Hello Teja,
Exploring the "Pages" tutorials is recommended as many have SNP-specific
analysis examples. I am not sure if your data is RNA or DNA or if you
have quality scores available, but there are tutorials that cover most
common-use cases.
http://main.g2.bx.psu.edu/page/list_published
I
Hello Teja,
If you have a fasta file of sequences, you can map them to a reference
genome to obtain a SAM file (which you could then compress into BAM).
See the tool section "NGS Toolbox".
BLAST is an alignment tool and additional parsing/analysis tools would
be needed in order to identify S
2 matches
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