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NovoAlignCS

Designed to fully support reads from ABI SOLiD Color Space.

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Packed with features:

  1. Mapping with color quality values.
  2. Alignment quality scores using posterior alignment probability.
  3. Paired end alignment.
  4. Mismatches and gaps of up to 30% of read length for paired-end reads.
  5. Use of ambiguous codes in reference sequences can be used to reduce allelic bias.
  6. Automatic color quality calibration.
  7. Handles single end and paired end reads up to 100bp/read.

 

NovoAlignCSMPI – Enables the use of multiple servers in a cluster to align a file of reads.

  1. NovoAlignCSMPI version is available for purchase.

Note: NovoAlignCS and NovoAlignCSMPI are only available with a license.

 

System Requirements

Intel/AMD X86-64 CPU running a 64-bit Linux or MAC OS-X

Minimum of 8gb RAM (For human genome)

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