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Scripts for the analysis of low-coverage whole genome resequencing data

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whole-genome-reseq

Scripts and material for the processing and analysis of low-coverage individually-barcoded population genomes.

Note that some code modified from tsackton/ratite-genomics

Preprocessing

  1. rename_files_*.sh: readname raw sequencing read files for ease of use
  2. trim_fastq.sh: trim reads with Trimmomatic to remove adapter sequence

Map reads to assemblies

  1. make_bwa_index.sh: index assembly
  2. run_bwa_mem.sh: map reads to assembly, sort BAM, and dedup (submit_mapping_jobs.sh submits this script to SLURM for each read/assembly combination)
  3. merge_bams.sh: merge and second round dedup from BAM files produced by run_bwa_mem

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Scripts for the analysis of low-coverage whole genome resequencing data

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