I have pair-ended illumina samples with the read length of 100-150bp. I tried to map them to the reference genome/transcritpome, but almost nothing mapped using BWA or Bowtie.
When I blast them to nt reference using megablast, the most reads map to the right species. What does this mean? How can I interpret this? and what do I do to improve short-read alignment using BWA or bowtie?
Your question is very vague and people will probably be unable to help without further information.
What species? What type of experiment? How exactly did you run BWA and Bowtie? Can you give us some examples of reads that mapped with megablast and failed with BWA or Bowtie? What have you tried so far?