SEQanswers

Go Back   SEQanswers > Bioinformatics > Bioinformatics



Similar Threads
Thread Thread Starter Forum Replies Last Post
hg19 genome reference for short read mapping yh253 Bioinformatics 4 12-29-2013 09:11 PM
Alignment to selected region of the reference genome houkto General 1 02-20-2012 05:51 AM
Assisted de novo genome assembly? Create new consensus mapping reads to reference? zmartine Bioinformatics 8 02-10-2012 12:31 AM
alignment and reference genome assembling slny Bioinformatics 3 03-16-2011 06:49 AM
Reference genome for MAQ - split reference genome by chromosome or not? inesdesantiago Bioinformatics 4 02-18-2009 08:44 AM

Reply
 
Thread Tools
Old 08-18-2011, 12:17 PM   #1
KAP
Member
 
Location: Adelaide, Australia

Join Date: Mar 2010
Posts: 12
Default Please help: imperfect reference genome/get consensus on genome/read alignment?

I an doing RNA-seq on two closely related plant species (~98% similar in transcript region), one of which is sequenced.

My problem comes when I align the reads from the unsequenced species to the sequenced genome. Most of the reads align (at 2 bp mismatch level), however some are being rejected due to 3 or 4 bp mismatches. I would like to improve on the alignability of reads/reference genome to ensure the observed differences in expression between species are true (not due to differences in read alignability).

My idea is as follows:
  1. Align the reads to the reference (allow ~2 bp mismatch)
  2. Use the alignment to generate a consensus sequence, ie where there are SNPs between the reference and the reads, change the base on the chromosome to reflect that of the reads. Use stringent parameters so only true SNPs are 'corrected'.
  3. Realign the reads to the modified genome (allow ~2 bp mismatch). Now reads with 2 bp mismatches should align 'perfectly' and reads with up to 4 bp mismatches will align.

Can anyone recommend programs or a strategy to do this, or even comment on the validity of the approach?

Any feedback/contribution would be much appreciated! Thank you!!

Note: the reads are very short: 40 bp.
KAP is offline   Reply With Quote
Old 08-19-2011, 07:14 AM   #2
macrowave
Member
 
Location: New York

Join Date: May 2010
Posts: 13
Default

I had the similar idea when facing a somewhat similar situation. In theory, this would work, but in practice, I found the transcript levels quantified from the 'reconstructed' genome are biased towards lower end. I suspected that these didn't reflect the true expression levels in the 'reconstructed' species, skewed towards underestimation. I haven't thought about the exact causes, but I think it's related to the 'reconstruction' process and the heterogeneity of genomic divergence along chromosomes between two species. So in the end, I just mapped to the same reference, but allowing extra mismatches for the divergent species. Another way to look into this is just going ahead and to do a de novo assembly for the divergent species, but that opens a can of worms, too. And it's a complete different ball game.

Last edited by macrowave; 08-22-2011 at 06:51 AM.
macrowave is offline   Reply With Quote
Reply

Tags
alignment, differential expression, rna-seq, software

Thread Tools

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off




All times are GMT -8. The time now is 08:37 AM.


Powered by vBulletin® Version 3.8.9
Copyright ©2000 - 2020, vBulletin Solutions, Inc.
Single Sign On provided by vBSSO