Hello,
I am trying to align Solid reads that map uniquely to the C. Elegans genome. I have a fastq file that has 4 lines for each read that are 50 bases in length. The reads are in color space (0-3). I have very little programming experience outside of writing simple perl scripts and am very new to next generation sequencing.
I have successfully used bowtie in the past to align reads to the human genome from Solexa data, but for some reason, I am having difficulty getting started with the latest version of BFAST. I have been reading the manual for a couple hours, which seems straightforward, but I think that there are some installation steps that I need to execute before creating the index and matching the reads.
I am working on a linux system. Could someone please tell me the commands that I need to enter to install BFAST? I entered the command, ./configure and got a response, but I think there are some additional steps that remain for the installation process.
Thanks,
cutcopy11
I am trying to align Solid reads that map uniquely to the C. Elegans genome. I have a fastq file that has 4 lines for each read that are 50 bases in length. The reads are in color space (0-3). I have very little programming experience outside of writing simple perl scripts and am very new to next generation sequencing.
I have successfully used bowtie in the past to align reads to the human genome from Solexa data, but for some reason, I am having difficulty getting started with the latest version of BFAST. I have been reading the manual for a couple hours, which seems straightforward, but I think that there are some installation steps that I need to execute before creating the index and matching the reads.
I am working on a linux system. Could someone please tell me the commands that I need to enter to install BFAST? I entered the command, ./configure and got a response, but I think there are some additional steps that remain for the installation process.
Thanks,
cutcopy11
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