Mercurial > repos > mkhan1980 > ctcf_analysis
view check.xml @ 4:c30f1e611791 draft
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author | mkhan1980 |
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date | Mon, 04 Mar 2013 07:01:24 -0500 |
parents | e3c4e5ff7f74 |
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<tool id="fa_gc_content_1" name="Discover CTCF Sites for Forward Strand"> <description></description> <command interpreter="perl">check.pl $input $input2 $output</command> <inputs> <param format="fasta" name="input" type="data" label="Forward Strand Sequence File"/> <param format="fasta" name="input2" type="data" label="Forward Strand Coordinate file"/> </inputs> <outputs> <data format="tabular" name="output" /> </outputs> <tests> <test> <param name="input" value="fa_gc_content_input.fa"/> <param name="input2" value="fa_gc_content_input2.fa"/> <output name="out_file1" file="concatenated.txt"/> </test> </tests> <help> Background: This tool computationally predicts CTCF sites for a nucleotide sequence located on the forward strand. The user is required to provide two files as inputs. The first is the nucleotide sequence of interest on the + strand in FASTA format (this can be obtained from UCSC genome browser or Ensembl). The second file must be a FASTA formatted file containing the chromosome number and the genomic position of the first nucleotide sequence (separated by a tab). For example, if the sequence of interest is located on chromosome 3 with a starting genomic position of 1850000, the first line of the second input file must start with a fasta tag, and the second line will be chr3 1850000 Details of Algorithm: CTCF sites are predicted by applying the following equation w(σ,j) = log2 (((f(σ,j) + sqrt(N) x b(σ)) / (N + sqrt(N))) / b(σ)) Where w(σ,j) is the weight of nucleotide σ at position j, N is the total number of binding sites or the sum of all nucleotide occurrences in the column, and b is the prior background frequency of the nucleotide σ. The sum of weights for corresponding nucleotides at each column of the matrix then estimates the likelihood of any sequence of length m to be an instance of a CTCF binding site and takes into account the GC content of the genomic region being scanned. Citation and further help: For further details of the algorithm, please refer to Khan MA, Soto-Jimenez LM, Howe T, Streit A, Sosinsky A, Stern CD (2013). Computational tools and resources for prediction and analysis of gene regulatory regions in the chick genome.. Genesis, , - . doi:10.1002/dvg.22375 For queries/questions, email ucbtmaf@ucl.ac.uk </help> </tool>