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Thread | Thread Starter | Forum | Replies | Last Post |
pipeline for ion torrent data | aituka | Bioinformatics | 11 | 05-21-2012 05:08 PM |
Ion Torrent data quality impressions? | rcorbett | Ion Torrent | 15 | 03-27-2012 12:43 PM |
Metatranscriptome analysis - MiSeq or Ion Torrent? | ramsemm | Ion Torrent | 5 | 03-06-2012 11:52 AM |
GATK and Ion Torrent data | NextGenSeb | Bioinformatics | 2 | 02-12-2012 09:36 PM |
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#1 |
Junior Member
Location: USA Join Date: Jul 2012
Posts: 8
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Hi everyone,
I wanted to start a thread to get an idea what other ion torrent users are using/doing for their downstream data analysis. There are a number of preferred software vendors suggested by ion torrent including DNASTAR, Avadis NGS, Partek and NextGENe. Has anyone used these and do you have any recommendations? I am in the process of trying a few of them out and wanted to hear what other people thought. I suppose whatever software you select depends on the type of work you are doing. I work in a microbiology lab so we will be doing some genome sequencing (so assemblies of genomes and alignments against a reference), RNA-seq (looking at transcript geography and expression levels) and possibly some ChIP-seq. I would be particularly interested to hear from other microbiologists who are doing similar work on the ion torrent but any feedback is welcome. Cheers, Ronan. |
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#2 |
Member
Location: Maryland Join Date: Aug 2011
Posts: 52
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https://learn.appliedbiosystems.com/...ctorsequencing
You can find Web-Based Training in the link above. Best wishes. |
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#3 |
Junior Member
Location: Edmonton, Canada Join Date: Aug 2012
Posts: 4
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I am trying to detect rare variants in pooled mutated samples. I have barcoded my pools and I have 3 genes I am analyzing in each of 28 pools. Since I am doing this as a test with diluted samples bearing a known mutation I can confirm if the technique is working. I can clearly see the expected mutations (around 2% change), but also see a bunch of sequencing errors, mainly at the end of the reads, which at the end show frequencies close to the real mutation. I been struggling for the last couple of days with SAMtools, CRISP and even the ion torrent variant call plugin without success (this lat one only calls alleles with a minimum of 5% frequency and rare mutations are lower than that. I know there are other Biologist-friendly tools out there, but they are usually expensive, so I am also on the lookout for something free and efficient.
I would mainly like to find a way to tell those sequencing errors from the real variants...any advise? |
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