Using ICLite for deconvolution of bulk transcriptional data from mixed cell populations.
Using ICLite for deconvolution of bulk transcriptional data from mixed cell populations.
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DOI:
10.1016/j.xpro.2021.100847
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发表时间:
2021-12-17
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影响因子:
--
通讯作者:
Ray A
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文献类型:
--
作者:
Camiolo MJ;Wenzel SE;Ray A
Bulk expression data from heterogeneous cell populations pose a challenge for investigators, as differences in cell numbers and transcriptional programs may complicate analysis. To improve the performance of bulk RNA sequencing on mixed populations, we created Immune Cell Linkage through Exploratory Matrices (ICLite). The ICLite package for R constructs modules of correlated genes and identifies their relationship to specific lineages in mixed cell populations. This protocol details formatting, optimization of run parameters, and interpretation of results following implementation of ICLite. For complete details on the use and execution of this protocol, please refer to. ICLite identifies gene modules in bulk transcriptional data from mixed cell populations Protocol details how to run and interpret the results of ICLite Discussion of parameter tuning, data formatting, and solution evaluation Details for post-run exploration including gene ontology and semantic similarity Bulk expression data from heterogeneous cell populations pose a challenge for investigators, as differences in cell numbers and transcriptional programs may complicate analysis. To improve the performance of bulk RNA sequencing on mixed populations, we created Immune Cell Linkage through Exploratory Matrices (ICLite). The ICLite package for R constructs modules of correlated genes and identifies their relationship to specific lineages in mixed cell populations. This protocol details formatting, optimization of run parameters, and interpretation of results following implementation of ICLite.
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