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  • ewilbanks
    replied
    Any more ChIP-seq analysis tools that we should add here?

    Also, does anyone know if the program from the Poisson mixture method paper is publicly available?:


    Or if anything has been published about the ChIP-seq Analysis server?

    Leave a comment:


  • bioinfosm
    replied
    I think it will be a good idea to include RNA-SEQ tools in the huge table. The one tool I know for that = erange

    Leave a comment:


  • sparks
    replied
    Release V2.03.12 of Novoalign is out. This release improves performance especially for longer reads and is a 4-5 times faster on 45bp reads against Human. Longer reads have improved even more. Performance improvement is more pronounced when allowing more mismatches (higher thresholds).

    It also seems our web site has been blocked in China so if any one in China wants a copy of novoalign please email me at colin at novocraft dot com. I'll create a mailing list and keep you informed of any updates etc.

    Leave a comment:


  • Genomatix
    replied
    How about Genomatix?

    Hate to be so blatantly commercial, but in the "not for free" category, you should add Genomatix. No sales pitch here...but check out the vendor forum! Complete analysis capabilities for all current platforms...thanks.

    Leave a comment:


  • xuer
    replied
    RudyS,Thank you for the reply.for me the Installation if UCSC is finished, next i need to set the arabidopsis assembly. hopefully it goes well.

    Joann, Thank you for the information.The topics are interesting , i hope i could be there.

    Leave a comment:


  • Joann
    replied
    Meeting in Berlin this month

    Xuer, you might also access TAIR scientists who will be attending the International Biocuration Conference in Berlin later this month.
    Die EML European Media Laboratory GmbH ist ein Unternehmen, das forschungsnahe IT-Dienstleistungen von der Auftragsforschung über die Entwicklung innovativer IT-Lösungen bis hin zu Beratung und Schulung anbietet. Im Zentrum unserer Arbeit steht der Mensch: IT-Systeme sollen so entworfen und realisiert werden, dass ihre Benutzer sie als hilfreiche Erweiterungen ihrer eigenen Fähigkeiten erleben und nicht als technische Barrieren.

    Leave a comment:


  • RudyS
    replied
    xuer
    the browser is well documented ... suggest you write to the nice folks on the listserver there

    [email protected]

    Rudy

    Leave a comment:


  • xuer
    replied
    Originally posted by RudyS View Post
    thanks swbarnes2

    i think i will post a query on the UCSC listserver
    [email protected]
    and see if someone like Jim Kent is thinking about some utility that could facilitate reference assembly on a local Genome Browser ... he's the guy i think who initiated BLAT and isPCR on their site

    Explore, visualize, and compare genomic data with the UCSC Genome Browser: free, open-access tools for the human genome and beyond.


    the browser can be installed locally and used with any genome ... but without taking into account quality values from the reads its hard to imagine not getting just a mess doing a BLAT-like alignment ... i think

    RudyS
    Is there anybody have the experience to install UCSC locally with other genome database like arabidopsis? I hope I can find a detailed procedure to set it locally.
    Thanks!

    Leave a comment:


  • Batalov
    replied
    Originally posted by kopi-o View Post
    I didn't see MACS and PeakSeq among the ChIP-seq peak callers. Those should be added.
    Seconded. MACS is a useful tool.

    Leave a comment:


  • WJW-Davy
    replied
    MapView: a short reads alignment viewer with genetic variation analysis, visualization of short reads alignment on desktop computer

    Leave a comment:


  • xiechao
    replied
    CNV-seq

    a package to detect DNA copy number variation using shotgun sequencing.

    Leave a comment:


  • alig
    replied
    Consed is very similar to gap4 and now assembles illumina short reads.

    I have been happy with the assembly to a reference sequence & the contig viewer & searching for highly discrepant regions.

    hope this is of help

    alig

    Leave a comment:


  • polytoo
    replied
    Originally posted by rs705 View Post
    DNASTAR has changed the name of its integrated tool from SeqMan Genome Assembler to SeqMan NGen. it also works on Vista since that it what we are using with it.
    I would be interested to know how DNASTAR Seqman NGen does with ChIP-Seq as well as DGE alignments. I need to get data to complete neophytes off of all these platforms. Horsepower and speed could take back seat to "ease of use" since each user will be getting just a portion of a complete run.

    Any other packages that qualify as "easy to use" out there? Can any of them handle SRF files from a Helicos too?

    I know, not asking for much. Can it filter RAW and tie my shoes also?

    Leave a comment:


  • RudyS
    replied
    thanks swbarnes2

    i think i will post a query on the UCSC listserver
    [email protected]
    and see if someone like Jim Kent is thinking about some utility that could facilitate reference assembly on a local Genome Browser ... he's the guy i think who initiated BLAT and isPCR on their site

    Explore, visualize, and compare genomic data with the UCSC Genome Browser: free, open-access tools for the human genome and beyond.


    the browser can be installed locally and used with any genome ... but without taking into account quality values from the reads its hard to imagine not getting just a mess doing a BLAT-like alignment ... i think

    RudyS

    Leave a comment:


  • swbarnes2
    replied
    Originally posted by RudyS View Post
    swbarnes

    are you saying that there is some utility in the UCSC Genome Browser for assembling genomes from short reads? havent heard about that ...

    RudyS
    It's not assembly, it would be more like alignment, and I think I heard this is doable, but I don't work with any of the organisms they have there, so I didn't investigate for myself.

    Leave a comment:

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