[2018-05-11 13:20:10] Beginning TopHat run (v2.1.1)
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[2018-05-11 13:20:10] Checking for Bowtie
		  Bowtie version:	 2.2.2.0
[2018-05-11 13:20:10] Checking for Bowtie index files (genome)..
[2018-05-11 13:20:10] Checking for reference FASTA file
[2018-05-11 13:20:10] Generating SAM header for Bowtie2Index/genome
[2018-05-11 13:20:12] Reading known junctions from GTF file
[2018-05-11 13:20:15] Preparing reads
	 left reads: min. length=33, max. length=33, 17260311 kept reads (8047 discarded)
[2018-05-11 13:22:43] Building transcriptome data files /scratch/6177259.1.p16/tophat2/tmp/RefSeq_GeneBody
[2018-05-11 13:22:52] Building Bowtie index from RefSeq_GeneBody.fa
[2018-05-11 13:27:46] Mapping left_kept_reads to transcriptome RefSeq_GeneBody with Bowtie2 
[2018-05-11 13:31:02] Resuming TopHat pipeline with unmapped reads
Warning: you have only one segment per read.
	If the read length is greater than or equal to 45bp,
	we strongly recommend that you decrease --segment-length to about half the read length because TopHat will work better with multiple segments
[2018-05-11 13:31:02] Mapping left_kept_reads.m2g_um to genome genome with Bowtie2 
[2018-05-11 13:32:33] Searching for junctions via segment mapping
[2018-05-11 13:33:36] Retrieving sequences for splices
[2018-05-11 13:34:42] Indexing splices
Building a SMALL index
[2018-05-11 13:34:53] Mapping left_kept_reads.m2g_um_unmapped to genome segment_juncs with Bowtie2 (1/1)
[2018-05-11 13:34:54] Joining segment hits
[2018-05-11 13:38:25] Reporting output tracks
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[2018-05-11 13:42:30] A summary of the alignment counts can be found in /scratch/6177259.1.p16/tophat2/align_summary.txt
[2018-05-11 13:42:30] Run complete: 00:22:19 elapsed
[samopen] SAM header is present: 22 sequences.
[bam_sort_core] merging from 4 files...