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Thread | Thread Starter | Forum | Replies | Last Post |
GATK with non-model organism (Help with making SNP VCF file)) | newbietonextgen | Bioinformatics | 7 | 09-10-2012 08:59 AM |
Cufflinks non-model organism, issues with -b, and false concatenation of genes | waspboyz | Bioinformatics | 3 | 06-20-2012 08:01 AM |
Finding Exon-Intron Junctions without a reference genome | brachysclereid | Bioinformatics | 3 | 05-22-2011 07:21 AM |
Methods for 'exploratory analysis' of sequenced non-model organism transcriptomes | ShellfishGene | Bioinformatics | 2 | 11-16-2010 09:38 AM |
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#1 | |
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Location: USA Join Date: Sep 2012
Posts: 41
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I desperately need some help in brainstorming how to approach my data. I have a de novo assembled genome of a non-model organism (no available reference genome) and my end goal is to annotate it and find the genes that determine/play a role in sex development. I plan to map/align the assembly to a related species that has an annotated reference genome. The data was sequenced pair end by illumina hiseq.
I am stuck on what to do next, what would be a suggested pipeline on how to go about finding the genes of interest? And what programs/software open source or commercial can I use to achieve that? How do I go about annotating it? A related post I posted some few weeks ago is below, no responses yet ![]() Please, any ideas/suggestions or directions to an already similar answered post are welcomed. Thank you very much. Quote:
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#2 |
Senior Member
Location: sub-surface moon base Join Date: Apr 2013
Posts: 372
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Predict proteins with FragGeneScan. Blastp against nr. Predict tRNAs with tRNAscan-SE. Predict rRNAs with Blastn against silva SSU and LSURef?
Alternatively, you could consider just submitting your data to IMG (if it's suitable for your organism) and let them do the computations for you? You could at least have a look at their SOP for ideas? Last edited by rhinoceros; 01-23-2014 at 10:49 AM. |
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#3 |
Senior Member
Location: Adelaide, Australia Join Date: Sep 2010
Posts: 119
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It completely depends on your species/sequence.
How big is your genome? Is it repetitive? How close (taxonomically) is the nearest well-annotated genome? Have you outlined functional gene families that you want to target? Best bet is to identify ORFs with a gene finder (FGENESH, Augustus, GENSCAN), extract sequences and BLAST against a well-annotated gene/protein db of a closely related species... |
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#4 |
Senior Member
Location: Woodbridge CT Join Date: Oct 2008
Posts: 231
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Is this an organism possessing a phenotypic male and female organism in it's reproductive cycle or does it have a more obscure developmental strategy?
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#5 |
Member
Location: USA Join Date: Sep 2012
Posts: 41
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#6 | |
Senior Member
Location: Halifax, Nova Scotia Join Date: Mar 2009
Posts: 381
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Find contigs with ORFs, and then run these through BLAST2GO. You can then filter the annotations based on E-value |
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#7 |
Junior Member
Location: Norway Join Date: Sep 2012
Posts: 3
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Would like to just follow up on this post a little bit. Is it possible to get some faster annotation than by Blast2GO for non-model organisms? For me at least the blast step is running very slow (meaning weeks), even if using a more powerful computer. Does it help a lot to get a local BLAST database?? Or anyone has experience with the new Blast2GO CLC plugin, does it run faster? Thanks in advance!! :-)
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#8 | |
Member
Location: Guangzhou China Join Date: Aug 2013
Posts: 82
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Tags |
annotation, de novo genome, illumina hiseq 2000 reads, non-model organism, pipeline |
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