April 26, 2016 at 1:59 am #1862
I tried to run novoalign today, but a block by an error that I do not know how to solve. The command and the error are shown as below.
./novoalign -d ~/Transcriptomes/dd_Smed_v6.pcf.contigs.inx -f ~/Omri_Single_Cell_RNAseq/SRR2051598.sra -o SAM -r Random > ~/Omri_Single_Cell_RNAseq/alignments.sam > ~/Omri_Single_Cell_RNAseq/log.txt
Stack Dump …
ip = 0x 4a10cf, sp = 0x 7ffe73244960
ip = 0x 409842, sp = 0x 7ffe73245130
ip = 0x 5de3e0, sp = 0x 7ffe73245140
ip = 0x 414c84, sp = 0x 7ffe73245580
ip = 0x 42eb5c, sp = 0x 7ffe732455b0
ip = 0x 42b11d, sp = 0x 7ffe73245740
ip = 0x 404093, sp = 0x 7ffe73245880
ip = 0x 5df5da, sp = 0x 7ffe73279d40
ip = 0x 409731, sp = 0x 7ffe73279e10
Please let me know if you have any thought or experience about this. Thanks for any help in advance.
April 26, 2016 at 2:30 am #1864
- This topic was modified 6 years, 2 months ago by email@example.com.
Novoalign can’t process an sra file. You need to extract the fastq file using
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