Computel is designed for measuring mean telomere length and abundance of canonical and variant telomeric repeats from Illumina Whole Genome NGS Sequencing data.
Computel versions > v0.3 work with Unix operating system (tested for Ubuntu Linux). Computel version v0.2 works with Windows and Unix operating systems, however this version is harder to apply.
Version v1.2 allows to change the quality threshold (default being Phred+33 25)
Version v1.1 computes telomeric variants with Phred+33 25 qual threshold.
Version v1.0 has an additional feature of computing the relative abundance of telomeric canonical and variant repeat patterns among the telomeric reads.
Version v0.4.1 has fixed a minor bug from the v0.4 release.
Version v0.4 works with shell script and has a straightforward usage. This version of Computel uses the samtools (version 1.3 or higher) installed on the user's system, instead of the precompiled version coming with the previous releases.
Version v0.3 works with shell script and has a straightforward usage.
Version v0.2 works also with compressed fastq files.
Version v0.1 works both Windows and Unix type operating systems, works with configuration files and Rscript. Works also with compressed fastq files.
You have to have R (version 3.0.3 or higher) and samtools version 1.3 or higher (for Computel v0.4) installed in your system.
For installation download and uncompress the Computel package in a local directory. The required binaries and files for setup configuration are set in the package. Make computel.sh executable by running 'chmod +x computel.sh'.
The basic usage is:
./computel.sh [options] -1 <fq1> -2 <fq2> -o <outputpath>
Note, Computel works with only some versions of Bowtie, and with Samtools version 1.3 or higher. You can specify your own binaries with respective options, however, you may first want to refer to the Computel User Manual.
Use the following citation to read about our software, and cite it in your research:
Nersisyan L, Arakelyan A (2015) Computel: Computation of Mean Telomere Length from Whole-Genome Next-Generation Sequencing Data. PLoS ONE 10(4): e0125201. doi:10.1371/journal.pone.0125201
This is the betta version of the software: your feedback at this point is critical for its further development! Please, join the Computel discussion group at https://groups.google.com/forum/#!forum/computel-discussion-forum, and add your comments. Please, do not hesitate to share any inconvenience you face with our software, any bug you notice and any suggestion you have.
If you're happy with Computel, let us know - make us happy too!