Hello!
I convert SOLiD csfasta- and qual-files to fastq-files and map those against
Hg19 (Bowtie).
I would like to use the resulting sam-files in the IGV browser (Broad
Institute).
Therefore, the sam-file need to be sorted an indexed. This could be done
using the igvtools.
However, it
Hi!
Following situation:
10 barcoded samples. Each sample consists of a mix of the sequences 3
independent genes (á 2 alleles).
I would like to map the SOLiD4 reads only to the sequences of those 3
genes, patient by patient.
First, the 10 barcoded samples have to be separated from each
2 matches
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