Hello,
I am working on SOLiD RNA-seq data. I would like to find chimeric transcripts or fusion genes discovery with this data. But, the softwares, which does fusion genes discovery were written for FASTQ format files.
So, I tried converting my color space files to fastq by solid2fastq in BFAST and MAQ and the fusion genes discovery with the resulting files was a disaster as the conversion of .csfasta files to FASTQ is not straightforward as described in BFAST and MAQ
I thought I can convert the mapped colorspace reads to FASTQ files and use those softwares.
Is there a way to get the mapped reads and unmapped reads from TOPHAT? or any other alternatives to solve my problem?
Any help in this regard will be greatly appreciated.
Thanks,
I am working on SOLiD RNA-seq data. I would like to find chimeric transcripts or fusion genes discovery with this data. But, the softwares, which does fusion genes discovery were written for FASTQ format files.
So, I tried converting my color space files to fastq by solid2fastq in BFAST and MAQ and the fusion genes discovery with the resulting files was a disaster as the conversion of .csfasta files to FASTQ is not straightforward as described in BFAST and MAQ
I thought I can convert the mapped colorspace reads to FASTQ files and use those softwares.
Is there a way to get the mapped reads and unmapped reads from TOPHAT? or any other alternatives to solve my problem?
Any help in this regard will be greatly appreciated.
Thanks,
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