Sole-Search: An integrated analysis program for peak detection and functional annotation using ChIP-seq data
Nucleic Acids Research, ISSN: 0305-1048, Vol: 38, Issue: 3, Page: e13
2009
- 99Citations
- 179Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations99
- Citation Indexes99
- 99
- CrossRef83
- Captures179
- Readers179
- 179
- Mentions1
- References1
- Wikipedia1
Article Description
Next-generation sequencing is revolutionizing the identification of transcription factor binding sites throughout the human genome. However, the bioinformatics analysis of large datasets collected using chromatin immunoprecipitation and high-throughput sequencing is often a roadblock that impedes researchers in their attempts to gain biological insights from their experiments. We have developed integrated peak-calling and analysis software (Sole-Search) which is available through a user-friendly interface and (i) converts raw data into a format for visualization on a genome browser, (ii) outputs ranked peak locations using a statistically based method that overcomes the significant problem of false positives, (iii) identifies the gene nearest to each peak, (iv) classifies the location of each peak relative to gene structure, (v) provides information such as the number of binding sites per chromosome and per gene and (vi) allows the user to determine overlap between two different experiments. In addition, the program performs an analysis of amplified and deleted regions of the input genome. This software is web-based and automated, allowing easy and immediate access to all investigators. We demonstrate the utility of our software by collecting, analyzing and comparing ChIP-seq data for six different human transcription factors/cell line combinations. © The Author(s) 2009. Published by Oxford University Press.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77951230100&origin=inward; http://dx.doi.org/10.1093/nar/gkp1012; http://www.ncbi.nlm.nih.gov/pubmed/19906703; https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/gkp1012; https://dx.doi.org/10.1093/nar/gkp1012; https://academic.oup.com/nar/article/38/3/e13/3112335; http://europepmc.org/abstract/med/19906703; http://europepmc.org/articles/PMC2817454; https://academic.oup.com/nar/article-pdf/38/3/e13/16768013/gkp1012.pdf; http://nar.oxfordjournals.org/lookup/doi/10.1093/nar/gkp1012; http://nar.oxfordjournals.org/content/38/3/e13
Oxford University Press (OUP)
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