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10.0 years ago
k.solaymane
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0
Hi all, we have sequenced the whole genome of pooled organisms, we have a data set from illumina hi seq with matepair library 8kb in insert sequenced 2X100, I look for bioinformatic tool to cluster my reads within organisms etc... any suggestion ... Thank you!
Hi mikhail, so we have pooled our bacteria at ratio 1OD:1OD... then we performed a unique genomic DNA extraction followed by sequencing.. Thank you
If you are working with known samples and have them barcoded (http://www.illumina.com/technology/multiplexing_sequencing_assay.ilmn), then you'll need to de-multiplex them. In general the instrument (e.g. Illumina MiSeq) is capable of de-multiplexing itself. Then you can proceed with each of the samples separately. Otherwise I believe that you'll have to to apply some de-novo assembling strategy that accounts for multiple organisms present.
we haven't tagged our organisms, we have reads from the whole genomes . we want to look for % of the presence of each organism through reads..thank you for your intercation
Ok then MetAMOS is the option. Good luck!