Are there some research to Metagenomics using Solid???? Otherwise, the short read (about 50bp)to apply thie field????
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Thank you for your reply. I want to know whether some papers about Metagenomics on the basic of Solid sequencing.Originally posted by colindaven View PostAre you looking for software, or asking about whether people have used Solid in metagenomics so far ?
I think de novo assembly is a little trickier, but I'm not worried about the read length for our chosen analysis techniques.
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From the website
With a comprehensive portfolio of products, Applied Biosystems solutions from Thermo Fisher Scientific empower you to address today’s most pressing genetic challenges.
Metagenomics
Metatranscriptomic analyses of chlorophototrophs of a hot-spring microbial mat
Publication: The ISME Journal (2011)
Authors: Liu Z. et al.
Confirmation of the Sequence of 'Candidatus Liberibacter asiaticus' and Assessment of Microbial Diversity in Huanglongbing-Infected Citrus Phloem Using a Metagenomic Approach
Publication: Molecular Plant-Microbe Interactions, Vol. 22, No. 12, 2009
Authors: Tyler et al.
The carnivorous bladderwort (Utricularia, Lentibulaiceae) a system inflates
Publication: Journal of Experimental Botany, vol. 61, No1, pp 5-9, 2010
Authors: Albert, et al.
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In the NCBI SRA there are a couple more studies too, which may not be published:
1.
SOLiD sequencing of HLB infected Citrus phloem
1 ABI_SOLID (AB SOLiD System) run: 337.1M spots, 11.8G bases, 12.2GB downloads
Accession: SRX004995
CEG 50-50nt mate-pair library for sample GG3
1 ABI_SOLID (AB SOLiD System 3.0) run: 315.6M spots, 31.5G bases, 26.1GB downloads
Accession: SRX105134
25.
ABI 50-50nt mate-pair library for sample GG2
1 ABI_SOLID (AB SOLiD System 3.0) run: 281.8M spots, 27G bases, 22.3GB downloads
Accession: SRX105133
26.
ABI 75nt fragment library for sample GG1
2 ABI_SOLID (AB SOLiD System 3.0) runs: 339.8M spots, 25.5G bases, 20.7GB downloads
Accession: SRX105132
27.
CEG 35nt fragment library for sample GG1
1 ABI_SOLID (AB SOLiD System 2.0) run: 171.6M spots, 6G bases, 5.2GB downloads
Accession: SRX105131
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Thanks colindaven, neat papers, esp. genome-from-metagenome one. And yet I still have a question: is it even possible to use raw color-space reads (ie no assembly, no transforming to base space) to analyse a metagenome? As I've heard, BFAST and some other tools can do alignment of .csfasta against reference genome, but will they work against, say, NCBI database?
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by GATTACATLove this - good data definitely starts from good input, and poor input can only give relatively poor data. I particularly like the mention of Nanodrop/absorbance based methods for quantification. It's such a toss up if you'll get an accurate reading or what amounts to a randomly generated number, and a lot of library/sequencing related issues can be traced back to poor quant.
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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.
Here are nine questions we think about, in roughly the order they matter, before...-
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