日本毒性学会学術年会
第43回日本毒性学会学術年会
セッションID: S14-4
会議情報

シンポジウム14 適応拡大する毒性オミクス
クラスタリングと比較ゲノム解析による遺伝子ネットワークメカニズムの推定
*ポリュリャーフ ナターリア北野 宏明
著者情報
会議録・要旨集 フリー

詳細
抄録
‘Percellome’ database is a unique source of toxicity response data for more than 100 chemicals obtained on various organs of mice (Kanno group, NIHS). Originally developed “per cell” readout in mRNA copy method with a high precision in measuring gene expression permits to include each molecule to the network analysis, treating cell as an Open System.

We have developed two software tools: AGCT (A Geometric Clustering Tool) and SHOE (Sequence HOmology in higher Eukaryotes) promoter analyzer suitable for ‘Percellome’ data. AGCT analyses large-scale (40,000n probes) time-series data with spectral clustering manifold that represents and visualize complex data in low dimension.

Subsequently low dimension manifold is clustered with novel techniques such as Bregman K-means, Affinity Propagation (AP), Non-Negative Matrix Factorization (NNMF), Expecation Maximization and others to reach the finite number of clusters with similar expression profile. Those clusters are hereafter analyzed on SHOE, which aims to predict transcription factors network basing on phylogenetic footprinting of three genomes: human, mouse and rat.

Since AGCT and SHOE are connected to Garuda platform (Systems Biology Institute), their outputs can be automatically passed to other tools on Garuda platform for further analysis or visualization.
著者関連情報
© 2016 日本毒性学会
前の記事 次の記事
feedback
Top