breseq is a computational pipeline for finding mutations relative to a reference sequence in short-read DNA resequencing data. It is intended for haploid microbial genomes (<20 Mb). breseq is a command line tool implemented in C++ and R.
Implement in C++ and use R for some visualization.
[ ] Provide command line input functionality for linking together FASTQ files as containing paired reads. Probably connect them via an unusual character combination that is OK in the
shell and then split the argument, something like R1.fastq%R2.fastq
[ ] Add bowtie2 commands allowing mate-pair mapping. Be sure this does not interfere with split-read JC evidence steps.
[ ] Estimate the normal distribution of insert lengths and orientations from the data and generate QC graphs and output files.
[ ] Find consistent outliers and define as new MP evidence type.
[ ] Integrate MP evidence with predicting mutations: for example IS element insertions, deletions, and amplifications.
Implement in C++ and use R for some visualization.
R1.fastq%R2.fastq
bowtie2
commands allowing mate-pair mapping. Be sure this does not interfere with split-readJC
evidence steps.MP
evidence type.MP
evidence with predicting mutations: for example IS element insertions, deletions, and amplifications.