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  • shurjo
    replied
    Originally posted by chadn737 View Post
    True, but 470K is a very small bam file, even for a small data set of only 1GB.
    Agreed. Maybe we will get a better insight after camelbbs looks at the actual BAM file to see what's in it.

    Another option would be to run FastQC on the input file to check the quality of the reads.

    Leave a comment:


  • chadn737
    replied
    Originally posted by shurjo
    This is absolutely normal. accepted_hits.bam is in the binary BAM format which uses much less space than fastq (which is in text format).
    True, but 470K is a very small bam file, even for a small data set of only 1GB.

    Leave a comment:


  • shurjo
    replied
    Originally posted by camelbbs View Post
    I am running tophat index/mm9 1.fastq

    to get accepted_hist.bam

    The running process has no error. But 1.fastq has 1Gb, accepted_hist.bam only has 470K.

    So What does it mean? It means only a few reads has mapped to reference genome?

    I downloaded mm9 from bowtie website and contructed a .fa file using bowtie-inspect mm9 > mm9.fa

    Anyone know this problem?

    thanks!
    This is absolutely normal. accepted_hits.bam is in the binary BAM format which uses much less space than fastq (which is in text format).

    Leave a comment:


  • camelbbs
    replied
    Originally posted by chadn737 View Post
    Did you check look at your alignment file to see if anything was aligned or check the tophat log files?
    Hi chadn737,

    May you recommend some good method to extract gene expression from RNA seq data.

    Now I am using tophat and cufflinks but the result seems not I want.

    BTW, does the reference genome mm9 I used is right?

    Leave a comment:


  • camelbbs
    replied
    thanks, I have checked my result , I really got some result but the result number is so small.

    Leave a comment:


  • chadn737
    replied
    Did you check look at your alignment file to see if anything was aligned or check the tophat log files?

    Leave a comment:


  • camelbbs
    replied
    I am curious why no people reply this? anyone can help?

    Leave a comment:


  • camelbbs
    started a topic question about tophat

    question about tophat

    I am running tophat index/mm9 1.fastq

    to get accepted_hist.bam

    The running process has no error. But 1.fastq has 1Gb, accepted_hist.bam only has 470K.

    So What does it mean? It means only a few reads has mapped to reference genome?

    I downloaded mm9 from bowtie website and contructed a .fa file using bowtie-inspect mm9 > mm9.fa

    Anyone know this problem?

    thanks!

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    New Genomics Technologies Take Aim at Long-Standing Limits
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