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HI All
How can I normalize differential Expression (log2) values from Cuffdiffs. I dont have replicate and am not good in unix based systems
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miRanalyzer standalone download
Hi,
I am trying to install miRanalyzer stand alone version. I have built the database and managed to download all required tools and packages. When I tried to run it with the test data provided, I get this message: "Failed to load Main-Class manifest attribute from miRanalyzer.jar
". Just wondering what I am doing wrong
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Solid is currently only supported through bowtie's (0.12.X) support for colorspace
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RPKM-normalization
Please, how do to normalize the data from SOLiD? I'll do differential expression. RPKM is the standardization? What does that mean exactly
thanks
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Hi Warren,
ERANGE currently assumes a fixed read length & isn't particularly mixed read-length friendly. It's a topic that's been on my mind a lot lately and I plan on fixing it.
Some of these problems relate to read-length in a direct way.
When reads are less than 32bp long, few enough reads cross-splices that we need the splice-junctions explicitly in order to recover the known splices (notice that the TopHat developers are very happy to recover 80% of the known splices that ERANGE sees) and de novo splice discovery has a very high false-positive rate.
As reads get in the 40-75 bp range, you can now map novel splices with some good confidence.
But as reads get longer, an increasing fraction of reads cross more than one splice.... one of the upcoming versions of ERANGE will deal with that.
If your reads are long enough, then ERANGE now supports a splice-junction free way of mapping splices (which is described in the ERANGE README.build-rds help file). Essentially, just map the reads on the regular genome with bowtie, explicitly saving the unmapped reads in a separate file. Then map those reads with blat (yes, it's slow) and only import those that map well onto the genome & that have an intron.
Ali
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Originally posted by alim View PostHi Warren,
I'm sorry if I didn't get back to you by email!
I certainly don't have any explicit support for SOLiD colorspace; since we only have Illumina sequencers at Caltech, I don't even have the data and tools to support it even if I wished.
But, assuming that you could dump the reads out of colorspace into fasta/fastq, then you should be able to map the reads against a reference genome (or reference+splice junction, aka an "expanded genome") using bowtie and then proceed with the rest of ERANGE !
There are several other packages out there that are just starting to appear. TopHat is another one that has support for RPKM, etc.... As far as I know, it also needs a reference genome & start from fasta/fastq.
Ali
Thanks for the response. I have checked out TopHat which also looks like quite an interesting package. I was wondering as well about using something like 454 with ERANGE since the read lengths vary can it still be used with the ERANGE package? I am specifically concerned about the creation of splice-reads and what value to select for the splice radius, if you have any thoughts please let me know.
Thanks again!
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ERANGE for non-Illumina data
Hi Warren,
I'm sorry if I didn't get back to you by email!
I certainly don't have any explicit support for SOLiD colorspace; since we only have Illumina sequencers at Caltech, I don't even have the data and tools to support it even if I wished.
But, assuming that you could dump the reads out of colorspace into fasta/fastq, then you should be able to map the reads against a reference genome (or reference+splice junction, aka an "expanded genome") using bowtie and then proceed with the rest of ERANGE !
There are several other packages out there that are just starting to appear. TopHat is another one that has support for RPKM, etc.... As far as I know, it also needs a reference genome & start from fasta/fastq.
Ali
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Originally posted by rs705 View PostCan you be a little more specific about what you want to do with RNA-Seq? There are a couple of software packages that are available, depending on what your interests are.
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Can you be a little more specific about what you want to do with RNA-Seq? There are a couple of software packages that are available, depending on what your interests are.
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ERANGE and other packages for RNAseq analysis
Hi everyone,
I am currently exploring the ERANGE package and was wondering whether there are other available packages like this to identify new regions and calculate statistics based on read counts.
Secondly, can this be applied to sequencing technologies other than Illumina? I havent recieved a reply from the authors so I figured I would ask the forum I was thinking of using SOLiD data which is roughly the same length as the illumina reads. Out of interest has anyone tried to use the package with other technologies?
Latest Articles
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by seqadmin
Non-coding RNAs (ncRNAs) do not code for proteins but play important roles in numerous cellular processes including gene silencing, developmental pathways, and more. There are numerous types including microRNA (miRNA), long ncRNA (lncRNA), circular RNA (circRNA), and more. In this article, we discuss innovative ncRNA research and explore recent technological advancements that improve the study of ncRNAs.
Nobel Prize for MicroRNA Discovery
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10-07-2024, 08:07 AM -
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by seqadmin
Metagenomics has improved the way researchers study microorganisms across diverse environments. Historically, studying microorganisms relied on culturing them in the lab, a method that limits the investigation of many species since most are unculturable1. Metagenomics overcomes these issues by allowing the study of microorganisms regardless of their ability to be cultured or the environments they inhabit. Over time, the field has evolved, especially with the advent...-
Channel: Articles
09-23-2024, 06:35 AM -
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