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Thread | Thread Starter | Forum | Replies | Last Post |
how to identify number of fragments are produced for given gene in RNA-seq? | Muthukumar | RNA Sequencing | 4 | 03-11-2016 03:16 AM |
read number in fastq does not match bwa-mem produced sam file | melis | Bioinformatics | 0 | 09-29-2015 10:39 AM |
Adding counting Contig number at the start of Fasta Sequences | Zapages | Bioinformatics | 3 | 05-12-2015 09:03 AM |
Easiest way to get number of reads per contig? | kmkocot | Bioinformatics | 2 | 05-14-2013 04:53 PM |
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#1 |
Junior Member
Location: Tehran Join Date: Jan 2017
Posts: 3
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i have 11700000 paired end reads.when i run denovo assembly by Genious , 130000 contig is produced. can i help me to in this issue?????
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#2 |
Senior Member
Location: East Coast USA Join Date: Feb 2008
Posts: 6,698
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Your best bet is to contact Geneious tech support. Your question is very generic and you are using a commercial software package which is going to make it difficult to get useful help here.
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#3 |
Senior Member
Location: US Join Date: Dec 2010
Posts: 323
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Anybody looking at this would need some more info: What type of organism? Which genome size is expected? What read lengths did you use? What library prep protocol and insert sizes?
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#4 |
Member
Location: Germany Join Date: Oct 2016
Posts: 10
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Given the fact that issues can occur anywhere beginning from samplequality,library-preparation, sequencing and last but not least parameter-settings used for assembly, it is hard to provide help with this minimum amount of information. But probably the first, cost and time effective thing you could try is to test a range of different kmer-sizes and keeping track of the changes in N50. Another thing you could check if your genome is diluted by very short sequence clusters (nearly readlength). Maybe throwing away all contigs <200bp still represents 99% of your target genome and you will end up with much less contigs in total.
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