Discovering differential genome sequence activity with interpretable and efficient deep learning.
Discovering sequence features that differentially direct cells to alternate fates is key to understanding both cellular development and the consequences of disease related mutations. We introduce Expected Pattern Effect and Differential Expected Pattern Effect, two black-box methods that can interpr...
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Public Library of Science (PLoS)
2021
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oai:doaj.org-article:f68a75bb216e4deea942b65eba7350a72021-12-02T19:58:07ZDiscovering differential genome sequence activity with interpretable and efficient deep learning.1553-734X1553-735810.1371/journal.pcbi.1009282https://doaj.org/article/f68a75bb216e4deea942b65eba7350a72021-08-01T00:00:00Zhttps://doi.org/10.1371/journal.pcbi.1009282https://doaj.org/toc/1553-734Xhttps://doaj.org/toc/1553-7358Discovering sequence features that differentially direct cells to alternate fates is key to understanding both cellular development and the consequences of disease related mutations. We introduce Expected Pattern Effect and Differential Expected Pattern Effect, two black-box methods that can interpret genome regulatory sequences for cell type-specific or condition specific patterns. We show that these methods identify relevant transcription factor motifs and spacings that are predictive of cell state-specific chromatin accessibility. Finally, we integrate these methods into framework that is readily accessible to non-experts and available for download as a binary or installed via PyPI or bioconda at https://cgs.csail.mit.edu/deepaccess-package/.Jennifer HammelmanDavid K GiffordPublic Library of Science (PLoS)articleBiology (General)QH301-705.5ENPLoS Computational Biology, Vol 17, Iss 8, p e1009282 (2021) |
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Biology (General) QH301-705.5 |
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Biology (General) QH301-705.5 Jennifer Hammelman David K Gifford Discovering differential genome sequence activity with interpretable and efficient deep learning. |
description |
Discovering sequence features that differentially direct cells to alternate fates is key to understanding both cellular development and the consequences of disease related mutations. We introduce Expected Pattern Effect and Differential Expected Pattern Effect, two black-box methods that can interpret genome regulatory sequences for cell type-specific or condition specific patterns. We show that these methods identify relevant transcription factor motifs and spacings that are predictive of cell state-specific chromatin accessibility. Finally, we integrate these methods into framework that is readily accessible to non-experts and available for download as a binary or installed via PyPI or bioconda at https://cgs.csail.mit.edu/deepaccess-package/. |
format |
article |
author |
Jennifer Hammelman David K Gifford |
author_facet |
Jennifer Hammelman David K Gifford |
author_sort |
Jennifer Hammelman |
title |
Discovering differential genome sequence activity with interpretable and efficient deep learning. |
title_short |
Discovering differential genome sequence activity with interpretable and efficient deep learning. |
title_full |
Discovering differential genome sequence activity with interpretable and efficient deep learning. |
title_fullStr |
Discovering differential genome sequence activity with interpretable and efficient deep learning. |
title_full_unstemmed |
Discovering differential genome sequence activity with interpretable and efficient deep learning. |
title_sort |
discovering differential genome sequence activity with interpretable and efficient deep learning. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2021 |
url |
https://doaj.org/article/f68a75bb216e4deea942b65eba7350a7 |
work_keys_str_mv |
AT jenniferhammelman discoveringdifferentialgenomesequenceactivitywithinterpretableandefficientdeeplearning AT davidkgifford discoveringdifferentialgenomesequenceactivitywithinterpretableandefficientdeeplearning |
_version_ |
1718375816119713792 |