• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

PscanChIP:在 ChIP-Seq 实验的序列中发现过表达的转录因子结合位点基序及其相关性。

PscanChIP: Finding over-represented transcription factor-binding site motifs and their correlations in sequences from ChIP-Seq experiments.

机构信息

Dipartimento di Bioscienze, Università di Milano, Via Celoria 26, 20133 Milano, Italy.

出版信息

Nucleic Acids Res. 2013 Jul;41(Web Server issue):W535-43. doi: 10.1093/nar/gkt448. Epub 2013 Jun 7.

DOI:10.1093/nar/gkt448
PMID:23748563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3692095/
Abstract

Chromatin immunoprecipitation followed by sequencing with next-generation technologies (ChIP-Seq) has become the de facto standard for building genome-wide maps of regions bound by a given transcription factor (TF). The regions identified, however, have to be further analyzed to determine the actual DNA-binding sites for the TF, as well as sites for other TFs belonging to the same TF complex or in general co-operating or interacting with it in transcription regulation. PscanChIP is a web server that, starting from a collection of genomic regions derived from a ChIP-Seq experiment, scans them using motif descriptors like JASPAR or TRANSFAC position-specific frequency matrices, or descriptors uploaded by users, and it evaluates both motif enrichment and positional bias within the regions according to different measures and criteria. PscanChIP can successfully identify not only the actual binding sites for the TF investigated by a ChIP-Seq experiment but also secondary motifs corresponding to other TFs that tend to bind the same regions, and, if present, precise positional correlations among their respective sites. The web interface is free for use, and there is no login requirement. It is available at http://www.beaconlab.it/pscan_chip_dev.

摘要

染色质免疫沉淀结合新一代测序技术(ChIP-Seq)已成为构建特定转录因子(TF)结合基因组区域图谱的事实上的标准。然而,所鉴定的区域必须进一步进行分析,以确定 TF 的实际 DNA 结合位点,以及属于同一 TF 复合物或一般在转录调控中与其合作或相互作用的其他 TF 的结合位点。PscanChIP 是一个 Web 服务器,它从 ChIP-Seq 实验中获得的一组基因组区域开始,使用 JASPAR 或 TRANSFAC 位置特异性频率矩阵等 motif 描述符,或用户上传的描述符对它们进行扫描,并根据不同的测量和标准评估区域内的 motif 富集和位置偏向。PscanChIP 不仅可以成功识别 ChIP-Seq 实验中研究的 TF 的实际结合位点,还可以识别对应于其他倾向于结合相同区域的 TF 的二级 motif,如果存在的话,还可以识别它们各自位点之间的精确位置相关性。该 Web 界面可免费使用,无需登录。它可在 http://www.beaconlab.it/pscan_chip_dev 上获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/3753cd59643d/gkt448f3ap.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/5f8be3191ee6/gkt448f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/58bb34caf657/gkt448f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/3753cd59643d/gkt448f3ap.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/5f8be3191ee6/gkt448f1p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/58bb34caf657/gkt448f2p.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3de1/3692095/3753cd59643d/gkt448f3ap.jpg

