Dear all,
The last two months I have been fighting with MapSplice2.
First, we had troubles building the index, but this we fixed. But now, it throws an error regarding the fastqs.
python MapSplice-v2.2.0/mapsplice.py -c human/ensembl/bowtie_index/fasta -x bowtie_index/built_bowtie_index -1 <(zcat R1.fastq.gz) -2 <(zcat R2.fastq.gz) -p 3 -o output
-----------------------------------------------
[Thu Feb 25 09:20:28 2016] Beginning Mapsplice run (MapSplice v2.2.0)
[Thu Feb 25 09:20:28 2016] Bin directory: MapSplice-v2.2.0/bin/
[Thu Feb 25 09:20:28 2016] Preparing output location
[Thu Feb 25 09:20:29 2016] Checking files or directory: /dev/fd/63
[Thu Feb 25 09:20:29 2016] Checking files or directory: /dev/fd/62
[Thu Feb 25 09:20:29 2016] Checking files or directory: /data/human/ensembl/bowtie_index/fasta/
[Thu Feb 25 09:20:29 2016] Checking Bowtie index files
[Thu Feb 25 09:20:29 2016] Inspecting Bowtie index files
[Thu Feb 25 09:20:31 2016] Checking reference sequence length
[Thu Feb 25 09:20:44 2016] Checking consistency of Bowtie index and reference sequence
[Thu Feb 25 09:20:44 2016] Checking read format
-----[Read Format: FASTQ]
-----[Read Type: Pair End]
Base name of two ends not consistent
The 1th read in /dev/fd/63 and /dev/fd/62
FHIIIGI?FAEBFHGGGGGGHEHEEEEECCCCBCBBBBBBBBBB
@HS12_346:7:1101:1516:1746/2 2:N:0:TCGGCA
[MapSplice Running Failed]
Error: Checking read format failed
I do not understand what the problem is. The files work fine with other fusion gene finding tools.
Thanks for any help!
- Ninni
The last two months I have been fighting with MapSplice2.
First, we had troubles building the index, but this we fixed. But now, it throws an error regarding the fastqs.
python MapSplice-v2.2.0/mapsplice.py -c human/ensembl/bowtie_index/fasta -x bowtie_index/built_bowtie_index -1 <(zcat R1.fastq.gz) -2 <(zcat R2.fastq.gz) -p 3 -o output
-----------------------------------------------
[Thu Feb 25 09:20:28 2016] Beginning Mapsplice run (MapSplice v2.2.0)
[Thu Feb 25 09:20:28 2016] Bin directory: MapSplice-v2.2.0/bin/
[Thu Feb 25 09:20:28 2016] Preparing output location
[Thu Feb 25 09:20:29 2016] Checking files or directory: /dev/fd/63
[Thu Feb 25 09:20:29 2016] Checking files or directory: /dev/fd/62
[Thu Feb 25 09:20:29 2016] Checking files or directory: /data/human/ensembl/bowtie_index/fasta/
[Thu Feb 25 09:20:29 2016] Checking Bowtie index files
[Thu Feb 25 09:20:29 2016] Inspecting Bowtie index files
[Thu Feb 25 09:20:31 2016] Checking reference sequence length
[Thu Feb 25 09:20:44 2016] Checking consistency of Bowtie index and reference sequence
[Thu Feb 25 09:20:44 2016] Checking read format
-----[Read Format: FASTQ]
-----[Read Type: Pair End]
Base name of two ends not consistent
The 1th read in /dev/fd/63 and /dev/fd/62
FHIIIGI?FAEBFHGGGGGGHEHEEEEECCCCBCBBBBBBBBBB
@HS12_346:7:1101:1516:1746/2 2:N:0:TCGGCA
[MapSplice Running Failed]
Error: Checking read format failed
I do not understand what the problem is. The files work fine with other fusion gene finding tools.
Thanks for any help!
- Ninni
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