APASdb: a database describing alternative poly(A) sites and selection of heterogeneous cleavage sites downstream of poly(A) signals.
APASdb: a database describing alternative poly(A) sites and selection of heterogeneous cleavage sites downstream of poly(A) signals.
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DOI:
10.1093/nar/gku1076
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发表时间:
2015-01
影响因子:
14.9
通讯作者:
Xu A
中科院分区:
文献类型:
--
作者:
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.
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DOI:
10.1093/database/bau076
发表时间:
2014-07-22
影响因子:
5.8
作者:
Mueller, Soeren;Rycak, Lukas;Rotter, Bjoern
通讯作者:
Rotter, Bjoern
影响因子:
12.3
作者:
Langmead B;Schatz MC;Lin J;Pop M;Salzberg SL
通讯作者:
Salzberg SL
影响因子:
14.9
作者:
Grillo G;Turi A;Licciulli F;Mignone F;Liuni S;Banfi S;Gennarino VA;Horner DS;Pavesi G;Picardi E;Pesole G
通讯作者:
Pesole G
影响因子:
14.9
作者:
Tian B;Hu J;Zhang H;Lutz CS
通讯作者:
Lutz CS
影响因子:
7
作者:
Beaudoing, E;Gautheret, D
通讯作者:
Gautheret, D