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Thread | Thread Starter | Forum | Replies | Last Post |
MAnorm: a robust model for quantitative comparison of ChIP-Seq data sets | z3mao | Epigenetics | 0 | 03-20-2012 05:30 PM |
ChIP-Seq: MAnorm: a robust model for quantitative comparison of ChIP-Seq data sets. | Newsbot! | Literature Watch | 0 | 03-20-2012 03:20 AM |
Multiple Alignment of miRNAs with Precursors | polsum | Bioinformatics | 0 | 03-06-2012 10:47 AM |
Common elements within two set of miRNAs | Giorgio C | Bioinformatics | 1 | 01-05-2012 10:35 AM |
mapping reads to known miRNAs precursors | vebaev | Bioinformatics | 1 | 08-03-2011 06:48 AM |
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#1 |
Member
Location: ITALY Join Date: Oct 2010
Posts: 89
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Hi all,
i have two sets A and B of miRNAs. How i can make a comparison of them considering common elements and not ? Is there any tool that makes this type of comparison ? Thanks in advance for your help |
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#2 |
not just another member
Location: Belgium Join Date: Aug 2010
Posts: 264
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which type of data ? explain a little bit more about your problem
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#3 |
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Location: ITALY Join Date: Oct 2010
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There are two sets of miRNAs one coming out from a leaf and the other from the flower of the same Orchid. I have to know what are the differences between these two sets:
Elements in common and not. They are both in fasta format and in replicate (trimmed, filtered and collapsed with galaxy tools) originally coming out from a 454 platform. they apper like this: >1-8490 ACGTCACTCTCTCC.. >2-7990 CGTCAATCGCCTCC.. >3-6696 ACGTGCACTGCATG.. the first number is the Id , the second represents the number of occurences. I need to evidence what are the differences fromt he two sets. Do you have any advice ?? tnx |
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#4 |
not just another member
Location: Belgium Join Date: Aug 2010
Posts: 264
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Ok
First annotate your reads : align them against mirbase databse (with blats per example) and then count for each miR, the number of reads. After that in R create a matrix : each line represent one miR, each column a sample. Then use DESeq or edgeR for the DE analysis |
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#5 |
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Location: ITALY Join Date: Oct 2010
Posts: 89
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thank you very much for your fast reply. Is a problem that most of the miRNAs are novel and have no match with the database ??
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#6 |
not just another member
Location: Belgium Join Date: Aug 2010
Posts: 264
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maybe try miRDeep before DE analysis
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#7 |
Member
Location: ITALY Join Date: Oct 2010
Posts: 89
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Yes, i'v just done it with mirDeep but being this type of Orhichid not yet annotated i have a lot of no matching elements
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