Development of a fixed module repertoire for the analysis and interpretation of blood transcriptome data.

Development of a fixed module repertoire for the analysis and interpretation of blood transcriptome data.
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DOI:
10.1038/s41467-021-24584-w
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发表时间:
2021-07-19
影响因子:
16.6
通讯作者:
Chaussabel D
Chaussabel D
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Altman MC;Rinchai D;Baldwin N;Toufiq M;Whalen E;Garand M;Syed Ahamed Kabeer B;Alfaki M;Presnell SR;Khaenam P;Ayllón-Benítez A;Mougin F;Thébault P;Chiche L;Jourde-Chiche N;Phillips JT;Klintmalm G;O'Garra A;Berry M;Bloom C;Wilkinson RJ;Graham CM;Lipman M;Lertmemongkolchai G;Bedognetti D;Thiebaut R;Kheradmand F;Mejias A;Ramilo O;Palucka K;Pascual V;Banchereau J;Chaussabel D

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As the capacity for generating large-scale molecular profiling data continues to grow, the ability to extract meaningful biological knowledge from it remains a limitation. Here, we describe the development of a new fixed repertoire of transcriptional modules, BloodGen3, that is designed to serve as a stable reusable framework for the analysis and interpretation of blood transcriptome data. The construction of this repertoire is based on co-clustering patterns observed across sixteen immunological and physiological states encompassing 985 blood transcriptome profiles. Interpretation is supported by customized resources, including module-level analysis workflows, fingerprint grid plot visualizations, interactive web applications and an extensive annotation framework comprising functional profiling reports and reference transcriptional profiles. Taken together, this well-characterized and well-supported transcriptional module repertoire can be employed for the interpretation and benchmarking of blood transcriptome profiles within and across patient cohorts. Blood transcriptome fingerprints for the 16 reference cohorts can be accessed interactively via: https://drinchai.shinyapps.io/BloodGen3Module/. The blood transcriptome of human subjects can be profiled on an almost routine basis in translational research settings. Here the authors show that a fixed and well-characterized repertoire of transcriptional modules can be employed as a reusable framework for the analysis, visualization and interpretation of such data
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