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BAC, PAC, Cosmid, Fosmid Sequencing

High throughput end sequencing of clones from both sides by state-of-the-art Sanger technology on ABI 3730XL sequencers.

Eurofins MWG Operon is offering coverage sequencing of defined BAC clones by Genome Sequencerâ„¢ FLX Titanium reagents or ABI 3730 XL technology and closing of gaps by primer walking.

Benfit from our BAC, PAC, Cosmid & Fosmid Sequencing

We offer High Throughput Screening by End-Sequencing of BAC, PAC, Fosmid or Cosmid Clones by Sanger Sequencing

  • Clones can be delivered as stab or glycerol cultures in microtiter plates
  • Preparation of the clones and sequencing from both ends
  • Ideal for creating physical maps (minimal tiling path)
  • Ideal for scaffolding of contigs in genome sequencing projects.

Coverage Sequencing of BAC Clones by GS FLX

  • Clones can be delivered as stab or glycerol cultures
  • DNA preparation
  • Generation of the shotgun library and emPCR (emulsion PCR)
  • High throughput sequencing
  • Assembly of the sequence reads.

Physical Gap Closure of BAC Clones

  • Scaffolding and final gap closure by various PCR approaches and primer walking steps on the BAC DNA
  • Additional bioinformatic services on request.

Shotgun Sequencing of BAC, PAC, Cosmid, Fosmid Clones by Sanger Sequencing

  • Clones can be delivered as stab or glycerol cultures
  • DNA preparation
  • Generation of shotgun plasmid libraries
  • High throughput Sanger sequencing until requested coverage is reached
  • Assembly of the sequence reads.

Physical Gap Closure

  • Final gap closure by various PCR approaches and primer walking steps on the BAC, PAC, Cosmid or Fosmid DNA
  • Additional bioinformatic services on request.

Your Advantages

  • Fast turnaround times
  • Experience resulting from the completion of more than 1500 BAC sequencing projects
  • Project consultancy and support
  • Storage of material and data
  • Bioinformatic services.

 

Certified Service Provider

Genomic enrichment using the complete NimbleGen Sequence Capture workflow optimised for GS FLX sequencing

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