相似文献

1
PscanChIP: Finding over-represented transcription factor-binding site motifs and their correlations in sequences from ChIP-Seq experiments.PscanChIP:在 ChIP-Seq 实验的序列中发现过表达的转录因子结合位点基序及其相关性。
Nucleic Acids Res. 2013 Jul;41(Web Server issue):W535-43. doi: 10.1093/nar/gkt448. Epub 2013 Jun 7.
2
Using Weeder, Pscan, and PscanChIP for the Discovery of Enriched Transcription Factor Binding Site Motifs in Nucleotide Sequences.使用Weeder、Pscan和PscanChIP在核苷酸序列中发现富集的转录因子结合位点基序。
Curr Protoc Bioinformatics. 2014 Sep 8;47:2.11.1-31. doi: 10.1002/0471250953.bi0211s47.
3
Differential motif enrichment analysis of paired ChIP-seq experiments.配对染色质免疫沉淀测序(ChIP-seq)实验的差异基序富集分析
BMC Genomics. 2014 Sep 2;15(1):752. doi: 10.1186/1471-2164-15-752.
4
Inferring direct DNA binding from ChIP-seq.从 ChIP-seq 推断直接 DNA 结合。
Nucleic Acids Res. 2012 Sep 1;40(17):e128. doi: 10.1093/nar/gks433. Epub 2012 May 18.
5
MEME-ChIP: motif analysis of large DNA datasets.MEME-ChIP:大 DNA 数据集的基序分析。
Bioinformatics. 2011 Jun 15;27(12):1696-7. doi: 10.1093/bioinformatics/btr189. Epub 2011 Apr 12.
6
iTAR: a web server for identifying target genes of transcription factors using ChIP-seq or ChIP-chip data.iTAR:一个利用ChIP-seq或ChIP-chip数据识别转录因子靶基因的网络服务器。
BMC Genomics. 2016 Aug 12;17(1):632. doi: 10.1186/s12864-016-2963-0.
7
Improving analysis of transcription factor binding sites within ChIP-Seq data based on topological motif enrichment.基于拓扑基序富集改进ChIP-Seq数据中转录因子结合位点的分析。
BMC Genomics. 2014 Jun 13;15(1):472. doi: 10.1186/1471-2164-15-472.
8
Cscan: finding common regulators of a set of genes by using a collection of genome-wide ChIP-seq datasets.Cscan:通过使用一组全基因组 ChIP-seq 数据集来发现一组基因的常见调控因子。
Nucleic Acids Res. 2012 Jul;40(Web Server issue):W510-5. doi: 10.1093/nar/gks483. Epub 2012 Jun 4.
9
Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors.119 个人类转录因子结合的基因组区域的序列特征和染色质结构。
Genome Res. 2012 Sep;22(9):1798-812. doi: 10.1101/gr.139105.112.
10
A new exhaustive method and strategy for finding motifs in ChIP-enriched regions.一种在 ChIP 富集区域中寻找基序的全新穷举方法和策略。
PLoS One. 2014 Jan 24;9(1):e86044. doi: 10.1371/journal.pone.0086044. eCollection 2014.

引用本文的文献

1
Bone morphogenetic protein (BMP) signaling determines neuroblastoma cell fate and sensitivity to retinoic acid.骨形态发生蛋白(BMP)信号决定神经母细胞瘤细胞的命运以及对视黄酸的敏感性。
Nat Commun. 2025 Feb 28;16(1):2036. doi: 10.1038/s41467-025-57185-y.
2
Emerging cooperativity between Oct4 and Sox2 governs the pluripotency network in early mouse embryos.Oct4和Sox2之间新出现的协同作用调控小鼠早期胚胎中的多能性网络。
Elife. 2025 Feb 27;13:RP100735. doi: 10.7554/eLife.100735.
3
Comprehensive analysis of computational approaches in plant transcription factors binding regions discovery.

