Unsupported: Use of this version of segemehl is not supported. More information on our Applications Support and Retention Policy.segemehl is a software to map short sequencer reads to reference genomes. Unlike other methods, segemehl is able to detect not only mismatches but also insertions and deletions. Furthermore, segemehl is not limited to a specific read length and is able to mapprimer- or polyadenylation contaminated reads correctly. segemehl implements a matching strategy based on enhanced suffix arrays (ESA). Segemehl now supports the SAM format, reads gziped queries to save both disk and memory space and allows bisulfite sequencing mapping and split read mapping.
Accessing segemehl 0.3.4-GCC-9.3.0
To load the module for segemehl 0.3.4-GCC-9.3.0 please use this command on the BEAR systems (BlueBEAR, BEAR Cloud VMs, and CaStLeS VMs):
module load bear-apps-unsupported/handbuilt/2019
module load segemehl/0.3.4-GCC-9.3.0
BEAR Apps Version
For more information visit the segemehl website.
Last modified on 27th May 2021