics and Genomics Program, Huck Institutes of the Life Sciences, Penn State UniversityProgram in Systems Biology, University of Massachusetts Medical SchoolDepartment of Genome Sciences, University of WashingtonAbstract Background Hi-C is currently the most widely used assay to investigate the 3D organization of the genome and to study its role in gene regulation, DNA replication, and disease. However, Hi-C experiments are costly to perform and involve multiple complex experimental steps; thus, accurate methods for measuring the quality and reproducibility of Hi-C data are essential to determine whether the output should be used further in a study. Results Using real and simulated data, we profile the performance of several recently proposed methods for assessing reproducibility of population Hi-C data, including HiCRep, GenomeDISCO, HiC-Spector, and QuASAR-Rep. By explicitly controlling noise and sparsity through simulations, we demonstrate the deficiencies of performing simple correlation analysis on pairs of matrices, and we show that methods developed specifically for Hi-C data produce better measures of reproducibility. We also show how to use established measures, such as the ratio of intra- to interchromosomal interactions, and novel ones, such as QuASAR-QC, to identify low-quality experiments. Conclusions In this work, we assess reproducibility and quality measures by varying sequencing depth, resolution and noise levels in Hi-C data from 13 cell lines, with two biological replicates each, as well as 176 simulated matrices. Through this extensive validation and benchmarking of Hi-C data, we describe best practices for reproducibility and quality assessment of Hi-C experiments. We make all software publicly available at http://github.com/kundajelab/3DChromatin_ReplicateQC to facilitate adoption in the community.http://link.springer.com/article/10.1186/s13059-019-1658-7 |
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English |
format |
Article |
sources |
DOAJ |
author |
Galip Gürkan Yardımcı Hakan Ozadam Michael E. G. Sauria Oana Ursu Koon-Kiu Yan Tao Yang Abhijit Chakraborty Arya Kaul Bryan R. Lajoie Fan Song Ye Zhan Ferhat Ay Mark Gerstein Anshul Kundaje Qunhua Li James Taylor Feng Yue Job Dekker William S. Noble |
spellingShingle |
Galip Gürkan Yardımcı Hakan Ozadam Michael E. G. Sauria Oana Ursu Koon-Kiu Yan Tao Yang Abhijit Chakraborty Arya Kaul Bryan R. Lajoie Fan Song Ye Zhan Ferhat Ay Mark Gerstein Anshul Kundaje Qunhua Li James Taylor Feng Yue Job Dekker William S. Noble Measuring the reproducibility and quality of Hi-C data Genome Biology |
author_facet |
Galip Gürkan Yardımcı Hakan Ozadam Michael E. G. Sauria Oana Ursu Koon-Kiu Yan Tao Yang Abhijit Chakraborty Arya Kaul Bryan R. Lajoie Fan Song Ye Zhan Ferhat Ay Mark Gerstein Anshul Kundaje Qunhua Li James Taylor Feng Yue Job Dekker William S. Noble |
author_sort |
Galip Gürkan Yardımcı |
title |
Measuring the reproducibility and quality of Hi-C data |
title_short |
Measuring the reproducibility and quality of Hi-C data |
title_full |
Measuring the reproducibility and quality of Hi-C data |
title_fullStr |
Measuring the reproducibility and quality of Hi-C data |
title_full_unstemmed |
Measuring the reproducibility and quality of Hi-C data |
title_sort |
measuring the reproducibility and quality of hi-c data |
publisher |
BMC |
series |
Genome Biology |
issn |
1474-760X |
publishDate |
2019-03-01 |
description |
Abstract Background Hi-C is currently the most widely used assay to investigate the 3D organization of the genome and to study its role in gene regulation, DNA replication, and disease. However, Hi-C experiments are costly to perform and involve multiple complex experimental steps; thus, accurate methods for measuring the quality and reproducibility of Hi-C data are essential to determine whether the output should be used further in a study. Results Using real and simulated data, we profile the performance of several recently proposed methods for assessing reproducibility of population Hi-C data, including HiCRep, GenomeDISCO, HiC-Spector, and QuASAR-Rep. By explicitly controlling noise and sparsity through simulations, we demonstrate the deficiencies of performing simple correlation analysis on pairs of matrices, and we show that methods developed specifically for Hi-C data produce better measures of reproducibility. We also show how to use established measures, such as the ratio of intra- to interchromosomal interactions, and novel ones, such as QuASAR-QC, to identify low-quality experiments. Conclusions In this work, we assess reproducibility and quality measures by varying sequencing depth, resolution and noise levels in Hi-C data from 13 cell lines, with two biological replicates each, as well as 176 simulated matrices. Through this extensive validation and benchmarking of Hi-C data, we describe best practices for reproducibility and quality assessment of Hi-C experiments. We make all software publicly available at http://github.com/kundajelab/3DChromatin_ReplicateQC to facilitate adoption in the community. |
url |
http://link.springer.com/article/10.1186/s13059-019-1658-7 |
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