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PANTHER: Making genome-scale phylogenetics accessible to all

期刊

PROTEIN SCIENCE
卷 31, 期 1, 页码 8-22

出版社

WILEY
DOI: 10.1002/pro.4218

关键词

gene ontology; genome analysis; hidden Markov model; molecular evolution; omics data analysis; phylogenetic tree; protein function annotation; protein function evolution

资金

  1. National Human Genome Research Institute [U41HG002273]
  2. National Science Foundation [1917302]
  3. Div Of Biological Infrastructure
  4. Direct For Biological Sciences [1917302] Funding Source: National Science Foundation

向作者/读者索取更多资源

PANTHER is a user-focused knowledgebase that stores results of extensive phylogenetic reconstruction pipelines and provides manual review and annotation of function evolution events, aiding in protein sequence analysis tasks.
Phylogenetics is a powerful tool for analyzing protein sequences, by inferring their evolutionary relationships to other proteins. However, phylogenetics analyses can be challenging: they are computationally expensive and must be performed carefully in order to avoid systematic errors and artifacts. Protein Analysis THrough Evolutionary Relationships (PANTHER; ) is a publicly available, user-focused knowledgebase that stores the results of an extensive phylogenetic reconstruction pipeline that includes computational and manual processes and quality control steps. First, fully reconciled phylogenetic trees (including ancestral protein sequences) are reconstructed for a set of reference protein sequences obtained from fully sequenced genomes of organisms across the tree of life. Second, the resulting phylogenetic trees are manually reviewed and annotated with function evolution events: inferred gains and losses of protein function along branches of the phylogenetic tree. Here, we describe in detail the current contents of PANTHER, how those contents are generated, and how they can be used in a variety of applications. The PANTHER knowledgebase can be downloaded or accessed via an extensive API. In addition, PANTHER provides software tools to facilitate the application of the knowledgebase to common protein sequence analysis tasks: exploring an annotated genome by gene function; performing enrichment analysis of lists of genes; annotating a single sequence or large batch of sequences by homology; and assessing the likelihood that a genetic variant at a particular site in a protein will have deleterious effects.

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