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?
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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
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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.
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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.
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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.
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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.
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xuer
the browser is well documented ... suggest you write to the nice folks on the listserver there
[email protected]
Rudy
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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.Originally posted by RudyS View Postthanks 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
Thanks!
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MapView: a short reads alignment viewer with genetic variation analysis, visualization of short reads alignment on desktop computer
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CNV-seq
a package to detect DNA copy number variation using shotgun sequencing.
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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
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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.Originally posted by rs705 View PostDNASTAR 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.
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?
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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
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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.Originally posted by RudyS View Postswbarnes
are you saying that there is some utility in the UCSC Genome Browser for assembling genomes from short reads? havent heard about that ...
RudyS
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I’m not a sequencing expert. I’m a purification scientist who uses NGS to evaluate workflows my group develops. With this perspective, we think about the sample first and the NGS workflow second. The sequencer is an exceptionally honest reporter, but it can only report on what you give it, so whether you get clean, interpretable data from an NGS workflow is largely determined before you begin.
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