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Seq Monk 0.24.1 freeware

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SeqMonk is a powerful application designed to enable you to visualize and analyze mapped sequence data.

It was written for use with mapped next generation sequence data but can in theory be used for any dataset which can be expressed as a series of genomic positions. ...

Author Babraham Bioinformatics
Released 2013-02-25
Filesize 3.00 MB
Downloads 381
OS Windows XP, Windows Vista, Windows Vista x64, Windows 7, Windows 7 x64
Installation Instal And Uninstall
Keywords view sequence data, analyse sequence data, sequence data analysis, sequence data, view, analyse
Users' rating
(18 rating)
Seq MonkCADWindows XP, Windows Vista, Windows Vista x64, Windows 7, Windows 7 x64
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Seq Monk - analysis application Freeware Download Notice

Seq Monk Free Download - we do not host any Seq Monk torrent files or links of Seq Monk on rapidshare.com, depositfiles.com, megaupload.com etc. All Seq Monk download links are direct Seq Monk download from publisher site or their selected mirrors.

Seq Monk freeware - The Latest User Reviews
Seq Monk freeware - The Latest Versions History
0.24.1 Feb 25, 2013 New Release · Fixed a bug in RNA quantitation for unmerged transcripts
· Fixed a bug causing MACS user options to not be read
· Fixed a crash in the visible store parser
· Fixed an axis label layout bug in the probe trend plot
· Fixed a crash in the intensity difference filter when run with a very small list of probes
0.24.0 Feb 14, 2013 New Release · Added GFF export option to reports
· Added antisense transcription pipeline
· Added automatic feedback to crash reports
· Added an ID field to reports
· Added a probe length quantitation
· Added a smoothing subtraction quantitation
· Added a probe name filter
· Added the ability to do gene level RNA-Seq quantitation
· Added a Chi-Square contingency test statistical filter
· Added a raw count option to the RNA-Seq pipeline
· Added the ability to specify the order of highlighted sublists in the scatterplot
0.23.1 Dec 17, 2012 New Release · Fixed a bug causing crashing from invalid chromosome names in imported data
· Allowed per-chromosome normalisation in the cis/trans quantitation
· Added per-chromsome filtering to the cis/trans scatterplot
· Added an option to export valid interaction ends into a probe list to the HiC heatmaps

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