Shalabh,
Not to toot my own horn, but I believe lastz should do a better job
than bwa for reads longer than about 100 bp. bwa will run faster, but
my understanding is that it will not find many reads with more than 3
mismatches. Moreover, if your reads are from 454, which is subject to
short indel sequencing errors, I believe reads with these errors will
generally be missed by bwa.
I good test on your data would be to take a random sample of 10,000
reads and try mapping them with both tools, and see which one gives
you more believable results.
You could also post your question to seqanswers.com-- describe your
data (dna or rna, read lengths, sequencing technology, expected
divergence between your sample and the reference, how you prefer non-
uniquely aligning reads to be handled, etc.) and ask for advice about
the pros and cons of different aligners/mappings.
Bob H
On Oct 4, 2011, at 8:21 PM, Jennifer Jackson wrote:
Hello Shalabh,
BWA is a good choice for longer reads, if they are DNA. If you have
RNA data, then you might want to consider a tool like BLAT or BLAST
(is wrapped for Galaxy in the Tool Shed).
To use BLAST in Galaxy, you will need a local or cloud instance, as
explained here:
http://getgalaxy.org
http://galaxyproject.org/wiki/Tool%20Shed
Hopefully this helps,
Jen
Galaxy team
On 10/3/11 7:50 AM, Shalabh Sharma wrote:
Hi,
I am new to mapping.
I have reads ranging from 150-300bp, i am not sure which is the best
suitable program for that in Galaxy.
I already tried bwa but i am not sure if thats the best choice for
long
reads.
Thanks
Shalabh
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