Update version in documentation
Add more verbose RNA-seq section to 0.7.0 changelog.
Merge pull request #72 from lbeltrame/doc-version-fix

Update version in documentation
Bug fix when concatenating multiple files and first is empty. Fixes #77. Provide ability to exclude samples from VCF files using GATK SelectVariants
Provide documentation on open file handles and tuning for scale. #60
Use new cloudbiolinux automated distribution detection for installation
Ensure we split galaxy *.loc files on only tabs, avoiding index errors when descriptions have spaces
Additional fixes for *.loc parsing using tool_data_table_conf: handle mixed spaces and tabs and fall back on remapping approaches correctly
Do not fail on non-GATC reference or variant bases. These will pass through unchanged without attempting to swap strands, but will no longer error out. Fixes #81
Avoid reading entire file when finding samples to exclude
Handle complements for multiallelic SNPs. Fixes #81
Handle simultaneous symlinking of results on distributed runs
Provide more useful error message with multiple jars in configured directory. Fixes #76
Merge branch 'master' of github.com:chapmanb/bcbio-nextgen
Correctly handle relative tool and data directory paths during installation. Fixes #82
Provide initial hooks to calculate coverage summary statistics for BAM files using bcbio.coverage. Provides a high level summary of coverage per genes of interest or all transcripts
Remove from ZeroMQ logging errors that silence logging
Ensure build parameter passed along to coverage assessment to allow contig remapping
Remove requirement for bcbio_system at the command line, detecting from automated install location if not specified. Improve documentation for getting started running the pipeline
Move whole genome example above exome since it runs directly without additional novoalign license