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• W2495349733 startingPage "475" @default.
• W2495349733 abstract "The postgenomic era is presenting new challenges for bioinformatics. High-through- put genome sequencing and assembly techniques, together with new information resources, such as structural proteomics, transcriptome data from microarray analyses, or light microscopy images of living cells, have led to a rapid increase in the amount of data available, ranging from complete genome sequences to cellular, structure, phenotype, and other types of biologically relevant information. Thus, genomic and proteomic research has transformed molecular biology from a “ data poor” to a “ data rich” science. The question now is whether or not we can make sense of all these data using bioinformatics approaches in such areas as genome annotation, comparative genomics, and gene expression analysis. In the face of this ever-increasing volume of complex and constantly evolving data, the integration of experimental data with bioinformatic comparative and predictive analyses will be crucial to the complete description of protein function, not only at the molecular level but also at the higher levels of the pathways, macro-molecular complexes, cells, or organs a protein belongs to." @default.
• W2495349733 created "2016-08-23" @default.
• W2495349733 creator A5025255544 @default.
• W2495349733 creator A5039921905 @default.
• W2495349733 date "2005-01-01" @default.
• W2495349733 modified "2023-09-23" @default.
• W2495349733 title "New Challenges and Strategies for Multiple Sequence Alignment in the Proteomics Era" @default.
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