Li Lab:Softwares: Difference between revisions
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*[http://ceas.cbi.pku.edu.cn/ Cis-regulatory Element Annotation System (CEAS)] | *[http://ceas.cbi.pku.edu.cn/ Cis-regulatory Element Annotation System (CEAS)] | ||
An integrated webserver for analyzing ChIP-chip data | An integrated webserver for analyzing ChIP-chip data | ||
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* [http://code.google.com/p/ | * [http://code.google.com/p/bseqc/ BSeQC: Quality Control of Bisulfite Sequencing Experiments] | ||
* [http://code.google.com/p/dychips/ DyChIPS: An integrate solution for dynamic analysis of ChIP-sequencing] | * [http://code.google.com/p/dychips/ DyChIPS: An integrate solution for dynamic analysis of ChIP-sequencing] | ||
DyChIPS is designed for comparative analysis of ChIPSeq data whose targets tend to be broad and are widely distributed across the genome, such as histone modification or some chromatin-binding proteins. | DyChIPS is designed for comparative analysis of ChIPSeq data whose targets tend to be broad and are widely distributed across the genome, such as histone modification or some chromatin-binding proteins. |
Revision as of 22:25, 7 April 2013
A model-based algorithm for finding enriched regions in ChIP-Chip experiments
An integrated webserver for analyzing ChIP-chip data
A model-based algorithm for finding enriched regions in ChIP-Seq experiments.
BSMAP is the first general-purpose bisulfite mapping software. It is able to map high-throughput bisulfite reads at whole genome level with feasible memory and CPU usage.
RseQC comprehensively evaluatse different aspects of RNA-seq experiments, such as sequence quality, GC bias, PCR bias, nucleotide composition bias, sequencing depth, strand specificity, coverage uniformity, and read distribution over the genome structure.
DANPOS is specifically developed for comparison between nucleosome maps generated based on high-throughput sequencing, it detects changes in nucleosome position, occupancy, or fuzziness at single nucleotide resolution.
DyChIPS is designed for comparative analysis of ChIPSeq data whose targets tend to be broad and are widely distributed across the genome, such as histone modification or some chromatin-binding proteins.