Dear All,
I am new to Whole genome sequencing analysis. I have two sample fastq files. I have run fastqc and bowtie2 using reference genome (papaya). I got the sam file. Now How to computationally identify the list of genes and their locations present in my file. I need all the gene list. So I can find GO annotations
Hi, i have some problem, i mean i want to extract gene list from 200 GTF file E.coli sequences but the problem is how can i separate a gene which are not annotated or present in gff file with their gene name.
Thank you