lh3: I will try BAQ right away to see if it improves things. Thanks for the advices
Unconfigured Ad
Collapse
X
-
Yeah, what I'm trying now and which seems to give very nice numbers of variants and ts/tv ratio is align->GATK realign/recalibrate(cleans up alignments)->BAQ->GATK Unified Genotyper(Dindel for indels). GATK's built-in filters are very nicely calibrated, at least in human.
Actually, Dindel is reporting more indels than I expect (a little under twice as many), but it could be that it's significantly more sensitive than samtools. But that's another thread.Mendelian Disorder: A blogshare of random useful information for general public consumption. [Blog]
Breakway: A Program to Identify Structural Variations in Genomic Data [Website] [Forum Post]
Projects: U87MG whole genome sequence [Website] [Paper]
Comment
-
-
If you're looking for aligners that find indels you could try the Omixon Variant Toolkit. It's a gapped aligner with spaced seeds similar to ShRIMP and BFast but it uses a different set of algorithms for the alignment. There's a cloud based web implementation (http://www.omixon.com/omixon/abouttoolkit.htm) where you can try it for free, and it's also available for free evaluation as a command line tool, you just need to send an email to [email protected].Originally posted by mathieu View PostHi epigen & John,
Thanks for your advices. I tried to install bioscope on our cluster but I gave up... Concerning BWA, it is the first one I tried and I was quite disappointed by the results since it has been highly recommended with low mapping rate (22.6%). The first results I have using BFAST and ShRIMP are almost the same in term mapping rate (57.5% and 51.2% respectively). However ShRIMP was a bit faster.
@epigen: For the SNP et InDels calling I am using samtools so far, but I am not very satisfied there are too many miscalls. What are your advices?
Comment
-
-
Hi Tim,Originally posted by Tim Hague View PostIf you're looking for aligners that find indels you could try the Omixon Variant Toolkit. It's a gapped aligner with spaced seeds similar to ShRIMP and BFast but it uses a different set of algorithms for the alignment. There's a cloud based web implementation (http://www.omixon.com/omixon/abouttoolkit.htm) where you can try it for free, and it's also available for free evaluation as a command line tool, you just need to send an email to [email protected].
This post is bordering on being too commercial for this forum...I'm going to let it stay here as it's relevant to the discussion but please just be aware in the future that overly commercial posts belong in the Vendor Forum. This was reported by a couple of people as too commercial.
Thanks!
-+Eric
Comment
-
-
Hi Eric,Originally posted by ECO View PostHi Tim,
This post is bordering on being too commercial for this forum...I'm going to let it stay here as it's relevant to the discussion but please just be aware in the future that overly commercial posts belong in the Vendor Forum. This was reported by a couple of people as too commercial.
Thanks!
-+Eric
Thanks for the friendly warning, I'm fairly new here and just learning the rules of the road! I wasn't trying to sell anything, just trying to help the OP with his issue.
Cheers,
Tim.
Comment
-
Latest Articles
Collapse
-
by SEQadmin2
Data variability is still an issue in sequencing technologies despite the advances in reproducibility and accuracy of these platforms. But the problem does not originate in the sequencing itself, but in the previous steps, before the sample reaches the sequencer.
The first step is collection, followed by preservation and sample preparation for analysis. Most scientists overlook those steps, but not being careful might just be skewing the experiment’s results.
...-
Channel: Articles
06-02-2026, 10:05 AM -
-
by SEQadmin2
With the launch of new single-cell sequencing platforms in 2026, the field stands at an exciting inflection point. This article surveys the most impactful advances in the field and discusses how they’re reshaping research in cancer, immunology, and beyond.
Introduction
Single-cell sequencing technologies have undergone remarkable advances over the past decade, transitioning from low-throughput experimental approaches to highly scalable platforms capable of...-
Channel: Articles
05-22-2026, 06:42 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Started by SEQadmin2, Yesterday, 10:09 AM
|
0 responses
10 views
0 reactions
|
Last Post
by SEQadmin2
Yesterday, 10:09 AM
|
||
|
Started by SEQadmin2, 06-04-2026, 08:59 AM
|
0 responses
19 views
0 reactions
|
Last Post
by SEQadmin2
06-04-2026, 08:59 AM
|
||
|
Started by SEQadmin2, 06-02-2026, 12:03 PM
|
0 responses
26 views
0 reactions
|
Last Post
by SEQadmin2
06-02-2026, 12:03 PM
|
||
|
Started by SEQadmin2, 06-02-2026, 11:40 AM
|
0 responses
21 views
0 reactions
|
Last Post
by SEQadmin2
06-02-2026, 11:40 AM
|
Comment