Jing
All good thoughts and if I remember correctly, custom software can indeed to incorparated into Galaxy through use of the "Toolshed" . I'll check into this with Jennifer.
Thanks
Scott
Scott Tighe Senior Core Laboratory Research Staff Advanced Genome Technologies Core University of Vermont Vermont Cancer Center 149 Beaumont ave Health Science Research Facility 303/305 Burlington Vermont 05405 802-656-2557
On 10/6/2013 9:59 AM, Jing Yu wrote:
Dear Scott,
I think what you propose is doable.
You may
- use a 16s or gyrase DNA sequence as feeds to blast against your
data to get the relative sequences, 2. and then use the sequences as feeds to blast against your nucleotide database with appropriate filters.
There are several ways to make the steps. For example, you may already have the 16s sequence from assembly against a reference genome. And for Step 2, if you are not blasting thousands of times a day, and believe in the recent stability of NCBI, then a simple web_blast code will do the trick. Otherwise, since the local blast+ toolkit doesn't provide the equivalent organism filters, you'll have to work a wit bit on it:
Make a nucleotide database for Prokaryotes. Search txid561[ORGN] on http://www.ncbi.nlm.nih.gov/nuccore (this is for Escherichia as an example), Send to 'File' -> Format ->GI List When Blast, use this GI list as the value of this argument: -negative_gilist Then parse the Blast result.
Most of these can be automated with some code, but I don't know how to incorporate it into Galaxy.
Regards, Jing On 4 Oct 2013, at 23:52, Scott Tighe <scott.tighe@uvm.edu mailto:scott.tighe@uvm.edu> wrote:
Dear Jing
What you have outlined below is perfect.
I wonder how hard it would be to design a few filters that only look a certain genes and or filter model organisms out of the dataset.
For example, say you want only data for 16s or only gyrase, but no /E.coli/ and no /Pseudomanas aeroginosa/
Scott Scott Tighe Senior Core Laboratory Research Staff Advanced Genome Technologies Core University of Vermont Vermont Cancer Center 149 Beaumont ave Health Science Research Facility 303/305 Burlington Vermont 05405 802-656-2557 On 9/25/2013 12:06 AM, Jing Yu wrote:
Hi Scott,
My first thought is:
- Remove rDNA sequences (and/or other well known highly-conserved
sequences to reduce the workload in step 2). 2. Blast, then remove sequences with > (say 99%) match to > (say 5) genus. (Optional if step 1 is already good enough)
For step 1: Build a fasta file of the chosen highly conserved sequences, and use it as a feed to blast against your MiSeq result. Remove positive hits. For step 2: Blast remaining MiSeq sequences against NCBI (or whatever) database. Remove if it hits more than n genus.
Jing On 24 Sep 2013, at 22:17, Scott Tighe <scott.tighe@uvm.edu mailto:scott.tighe@uvm.edu> wrote:
Jing et al
Thank you for the offer to write some code to help advance the metagenomics arena. It is certainly needed.
So the problem is well known with megablast and shotgun metagenomics and without proper understanding and correct software will yield very misleading and in many cases incorrect data. For those of us who wish NOT to move to a protein level of comparison for specific reasons, we are stuck.
*The Problem:*
If I megablast 50 million sequences from a HiSeq run, millions of rRNA sequences will have a 99% match to all microbes rRNA genbank deposits. Not surprizing since the rRNA is highly conserved. The difference between E.coli and Shigella is 1 to 2 bases for the full 1540 bp 16s. So 16s is not useful for Genus level, and certainly not Species
*So what happens:*
The returned matches will have many hits to whatever model organism is in Genbank. For example E coli has 13000 entries for rRNA and Sphearotilus has 3 entries for rRNA. If the blasted sequence matches both, the results will mislead the investigator to think they have 13000 hits to E coli, EVEN if the microbe is Sphearotilus.
*The cure?:*
If there was a way to filter/ remove all hits ? Let say, for example, that a result has a first match (say E. coli) at >99% a second match (say Pseudomanas) at >99% and a third , forth and fifth match >99 for three other organisms. This sequence _must_ be discarded because it is a conserve sequence.
Basically conserved sequence is the enemy and invalidates the entire result.
**Another problem:*
If you have a reference sample with 19 non-model microbes, and you run that by HiSeq Shotgun for metagenomics and then megablast, what do you think you get? If E coli is not in the reference sample, how many hits do you think you get? Yes, 10,000 of thousands. So without removing conserved sequences, your data is wrong and you are much better served by culturing and running a Biolog metabolic panel and comparing to the sequence result.
So where do we start? I have some shotgun metagenomics data from the reference sample which included the 19 microbes. That was data from a MiSeq.
Scott Scott Tighe Senior Core Laboratory Research Staff Advanced Genome Technologies Core University of Vermont Vermont Cancer Center 149 Beaumont ave Health Science Research Facility 303/305 Burlington Vermont 05405 802-656-2557 On 9/20/2013 9:17 PM, Jing Yu wrote:
Hi Scott,
I can do some perl programming, such as local/remote blasting. Can you specify your problem a little bit clearer, so that maybe I can write a program to do just that?
Regards, Jing
Gerald
16s is basically useless for identification to genus. Since I started sequencing 16s in 1992, I have come to realize that without sequencing the full 1540 bases, it is generally misleading, and even than, it is not accurate enough to nail genus on more than 1/2 the cases. However, what is your feeling on ITS and gyrase, They seem to be far more discriminating but those databases have been decommissioned sometime ago.
The desirable thing would be that Galaxy or NCBI add a "filter conserved genes" [ ie any hit with a second choice greater than 3% distance]. Something such as that.
If you (or others) are aware of such a thing, I'd love the here about it.
Sincerely Scott