Dear all,
In attachment the result of mapping for 32-36bp length reads.
Most of the hits are to supercontigs.
Here is the possible explanation:
In alignments a lot of reads map to GL000220.1.
My colleague Mat Davis  found the following explanation online from Ian 
Dunham (Ensembl) regarding someone else's question:
  "In human the ribosomal RNA gene clusters containing the 28S, 18S and 
5.8S RNAs are located on the short arms of the acrocentric chromosomes 
(13, 14, 15, 21 and 22) in long repeating arrays of 40 odd kb for a 
single unit. You have many copies in the arrays and copy number is 
variable between individuals. These regions are difficult to assemble 
into what are now called supercontigs because of this repeating 
structure and other satellite repeats that lie on these chromosome arms, 
so although there have been some BACs sequenced representing the 
clusters, the contigs are not integrated into the chromosome 
supercontigs. Instead they lie on the set of unplaced supercontigs. 
Supercontig GL000220.1 for instance is one of these. There are others. 
In the sequence databases there are several BACS that cover these 
clusters."
So it seems the mapping to rRNAs and to supercontigs is related.
Regards,
Natalja
  On 2/23/12 11:37 AM, Tuuli Lappalainen wrote:
  Dear all,
 We'll have our Geuvadis RNAseq analysis group call again today 
 (Thursday) at 2pm.
 Things to be discussed:
 - update on sequencing progress
 - miRNA QC issues
 - Tuuli will present some slides on how genetic variants affect 
 mapability, and ways to correct for it
 - mRNA and miRNA data processing pipelines
 Call details:
 Spain
 	
 902 125 136
 Other countries
 	
 +34 91 495 18 99
 Participants' Pin-code:
 	
 764989*
 best regards,
 Tuuli
 -- 
 Tuuli Lappalainen, PhD
 Department of Genetic Medicine and Development
 University of Geneva Medical School
 CMU / Rue Michel-Servet 1
 1211 Geneva 4
 Switzerland
 Tel. +41-(0)22-3795550
 tuuli.lappalainen(a)unige.ch 
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-- 
Natalja Kurbatova, PhD
Functional Genomics Group, EBI