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The dynseq genome browser track enables visualization of context-specific, dynamic DNA sequence features at single nucleotide resolution

View ORCID ProfileSurag Nair, Arjun Barrett, View ORCID ProfileDaofeng Li, View ORCID ProfileBrian J Raney, View ORCID ProfileBrian T Lee, Peter Kerpedjiev, View ORCID ProfileVivekanandan Ramalingam, Anusri Pampari, View ORCID ProfileFritz Lekschas, View ORCID ProfileTing Wang, View ORCID ProfileMaximilian Haeussler, View ORCID ProfileAnshul Kundaje
doi: https://doi.org/10.1101/2022.05.26.493621
Surag Nair
1Department of Computer Science, Stanford University
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Arjun Barrett
2The Harker School, San Jose, CA
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Daofeng Li
3Department of Genetics, Washington University in St. Louis School of Medicine
4Edison Family Center for Genome Sciences and Systems Biology, Washington University in St. Louis School of Medicine
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Brian J Raney
5Genomics Institute, University of California Santa Cruz, Santa Cruz, CA
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Brian T Lee
5Genomics Institute, University of California Santa Cruz, Santa Cruz, CA
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Peter Kerpedjiev
6Reservoir Genomics LLC, Oakland, CA
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Vivekanandan Ramalingam
7Department of Genetics, Stanford University
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Anusri Pampari
1Department of Computer Science, Stanford University
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Fritz Lekschas
8Ozette Technologies, Seattle, WA, USA
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Ting Wang
3Department of Genetics, Washington University in St. Louis School of Medicine
4Edison Family Center for Genome Sciences and Systems Biology, Washington University in St. Louis School of Medicine
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Maximilian Haeussler
5Genomics Institute, University of California Santa Cruz, Santa Cruz, CA
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Anshul Kundaje
1Department of Computer Science, Stanford University
7Department of Genetics, Stanford University
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  • For correspondence: akundaje@stanford.edu
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Abstract

We introduce the dynseq genome browser track, which displays DNA nucleotide characters scaled by user-specified, base-resolution scores provided in the BigWig file format. The dynseq track enables visualization of context-specific, informative genomic sequence features. We demonstrate its utility in three popular genome browsers for interpreting cis-regulatory sequence syntax and regulatory variant interpretation by visualizing nucleotide importance scores derived from machine learning models of regulatory DNA trained on protein-DNA binding and chromatin accessibility experiments.

Competing Interest Statement

A.K. is scientific co-founder of Ravel Biotechnology Inc., is on the scientific advisory board of PatchBio Inc., SerImmune Inc., AINovo Inc., TensorBio Inc. and OpenTargets, is a consultant with Illumina Inc. and owns shares in DeepGenomics Inc., Immuni Inc. and Freenome Inc.

Footnotes

  • 1 typo: SP1 ->; SPI1 Supp Table 1 -> Supplementary Table 1 Minor change to first line of last paragraph: "Genome browsers are an indispensable tool for the analysis of epigenetic data" -> "Genome browsers are an indispensable tool for the analysis of genomic and biochemical profiling experiments"

  • https://doi.org/10.5281/zenodo.6582100

  • https://github.com/kundajelab/dynseq-paper

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted May 31, 2022.
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The dynseq genome browser track enables visualization of context-specific, dynamic DNA sequence features at single nucleotide resolution
Surag Nair, Arjun Barrett, Daofeng Li, Brian J Raney, Brian T Lee, Peter Kerpedjiev, Vivekanandan Ramalingam, Anusri Pampari, Fritz Lekschas, Ting Wang, Maximilian Haeussler, Anshul Kundaje
bioRxiv 2022.05.26.493621; doi: https://doi.org/10.1101/2022.05.26.493621
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The dynseq genome browser track enables visualization of context-specific, dynamic DNA sequence features at single nucleotide resolution
Surag Nair, Arjun Barrett, Daofeng Li, Brian J Raney, Brian T Lee, Peter Kerpedjiev, Vivekanandan Ramalingam, Anusri Pampari, Fritz Lekschas, Ting Wang, Maximilian Haeussler, Anshul Kundaje
bioRxiv 2022.05.26.493621; doi: https://doi.org/10.1101/2022.05.26.493621

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