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  • EMeyer
    replied
    Mark,

    I know its not what you were asking for in this post, but if a set of 454 reads (~600k raw reads) would be useful for testing Euler-SR, I'd be happy to share those with you in exchange for a quick explanation of the output from this program

    Leave a comment:


  • lh3
    replied
    This is what Clive was talking about:

    ftp://ftp.ncbi.nih.gov/pub/TraceDB/ShortRead/SRA000271/

    40X human resequencing. All PE reads. They have been there for a month or so. (Sorry, not for bacteria...)

    Leave a comment:


  • Torst
    replied
    The NCBI short read archive might have some.



    It certainly has some 454 FLX (paired) data, and some "Illumina GA" data for Bacteria, but unclear if it is paired.

    Leave a comment:


  • mchaisso
    replied
    ... more clarification ...
    ideally bacterial or small fungal genomes. I'm working on de novo assembly, and my code isn't mature enough to handle the complicated mammalian repeat structure.
    Last edited by mchaisso; 07-06-2008, 09:55 PM.

    Leave a comment:


  • cgb
    replied
    theres about 300GB of paired end illumina data at NCBI - all Human.

    Leave a comment:


  • mchaisso
    replied
    Originally posted by ScottC View Post
    How about the K12 genome from CLC. It's provided for evaluation of their Genomics Workbench. They have Illumina (E. coli K12), ABI (S. suis) and Roche (E. coli K12) data sets. Click the link below saying "Alternatively, you can download the raw data here".

    http://www.clcbio.com/index.php?id=1290
    Thanks for the link... they are an interesting company.

    I should mention that I'm looking for anything but K12.

    Leave a comment:


  • ScottC
    replied
    How about the K12 genome from CLC. It's provided for evaluation of their Genomics Workbench. They have Illumina (E. coli K12), ABI (S. suis) and Roche (E. coli K12) data sets. Click the link below saying "Alternatively, you can download the raw data here".

    Welcome to QIAGEN Digital Insights LabCorp uses QCI and HGMD to improve identification and interpretation of genetic variants within inhereited diseases.Read...

    Leave a comment:


  • mchaisso
    started a topic Paired-end Illumina data

    Paired-end Illumina data

    Does any body have paired end illumina data they are willing to share for the purposes of testing euler-sr? I'd prefer bacterial genomes, and am willing to sign any required non-disclosure agreements.

    Thanks,
    -mark

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