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Thread | Thread Starter | Forum | Replies | Last Post |
Galaxy smallRNA Analysis help | smallSeq | Bioinformatics | 2 | 02-25-2016 04:55 PM |
smallRNA annotation | NicoBxl | Bioinformatics | 8 | 07-18-2012 10:11 AM |
smallRNA data | dnusol | Bioinformatics | 1 | 02-22-2011 12:38 AM |
SmallRNA analysis pipeline | naluru | SOLiD | 5 | 12-13-2010 12:59 AM |
multiplexing smallRNA | moguin | Illumina/Solexa | 7 | 09-16-2010 03:06 PM |
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#1 |
Member
Location: us Join Date: Apr 2016
Posts: 14
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Hello!
I am new to smallRNA seq and I am a bit confused as to analyze my data (from human genome). it is better to: 1) align against ncRNA transcriptome from Ensembl 2) align against genome 3) aling against miRNA transcript, take the unaligned reads, align them against genome and after that annotate them with gtf file. Or are there better options? Thank you in advance Best |
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#2 |
Member
Location: Santa Cruz, CA Join Date: Feb 2017
Posts: 17
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I found that when exploring new data CAP-miRSeq is really helpful:
http://bioinformaticstools.mayo.edu/...ch/cap-mirseq/ |
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smallrna |
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