Thank you very much Ashutosh Pandey. I think using galaxy platform I can do this? Right?
I am new to bioinformatics and recently I started a research project to compare promoters of a particular gene (not decided yet). I have several raw reads of WGS deposited in ENA site. How should I use these raw reads to extract a particular region? For example, sequence of the rice LEAFY gene.
1 answer
Download the data and align it against the rice reference genome. Then use the coordinates of the gene you are looking for and extract those sequences from the BAM file using samtools.
Yes, upload FASTQ, align to ref genome. Then use SAM manipulation tools and a BED file to extract the region.
Thank you RamRS. Should this BED file only contain the sequence of interest? If so, how to create it from FASTQ or FATSA file. Because I have the FASTA file of the gene of interest downloaded from the reference genome.
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