AceView genes database
AceView genes database provides a non-redundant, integrated representation of all publicly available mRNA sequences, including single-pass cDNA and EST data, aggregated from GenBank, RefSeq, dbEST, and Trace archives for transcript structure and expression analysis.
Key Features:
- Non-Redundant Sequence Representation: Consolidates overlapping and duplicate mRNA and cDNA sequences to produce a streamlined, non-redundant dataset.
- Comprehensive Coverage: Aggregates sequences from GenBank, RefSeq, dbEST, and Trace archives, including single-pass cDNA and EST sources.
- Redundancy Elimination Algorithms: Applies advanced algorithms to identify and remove redundant sequences and models.
- Data Integration and Validation: Integrates data from multiple sources with rigorous quality control and validation to ensure sequence accuracy and reliability.
- Annotation Integration: Associates sequences with relevant annotations to provide contextual information for analyses.
Scientific Applications:
- Gene Expression Studies: Enables analysis of mRNA sequence diversity and expression patterns across tissues and conditions.
- Transcription Factor Binding Analysis: Supports studies of transcriptional regulation, including analyses involving STAT3 and IRF4 regulation of Prdm1 relevant to plasma cell differentiation and T cell homeostasis.
- Comparative Genomics: Facilitates identification of conserved elements and comparative analyses across species or gene families.
- Functional Genomics: Supports correlation of mRNA sequence variation with phenotypic effects, including cytokine-driven regulation such as IL-21 impacts on gene regulation and cellular differentiation.
Methodology:
Sequences are aggregated from GenBank, RefSeq, dbEST, and Trace archives; advanced algorithms are used to identify and remove redundant sequences; rigorous validation and quality-control procedures are applied; sequences are integrated with annotations.
Topics
Collections
Details
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Added:
- 9/11/2015
- Last Updated:
- 12/29/2018
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Query and retrieval
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Publications
Kwon H, Thierry-Mieg D, Thierry-Mieg J, Kim H, Oh J, Tunyaplin C, Carotta S, Donovan CE, Goldman ML, Tailor P, Ozato K, Levy DE, Nutt SL, Calame K, Leonard WJ. Analysis of Interleukin-21-Induced Prdm1 Gene Regulation Reveals Functional Cooperation of STAT3 and IRF4 Transcription Factors. Immunity. 2009;31(6):941-952. doi:10.1016/j.immuni.2009.10.008. PMID:20064451. PMCID:PMC3272079.