Mercurial > repos > john-mccallum > pcr_markers
diff README.md @ 5:b321e0517be3 draft
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author | ben-warren |
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date | Thu, 22 May 2014 20:30:19 -0400 |
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children | f201e8c6e004 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/README.md Thu May 22 20:30:19 2014 -0400 @@ -0,0 +1,24 @@ +galaxy-pcr-markers +================== + +Scripts for design of PCR-based Marker Assays from DNA sequence variant data, and xml wrappers for use in Galaxy workflow environment + +Also available for download at Galaxy Toolshed http://toolshed.g2.bx.psu.edu/ +hg clone http://toolshed.g2.bx.psu.edu/repos/john-mccallum/pcr_markers + +NOTE that the primer design tool *design_primers.py* relies on EMBOSS ePrimer3 which depends on Primer3 1.1.4. +The updated tool *design_HRM_primers.py* does not have this restriction and should work with Primer3 V2. + +Please see development branch HRM for optimised design of high-resolution melting PCR assays using the uMelt web service at University of Utah. + + +**CITATION** +A Toolkit For Bulk PCR-Based Marker Design From Next-Generation Sequence Data: Application For Development Of A Framework Linkage Map In Bulb Onion (Allium cepa L.) (2012) + +Samantha Baldwin, Roopashree Revanna, Susan Thomson, Meeghan Pither-Joyce, Kathryn Wright, Ross Crowhurst, Mark Fiers, Leshi Chen, Richard MacKnight, John A. McCallum + +BMC Genomics 2012, 13:637 http://www.biomedcentral.com/1471-2164/13/637/abstract + +**Acknowledgements** +Current development of these tools is funded by the New Zealand Ministry for Business, Innovation & Employment project 'Virtual Institute of Statistical Genetics' (VISG) +See http://www.visg.co.nz