Yes the best way would be to ask the person who handled the sequencing part. Otherwise, the only way would be to map a few reads. Take the first 10,000-20,000 reads and then map then and estimate the mean insert size. Your insert size need not to be accurate and a rough estimation should be enough for the aligner.
How To Set Tophat Insert Size Without A 'Test' Run?
correctly setting 2 parameters in Tophat: --mate-inner-dist --mate-std-dev should be very important, but i have no idea how to set them without firstly running bowtie (or bowtie2) -> samtools -> picard tools, which seems a little bit redundant for Tophat.
Does any one have suggestions? Thanks in advance!!
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During sample preparation you/your lab has probably used bioanalyzer to quality control the sample. In those results you can estimate the fragment size and its standard deviation from the histogram
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