POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins.
POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins.
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POSTAR3:用于探索 RNA 结合蛋白协调的转录后调控的更新平台
DOI:
10.1093/nar/gkab702
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发表时间:
2022-01-07
影响因子:
14.9
通讯作者:
Lu ZJ
中科院分区:
文献类型:
--
作者:
Zhao W;Zhang S;Zhu Y;Xi X;Bao P;Ma Z;Kapral TH;Chen S;Zagrovic B;Yang YT;Lu ZJ
Abstract RNA-binding proteins (RBPs) play key roles in post-transcriptional regulation. Accurate identification of RBP binding sites in multiple cell lines and tissue types from diverse species is a fundamental endeavor towards understanding the regulatory mechanisms of RBPs under both physiological and pathological conditions. Our POSTAR annotation processes make use of publicly available large-scale CLIP-seq datasets and external functional genomic annotations to generate a comprehensive map of RBP binding sites and their association with other regulatory events as well as functional variants. Here, we present POSTAR3, an updated database with improvements in data collection, annotation infrastructure, and analysis that support the annotation of post-transcriptional regulation in multiple species including: we made a comprehensive update on the CLIP-seq and Ribo-seq datasets which cover more biological conditions, technologies, and species; we added RNA secondary structure profiling for RBP binding sites; we provided miRNA-mediated degradation events validated by degradome-seq; we included RBP binding sites at circRNA junction regions; we expanded the annotation of RBP binding sites, particularly using updated genomic variants and mutations associated with diseases. POSTAR3 is freely available at http://postar.ncrnalab.org.
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影响因子:
12.3
作者:
Friedersdorf MB;Keene JD
通讯作者:
Keene JD
影响因子:
64.8
作者:
GTEx Consortium;Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group;Statistical Methods groups—Analysis Working Group;Enhancing GTEx (eGTEx) groups;NIH Common Fund;NIH/NCI;NIH/NHGRI;NIH/NIMH;NIH/NIDA;Biospecimen Collection Source Site—NDRI;Biospecimen Collection Source Site—RPCI;Biospecimen Core Resource—VARI;Brain Bank Repository—University of Miami Brain Endowment Bank;Leidos Biomedical—Project Management;ELSI Study;Genome Browser Data Integration &Visualization—EBI;Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California Santa Cruz;Lead analysts:;Laboratory, Data Analysis &Coordinating Center (LDACC):;NIH program management:;Biospecimen collection:;Pathology:;eQTL manuscript working group:;Battle A;Brown CD;Engelhardt BE;Montgomery SB
通讯作者:
Montgomery SB
影响因子:
9.2
作者:
Addo-Quaye, Charles;Eshoo, Tifani W.;Axtell, Michael J.
通讯作者:
Axtell, Michael J.
影响因子:
11.8
作者:
Gregory, Brian D.;O'Malley, Ronan C.;Ecker, Joseph R.
通讯作者:
Ecker, Joseph R.
影响因子:
64.8
作者:
Ghandi, Mahmoud;Huang, Franklin W.;Sellers, William R.
通讯作者:
Sellers, William R.