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Variant Incorporation Iterative Gap Filling

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VIIGF

Alan E. Yocca aeyap42@gmail.com @Aeyocca (twitter) Uploaded 03-27-19

This is a horrible acronym but it keeps the file names nice and concise

Built for use on University's cluster. Compatible with SLURM submission system

  • PBJelly part is still untested, working on that

Inputs:

  • Illumina paired-end reads

  • Reference genome

  • Run just the viigf_var_inc step to get a consensus genome from incorporating SNPs into the reference genome

  • I found marginal improvement after 3 rounds

    • test your own though, compare number of variants that still exist after 3 rounds

Configuration file:

  • set variables to what you need them to be
  • example configuration file: viigf_config_ragoo.conf

To set it all off!

  • make sure the configuration file is set how you would like it to be set
  • make sure reads are in either 01_raw_reads/ within ${WKDIR} or 04_trimmed
    • depending if they are trimmed reads or not
  • run ./viigf_launch.sh
    • type: $ ./viigf_launch.sh without any arguments to see the command line options

viigf_pbj.sbatch

  • untested as of 03-27-19
  • additionally, code written to run MaSuRCA, prefer other assembly methods though
    • since my MaSuRCA build is fragile

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