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    | Request for Proposals |  
    | The Cancer Center has earmarked a total of $10,000 for next-generation sequencing services
    to support oncology research at Tufts Medical Center or Tufts University.  The funding must be expensed by August 31, 2011.
    The Internal Selection Committee, made up of members of the Cancer Center Executive Committee (CCEC), will
    select the project(s) based on scientific merit.   The application process: 
     
      Due Date: Friday, May 27, 2011 by 5:00pmApplication: Research title, list of investigators, sequencing ervices financial support required and research abstract (no more than one page)Email applications to: cancercenter@tuftsmedicalcenter.org |   |  
    | The GIMS Core currently has an Illumina HiSeq2000 and Roche 454 GS FLX, with plans to acquire either an Ion Torrent PGM or Illumina MiSeq in the near future.
      The Illumina HiSeq2000 can generate 200 gigabases of sequence data per week, and is the premier platform for whole genome and transcriptome sequencing.
      More information about the service (and next generation sequencing in general) is available at http://genomics.med.tufts.edu.
      Additional information about the Illumina system can also be found at http://www.illumina.com. One of the increasingly popular approaches to cancer research is whole exome capture followed by next generation sequencing.
      Capturing the exome leads to a much smaller library size, so several samples can be mixed into one lane of the sequencer,
      saving money while also targeting SNPs and other variations of interest.
      The Core offers exon capture via the NimbleGen SeqCap (http://www.nimblegen.com/products/seqcap/ez/v2/),
      Agilent SureSelect XT (http://www.genomics.agilent.com/),
      or Illumina TruSeq (http://www.illumina.com/products/truseq_exome_enrichment_kit.ilmn) methods as a service.
      The Core is happy to advise / consult if investigators prefer to obtain the kits and do the library preparation themselves. For questions regarding next-generation sequencing services and consultation on the cost of services, please contact Kip Bodi at x6-3763 or kip.bodi@tufts.edu. |  EventsTUCF Genomics sponsors a variety of events to promote the applications of next-generation sequencing
technologies at Tufts. 
| Past Events |  
    | Next Generation Sequencing and Applications for Transcriptome StudiesSponsored by Tufts CTSI, TMC, UIT, CNR, and TUCFWednesday, March 23 2011
 Sackler 216A
 
 The Computational Biology Initiative group at Tufts invites you to a half-day informal
      symposium on applications of next generation sequencing technology. The program
      includes invited talks from Tufts/TMC researchers and speakers from the Broad
      Institute and Merck, Inc. Please RSVP to Nina Bonnoyer
      to ensure an accurate head-count for lunch. Speakers:Lax Iyer, Tufts / TMC Mike Zody, Broad Institute
 Kip Bodi, Tufts
 Joshua Ainsley, Tufts
 Gavin Schnitzler, Tufts / TMC
 Adnan Derti, Merck Inc.
 
 |   |  
    | Agilent SureSelect SeminarSponsored by TUCF and AgilentWednesday, February 9 2011
 M&V 702
 
 Leveraging our ability to make high quality, long oligos, Agilent
      has created a genomic solution to enrich for regions of interest
      prior to next generation sequencing and analysis. This allows for
      greater depth of coverage for more samples, while saving
      sequencing dollars and time. This talk will review Agilent’s
      complete solution, and highlight our products by providing
      sequencing data. Speaker:Scott D. Leppanen, Ph.D., Field Applications Scientist, Agilent Technologies |   |  
    | GenomeQuest SeminarSponsored by TUCF and GenomeQuestWednesday, October 13 2010
 M&V 702
 
 GenomeQuest, the global leader in sequence data management, helps life science organizations realize the full promise of genomics.
      Over 160 leading health and agriculture companies use GenomeQuest for mission-critical work, including nine of the top ten pharmaceuticals.
      The core technology of the company is the GQ-Engine - a sequence database engine that is purpose-built for storing, managing, and analyzing NGS sequence data at whole- and multi-genome scale. Speaker:Dr. Kamalakar Gulukota, Senior Director, GenomeQuest, Inc. |  |  
    | Genomic Sequencing SymposiumSponsored by TUCF and IlluminaFriday, May 28 2010
 DeBlois Auditorium
 
 The Tufts Community is cordially invited to a Genomic Sequencing Symposium sponsored by Tufts University Core Facility and Illumina.
      Come learn about the field of genomic sequencing and it's many applications, including whole transcriptome sequencing, whole genome sequencing,
      and probing genetic networks. Presenters include local Tufts researchers, Andrew Camilli and Alex Ensminger, as well as the Director of
      Illumina R&D, Gary Schroth. Reception to follow with appetizers, refreshments, and opportunities to speak with the presenters and network
      with other genomic researchers    Speakers:  
        Gary Schroth, Ph.D.Senior Director of Gene Expression and Regulation Applications R&D, Illumina Inc.
 "Analysis of the Human Transcriptome by Next-Gen Sequencing"
 
 
        Andrew Camilli, Ph.D.Tufts University School of Medicine and Howard Hughes Medical Institute
 "Use of Massively Parallel Sequencing for Probing Genetic Networks"
 
 
        Alex Ensminger, Ph.D.Tufts University School of Medicine
 "Whole Genome Resequencing of Experimentally Adapted Legionella"
 
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