Beyond genomics: Detecting codes and signals in the cellular transcriptome [Plenary speakers]

B. Frey
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Abstract

Summary form only given, as follows. Construction of the discrete genome sequence was the fi rst step in developing a comprehensive understanding of how cellular processes are controlled by bio-molecules and their interactions. That step is now mostly complete and the next step is to determine how DNA subsequences encode instructions for producing RNA transcripts and how continuous abundances of transcripts in cells combine to control activities. This is a much more challenging task than genome assembly, because the encoding of genetic instructions turns out to be far richer than was previously thought, and the detection and analysis of continuous cellular signals is more diffi cult than discrete symbol detection. Only preliminary progress has been made in assembling and analyzing the 'transcriptome' and the fi rst genome-wide data sets enabling the study of transcripts and their interactions have only recently been published. In this talk, I'll describe several open research problems in this area and discuss how they can be approached using representations and algorithms familiar to researchers in the information theory community.
超越基因组学:检测细胞转录组中的代码和信号[全体会议发言]
仅给出摘要形式,如下。离散基因组序列的构建是全面了解生物分子及其相互作用如何控制细胞过程的第一步。这一步现在已经基本完成,下一步是确定DNA子序列如何编码产生RNA转录物的指令,以及细胞中转录物的连续丰度如何结合起来控制活性。这是一项比基因组组装更具挑战性的任务,因为遗传指令的编码比以前想象的要丰富得多,连续细胞信号的检测和分析比离散符号检测更困难。在组装和分析“转录组”方面只取得了初步进展,并且能够研究转录本及其相互作用的第一个全基因组数据集直到最近才发表。在这次演讲中,我将描述这一领域的几个开放研究问题,并讨论如何使用信息理论社区研究人员熟悉的表示和算法来解决这些问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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