Release 1.1.0

Bug-fixes and features:

• Mates mapped to different chromosomes are not checked for overlap
• Fasta IDs (reference genome) get truncated after first white space analogous to the behavior of most read mapping tools

Compatibility

• Interface and output format is fully compatible to v1.0.0

Release 1.0.0

This is the first release of RLM.

Features

• Support of BSMAP, BISMARK, segemehl and GEM aligners
• Support of WGBS, RRBS, amplicon and capture library stategies
• Calculation of PDR, RTS, entropy, epipolymorphism and single read statistics