Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

General information

URL: http://ac.agrogene.ac.cn/utr
Full name: Alternative Poly(A) Sites database 2.0
Description: A web-accessible database, named APASdb, which can visualize the precise map and usage quantification of different APA isoforms for all genes. The datasets are deeply profiled by the sequencing alternative polyadenylation sites (SAPAS) method capable of high-throughput sequencing 3'-ends of polyadenylated transcripts. Thus, APASdb details all the heterogeneous cleavage sites downstream of poly(A) signals, and maintains near complete coverage for APA sites, much better than the previous databases using conventional methods. Furthermore, APASdb provides the quantification of a given APA variant among transcripts with different APA sites by computing their corresponding normalized-reads, making our database more useful. In addition, APASdb supports URL-based retrieval, browsing and display of exon-intron structure, poly(A) signals, poly(A) sites location and usage reads, and 3'-untranslated regions (3'-UTRs).
Year founded: 2014
Last update: 2023
Version: v2
Accessibility:
Manual:
Accessible
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Country/Region: China

Contact information

University/Institution: Beijing University of Chinese Medine
Address: No. 11 Dong San Huang Road, Chao-yang District, Beijing 100029, China
City: Beijing
Province/State:
Country/Region: China
Contact name (PI/Team): Leiming YOU
Contact email (PI/Helpdesk): youleiming@bucm.edu.cn

Publications

25378337
APASdb: a database describing alternative poly(A) sites and selection of heterogeneous cleavage sites downstream of poly(A) signals. [PMID: 25378337]
You L, Wu J, Feng Y, Fu Y, Guo Y, Long L, Zhang H, Luan Y, Tian P, Chen L, Huang G, Huang S, Li Y, Li J, Chen C, Zhang Y, Chen S, Xu A.

Increasing amounts of genes have been shown to utilize alternative polyadenylation (APA) 3'-processing sites depending on the cell and tissue type and/or physiological and pathological conditions at the time of processing, and the construction of genome-wide database regarding APA is urgently needed for better understanding poly(A) site selection and APA-directed gene expression regulation for a given biology. Here we present a web-accessible database, named APASdb (http://mosas.sysu.edu.cn/utr), which can visualize the precise map and usage quantification of different APA isoforms for all genes. The datasets are deeply profiled by the sequencing alternative polyadenylation sites (SAPAS) method capable of high-throughput sequencing 3'-ends of polyadenylated transcripts. Thus, APASdb details all the heterogeneous cleavage sites downstream of poly(A) signals, and maintains near complete coverage for APA sites, much better than the previous databases using conventional methods. Furthermore, APASdb provides the quantification of a given APA variant among transcripts with different APA sites by computing their corresponding normalized-reads, making our database more useful. In addition, APASdb supports URL-based retrieval, browsing and display of exon-intron structure, poly(A) signals, poly(A) sites location and usage reads, and 3'-untranslated regions (3'-UTRs). Currently, APASdb involves APA in various biological processes and diseases in human, mouse and zebrafish. © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research.

Nucleic Acids Res. 2015:43(Database issue) | 45 Citations (from Europe PMC, 2024-04-27)

Ranking

All databases:
1740/6000 (71.017%)
Gene genome and annotation:
530/1675 (68.418%)
Expression:
355/1143 (69.029%)
Modification:
101/287 (65.157%)
1740
Total Rank
45
Citations
5
z-index

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Record metadata

Created on: 2023-04-07
Curated by:
Leiming YOU [2023-04-11]
Lin Liu [2023-04-10]
Leiming YOU [2023-04-07]