Exome Sequencing

[ketan_bnf]

Hi!

I am also working on Exome annotation. I have 454 sequencing data, so i am planning to use MOSAIK for aligning reads to ref. chromosome and then extract data from aligned_sorted file to BAM/SAM format, going to analyze with samtools.

Is this the right pipeline for Exome annotation SNP finding of 454 data?
Does bwa supports long reads (>=200) of 454 seq data? can it handle that?

Thanks,

[bioinfosm]

hey thats great!

From bedtools "New "per base depth feature" (-d) added to coverageBed. This reports the per base coverage (1-based) of each feature in file B based on the coverage of features found in file A. For example, this could report the per-base depth of sequencing reads (-a) across each capture target (-b). "

Guess will have to try it out to see what it really looks like!

[hrajasim]

Estimating breadth and depth of coverage

AFter trying a couple different approaches, I concluded that using the coverageBed script in BEDTools is the easiest way to determine the breadth and depth of coverage.

coverageBed -abam reads.bam b exons.bed -hist >result.txt

When the run completes, you need to look at the end of the result.txt file for the 2 column data to plot the histogram.

[nhansen]

This information is easy to get using samtools on a BAM file produced by any decent aligner (like bwa). The "samtools mpileup" function will report the number of reads covering each reference position (depth), and you can simply use awk and bed tools to generate your metrics.

I would caution you against using a minimum of 1 base coverage as your metric for coverage. For diploid sequences, one read is completely useless. For coverage, we count bases at which we can call a genotype with >99.9% confidence. This usually works out to be somewhere in the 10-20x range, depending on the bases seen.

Hope that helps!
--Nancy

[hrajasim]

I am trying to understand the exome-capture dataset we got for human and mouse (separate projects). To begin with, I am interested in estimating:

1. How much of the exome is covered by at least 1 (or N) base(s). (breadth of exome coverage)
2. What is the depth at which each exon is covered. (Depth of exome coverage)

Anybody has done this kind of analysis?
Please suggest if there are tools that I could use for this purpose.
Harsha

[NGSfan]

regarding "out of target" sequence freebies... becareful with pseudogenes and paralogs... the capture kits will pull down things that can cross-hybridize with your baits

this can also mess up your intended targets...

anyone come up with a way to handle these in an automatic fashion? to ignore genes affected by pseudogenes / paralogs?

[bioinfosm]

We see some decent coverage in non-target regions. Has anyone looked at that? Probably its good data, when one sees more than 10x coverage of coding regions, even when not targeted by the capture kit. However, they could certainly be false!

@jeckow, whats your experience with annovar, could you comment on its usage, time to run, efficiency, etc..

[Jeckow]

Align with bwa.

Then i suggest you to use GATK. You can analyse multiple samples at once and it gives a robust set of calls and allows for a whole-exome specific pipeline..Cool!

Once GATK analysis is completed, you can annotate called variations by annovar.

That's all!

[bpetersen]

I am also currently trying to find out the best way to handle exome sequencing data (sureselect, sequenced on the solid).
It seems to me, that most people map against the whole genome, not an exome sequence, probably to reduce false positive SNPs in the end. So my plan for a pipeline looks like this so far:

1. Align against whole genome (with bioscope in my case)
2. remove duplicates with picard
3. SNP calling with bioscope, as well as samtools pileup (to compare results)
4. filter out the SNPs in the targeted region

So far I'm not quite sure, of the best way to filter in the last step. I'd be very grateful for some suggestions. :-)

[zee]

For SNPs and Indels do try Novoalign as it performs quite well in terms of accuracy but is slower than BWA.

We also have a Novoalign NGS guide doing this basic variant detection pipeline.

Basically

1. Align with novoalign
2. Sort alignments
3. Merge if you have multiple runs for the same library
4. Remove PCR duplicates with samtools or Picard
5. Run the samtools pileup variation caller
6. Filter

See the posted link for command line examples

[svl]

One possibility:
1. align with BWA
2. get variation with SAMTOOLS pileup

http://bio-bwa.sourceforge.net/

http://samtools.sourceforge.net/cns0.shtml

[Shruti Madhiwalla]

I am looking for snps in the data.

[NGSfan]

can anyone suggest a pipeline for analysis of exome seq data?

Are you looking for snps/mutations/indels? What kind of data do you want at the end of the analysis?

[Shruti Madhiwalla]

can anyone suggest a pipeline for analysis of exome seq data?