Hi,
We see a peculiar bias in the mapping of reads in forward and reverse directions to sites in human genomic DNA. Occurs with both RNAseq and DNAseq, and with both novoalign and maq mapping. 45bp SE GAII data.
We thought there should be a 50%/50% split of reads mapping to the genome in forward and reverse directions. The ratios of ./, or A/a etc (maq pileup output format) have huge variance, much more than expected by chance.
Has anyone else seen this? Is it something to do with solexa chemistry - eg adapter ligation, PCR steps?
It is relevant for SNP calling algorithms.
thanks
david
We see a peculiar bias in the mapping of reads in forward and reverse directions to sites in human genomic DNA. Occurs with both RNAseq and DNAseq, and with both novoalign and maq mapping. 45bp SE GAII data.
We thought there should be a 50%/50% split of reads mapping to the genome in forward and reverse directions. The ratios of ./, or A/a etc (maq pileup output format) have huge variance, much more than expected by chance.
Has anyone else seen this? Is it something to do with solexa chemistry - eg adapter ligation, PCR steps?
It is relevant for SNP calling algorithms.
thanks
david
Comment