Hi,
Sorry for asking so simple questions but I am new in bioinformatics. I have some mouse RNA-seq data and I would like to align them by TopHat. I know a bit about gtf file (representing position of genes) and indexing or annotating file (e.g. hg19 or mm10) (representing function of genes). I was wondering if I am right! and if there would more information about them!
I was also wondering about library type of reads (stranded or unstranded)! and if they both work for single-end or paired-end sequences.
Thanks
Sorry for asking so simple questions but I am new in bioinformatics. I have some mouse RNA-seq data and I would like to align them by TopHat. I know a bit about gtf file (representing position of genes) and indexing or annotating file (e.g. hg19 or mm10) (representing function of genes). I was wondering if I am right! and if there would more information about them!
I was also wondering about library type of reads (stranded or unstranded)! and if they both work for single-end or paired-end sequences.
Thanks
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