本文引用的文献

1
NF-Y coassociates with FOS at promoters, enhancers, repetitive elements, and inactive chromatin regions, and is stereo-positioned with growth-controlling transcription factors.NF-Y 与 FOS 在启动子、增强子、重复元件和非活性染色质区域共同结合,并与控制生长的转录因子立体定位。
Genome Res. 2013 Aug;23(8):1195-209. doi: 10.1101/gr.148080.112. Epub 2013 Apr 17.
2
Distinct transcriptional regulatory modules underlie STAT3's cell type-independent and cell type-specific functions.STAT3 的细胞类型非依赖性和细胞类型特异性功能由不同的转录调控模块所支撑。
Nucleic Acids Res. 2013 Feb 1;41(4):2155-70. doi: 10.1093/nar/gks1300. Epub 2013 Jan 7.
3
植物转录因子结合区域发现中计算方法的综合分析
Heliyon. 2024 Oct 10;10(20):e39140. doi: 10.1016/j.heliyon.2024.e39140. eCollection 2024 Oct 30.
4
The evaluation of transcription factor binding site prediction tools in human and Arabidopsis genomes.人类和拟南芥基因组中转录因子结合位点预测工具的评估
BMC Bioinformatics. 2024 Dec 2;25(1):371. doi: 10.1186/s12859-024-05995-0.
5
PTFSpot: deep co-learning on transcription factors and their binding regions attains impeccable universality in plants.PTFSpot:在转录因子及其结合区域上进行深度协同学习,在植物中实现了完美的通用性。
Brief Bioinform. 2024 May 23;25(4). doi: 10.1093/bib/bbae324.
6
A PPARγ/long noncoding RNA axis regulates adipose thermoneutral remodeling in mice.过氧化物酶体增殖物激活受体 γ/长非编码 RNA 轴调控小鼠脂肪组织恒温重塑。
J Clin Invest. 2023 Nov 1;133(21):e170072. doi: 10.1172/JCI170072.
7
B lymphocytes in treatment-naive paediatric patients with lupus are epigenetically distinct from healthy children.治疗初发的狼疮患儿的 B 淋巴细胞在表观遗传学上有别于健康儿童。
Lupus Sci Med. 2023 May;10(1). doi: 10.1136/lupus-2023-000921.
8
Redistribution of lamina-associated domains reshapes binding of pioneer factor FOXA2 in development of nonalcoholic fatty liver disease.层粘连相关结构域的再分布重塑了先驱因子 FOXA2 在非酒精性脂肪性肝病发生过程中的结合。
Genome Res. 2022 Nov-Dec;32(11-12):1981-1992. doi: 10.1101/gr.277149.122. Epub 2022 Dec 15.
9
Combinatorial targeting of a chromatin complex comprising Dot1L, menin and the tyrosine kinase BAZ1B reveals a new therapeutic vulnerability of endocrine therapy-resistant breast cancer.组合靶向包含 Dot1L、menin 和酪氨酸激酶 BAZ1B 的染色质复合物揭示了内分泌治疗耐药性乳腺癌的新治疗弱点。
Breast Cancer Res. 2022 Jul 18;24(1):52. doi: 10.1186/s13058-022-01547-7.
10
Commensal segmented filamentous bacteria-derived retinoic acid primes host defense to intestinal infection.共生节状丝状菌衍生的视黄酸激活宿主防御以抵抗肠道感染。
Cell Host Microbe. 2021 Dec 8;29(12):1744-1756.e5. doi: 10.1016/j.chom.2021.09.010. Epub 2021 Oct 21.
ENCODE data in the UCSC Genome Browser: year 5 update.
在 UCSC 基因组浏览器中编码数据:第 5 年更新。
Nucleic Acids Res. 2013 Jan;41(Database issue):D56-63. doi: 10.1093/nar/gks1172. Epub 2012 Nov 27.
4
ChIP-seq and beyond: new and improved methodologies to detect and characterize protein-DNA interactions.ChIP-seq 及其他方法:检测和描述蛋白质-DNA 相互作用的新方法和改进方法。
Nat Rev Genet. 2012 Dec;13(12):840-52. doi: 10.1038/nrg3306. Epub 2012 Oct 23.
5
Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors.119 个人类转录因子结合的基因组区域的序列特征和染色质结构。
Genome Res. 2012 Sep;22(9):1798-812. doi: 10.1101/gr.139105.112.
6
Architecture of the human regulatory network derived from ENCODE data.人类调控网络的结构源自 ENCODE 数据。
Nature. 2012 Sep 6;489(7414):91-100. doi: 10.1038/nature11245.
7
Inferring direct DNA binding from ChIP-seq.从 ChIP-seq 推断直接 DNA 结合。
Nucleic Acids Res. 2012 Sep 1;40(17):e128. doi: 10.1093/nar/gks433. Epub 2012 May 18.
8
Motif discovery and transcription factor binding sites before and after the next-generation sequencing era. motif 发现和转录因子结合位点在新一代测序时代前后。
Brief Bioinform. 2013 Mar;14(2):225-37. doi: 10.1093/bib/bbs016. Epub 2012 Apr 19.
9
Cell-type specific and combinatorial usage of diverse transcription factors revealed by genome-wide binding studies in multiple human cells.通过在多种人类细胞中的全基因组结合研究揭示了多样化转录因子的细胞类型特异性和组合性使用。
Genome Res. 2012 Jan;22(1):9-24. doi: 10.1101/gr.127597.111. Epub 2011 Nov 16.
10
CENTDIST: discovery of co-associated factors by motif distribution.CENTDIST:通过基序分布发现共相关因子。
Nucleic Acids Res. 2011 Jul;39(Web Server issue):W391-9. doi: 10.1093/nar/gkr387. Epub 2011 May 20.