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Several functions are provided for dose-response (or concentration-response) characterization from omics data. 'DRomics' is especially dedicated to omics data obtained using a typical dose-response design, favoring a great number of tested doses (or concentrations) rather than a great number of replicates (no need of replicates). 'DRomics' provides functions 1) to check, normalize and or transform data, 2) to select monotonic or biphasic significantly responding items (e.g. probes, metabolites), 3) to choose the best-fit model among a predefined family of monotonic and biphasic models to describe each selected item, 4) to derive a benchmark dose or concentration and a typology of response from each fitted curve. In the available version data are supposed to be single-channel microarray data in log2, RNAseq data in raw counts, or already pretreated continuous omics data (such as metabolomic data) in log scale. In order to link responses across biological levels based on a common method, 'DRomics' also handles apical data as long as they are continuous and follow a normal distribution for each dose or concentration, with a common standard error. For further details see Delignette-Muller et al (2023) <doi:10.24072/pcjournal.325> and Larras et al (2018) <doi:10.1021/acs.est.8b04752>.
Property / description: Several functions are provided for dose-response (or concentration-response) characterization from omics data. 'DRomics' is especially dedicated to omics data obtained using a typical dose-response design, favoring a great number of tested doses (or concentrations) rather than a great number of replicates (no need of replicates). 'DRomics' provides functions 1) to check, normalize and or transform data, 2) to select monotonic or biphasic significantly responding items (e.g. probes, metabolites), 3) to choose the best-fit model among a predefined family of monotonic and biphasic models to describe each selected item, 4) to derive a benchmark dose or concentration and a typology of response from each fitted curve. In the available version data are supposed to be single-channel microarray data in log2, RNAseq data in raw counts, or already pretreated continuous omics data (such as metabolomic data) in log scale. In order to link responses across biological levels based on a common method, 'DRomics' also handles apical data as long as they are continuous and follow a normal distribution for each dose or concentration, with a common standard error. For further details see Delignette-Muller et al (2023) <doi:10.24072/pcjournal.325> and Larras et al (2018) <doi:10.1021/acs.est.8b04752>. / rank
 
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Property / author: Marie-Laure Laure Delignette-Muller / rank
 
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Property / author
 
Property / author: Elise Billoir / rank
 
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Property / author
 
Property / author: Aurélie Siberchicot / rank
 
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Property / copyright license: GNU General Public License, version 2.0 / rank
 
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Property / copyright license: GNU General Public License, version 3.0 / rank
 
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Property / copyright license: GNU General Public License, version 3.0 / qualifier
 
edition/version: expanded from: GPL (≥ 2) (English)
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Property / cites work: DRomics, a workflow to exploit dose-response omics data in ecotoxicology / rank
 
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Property / cites work
 
Property / cites work: DRomics: A Turnkey Tool to Support the Use of the Dose–Response Framework for Omics Data in Ecological Risk Assessment / rank
 
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Latest revision as of 19:56, 12 March 2024

Dose Response for Omics
Language Label Description Also known as
English
DRomics
Dose Response for Omics

    Statements

    0 references
    2.5-0
    24 January 2023
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    1.0-2
    16 January 2019
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    2.0-1
    16 September 2019
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    2.1-2
    22 September 2020
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    2.1-3
    23 September 2020
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    2.2-0
    9 February 2021
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    2.3-0
    4 October 2021
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    2.4-0
    6 January 2022
    0 references
    2.5-2
    31 January 2024
    0 references
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    0 references
    31 January 2024
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    Several functions are provided for dose-response (or concentration-response) characterization from omics data. 'DRomics' is especially dedicated to omics data obtained using a typical dose-response design, favoring a great number of tested doses (or concentrations) rather than a great number of replicates (no need of replicates). 'DRomics' provides functions 1) to check, normalize and or transform data, 2) to select monotonic or biphasic significantly responding items (e.g. probes, metabolites), 3) to choose the best-fit model among a predefined family of monotonic and biphasic models to describe each selected item, 4) to derive a benchmark dose or concentration and a typology of response from each fitted curve. In the available version data are supposed to be single-channel microarray data in log2, RNAseq data in raw counts, or already pretreated continuous omics data (such as metabolomic data) in log scale. In order to link responses across biological levels based on a common method, 'DRomics' also handles apical data as long as they are continuous and follow a normal distribution for each dose or concentration, with a common standard error. For further details see Delignette-Muller et al (2023) <doi:10.24072/pcjournal.325> and Larras et al (2018) <doi:10.1021/acs.est.8b04752>.
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