FYI.... Sean
---------- Forwarded message ---------- From: Young, Lynn (NIH/OD/ORS) [E] <[email protected]> Date: Thu, Jun 18, 2015 at 3:58 PM Subject: June 24 – Golden Helix: SNP & Variation Suite (SVS) and VarSeq Golden Helix: SNP & Variation Suite (SVS) and VarSeq June 24, 2015, 9 a.m. – 4 p.m. NIH Library Training Room Registration required The NIH Library Bioinformatics Support Program <http://t.signauxsix.com/e1t/c/5/f18dQhb0S7lC8dDMPbW2n0x6l2B9nMJW7t5XX48p-Yr4W2m646p3VXKlsF3y7_BYm2_qf9fsnwg03?t=http%3A%2F%2Fnihlibrary.nih.gov%2FServices%2FBioinformatics%2FPages%2Fdefault.aspx&si=4782978249523200&pi=13c85b25-2e24-4a7e-b6f7-d217d52dd1c1> is presenting a “Data Analysis on Microarray and NGS Data in Golden Helix SNP & Variation Suite (SVS) and VarSeq” class for June 24. The free training will be held in the NIH Library Training Room, Building 10, from 9 a.m. to 4 p.m. Registration is required (use the link provided below). The morning class will begin with an overview lecture/demo focusing on SNP GWAS analysis and population-based NGS analysis workflows. Following the demo will be a hands-on session during which attendees will use SNP & Variation Suite (SVS). The afternoon session will begin with an overview lecture/demo focusing on small-n NGS dataset analysis. Following the demo there will be a hands-on session during which attendees will use VarSeq to analyze gene panel and whole exome trio data to identify variants of interest. This class will be taught by Golden Helix research staff and is open to NIH staff. For more information on how to access the NIH Library license for SNP & Variation Suite (SVS) and VarSeq, please visit http://nihlibrary.nih.gov/Services/Bioinformatics/Pages/bioanalysis.aspx. For further information about the class and to register, visit http://nihlibrary.beta.libcal.com/event/2053637. ------------------------------ To unsubscribe from the BIOINFORMATICS-SIG-L list, click the following link: http://list.nih.gov/cgi-bin/wa.exe?SUBED1=BIOINFORMATICS-SIG-L&A=1
