Short reads alignment failed

1. Get a huge sequence (e.g. NC_000067 from NCBI)
2. Copy small part of the sequence(~50) and create a set (~100k) of short reads from it, all reads should be equal
3. Align these short reads to reference sequence from step 1 using Bowtie
4. Wait and accept appeared import dialog
   Current state: UGENE can not open the result, logged error - [Can't decompress data]

Additional:

1. Move result sam file to another directory(without any additional files that appear during alignment)
2. Open it from UGENE
   Current state: import succeeded