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ddClone: joint statistical inference of clonal populations from single cell and bulk tumour sequencing data Salehi, Sohrab; Steif, Adi; Roth, Andrew J. L.; Aparicio, Samuel, 1963-; Bouchard-Côté, Alexandre; Shah, Sohrab P.
Abstract
Next-generation sequencing (NGS) of bulk tumour tissue can identify constituent cell populations in cancers and measure their abundance. This requires computational deconvolution of allelic counts from somatic mutations, which may be incapable of fully resolving the underlying population structure. Single cell sequencing (SCS) is a more direct method, although its replacement of NGS is impeded by technical noise and sampling limitations. We propose ddClone, which analytically integrates NGS and SCS data, leveraging their complementary attributes through joint statistical inference. We show on real and simulated datasets that ddClone produces more accurate results than can be achieved by either method alone.
Item Metadata
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ddClone: joint statistical inference of clonal populations from single cell and bulk tumour sequencing data
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Publisher |
BioMed Central
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Date Issued |
2017-03-01
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Description |
Next-generation sequencing (NGS) of bulk tumour tissue can identify constituent cell populations in cancers and measure their abundance. This requires computational deconvolution of allelic counts from somatic mutations, which may be incapable of fully resolving the underlying population structure. Single cell sequencing (SCS) is a more direct method, although its replacement of NGS is impeded by technical noise and sampling limitations. We propose ddClone, which analytically integrates NGS and SCS data, leveraging their complementary attributes through joint statistical inference. We show on real and simulated datasets that ddClone produces more accurate results than can be achieved by either method alone.
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Language |
eng
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Date Available |
2017-12-14
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution 4.0 International (CC BY 4.0)
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DOI |
10.14288/1.0362034
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URI | |
Affiliation | |
Citation |
Genome Biology. 2017 Mar 01;18(1):44
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Publisher DOI |
10.1186/s13059-017-1169-3
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty
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Copyright Holder |
The Author(s)
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DSpace
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Item Citations and Data
Rights
Attribution 4.0 International (CC BY 4.0)