1. Changed soft-linking of input fastq files to separate method, with explicit file matching
2. Added code to create new rawAlignment, processedAlignment, coverageTracks, and logs dirs when new analysis report dir is created.
3. Added code to remove split fastq bisulfite files after alignments have completed
4. Added a new field (column) for fastq file name in the Sample class to parse from the fresh data report
5. Fixed bug where output format wasn't specified as .sam for genomic sequences
6. Changed code to explicitly call filenames
7. Added code to Sample class to parse additional field for sequencing adapter from fresh data report
8. Added fields for SequenceLane, Read1Adapter, Read2Adapter, File(path)
Sample:
1. Added 4 new fields (w/ getters/setters) from autoalign report
2. Removed redundant, unused fields
Ketchup:
1. Fixed it so soft links are not followed or considered for file deletion
