John M. Hancock
Accepted Abstracts: J Comput Sci Syst Biol
W ith the explosion in genome and exome sequencing and other High Throughput Sequencing applications attention is increasingly turning to the interpretation of large volumes of sequence data in a wide variety of contexts. Key data types that need to be integrated with sequence and other omics data to make this possible are phenotype and disease data. This is becoming increasingly important with the advent of the International Mouse Phenotyping Consortium and other high- throughput phenotyping projects using model organisms. Phenotype and disease data have historically suffered from a lack of appropriate forms of data representation for computational analysis but this is changing. I will review the current and developing formalisms for representing phenotype and disease and approaches for integrating them with omics data and their use in building heterogeneous data networks.
W ith the explosion in genome and exome sequencing and other High Throughput Sequencing applications attention is increasingly turning to the interpretation of large volumes of sequence data in a wide variety of contexts. Key data types that need to be integrated with sequence and other omics data to make this possible are phenotype and disease data. This is becoming increasingly important with the advent of the International Mouse Phenotyping Consortium and other high- throughput phenotyping projects using model organisms. Phenotype and disease data have historically suffered from a lack of appropriate forms of data representation for computational analysis but this is changing. I will review the current and developing formalisms for representing phenotype and disease and approaches for integrating them with omics data and their use in building heterogeneous data networks.
Journal of Computer Science & Systems Biology received 2279 citations as per Google Scholar report