Thanks swbarnes2!
I need to extract the sequences of 3 or 4 genes only not all genes
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I have performed variant calling and annotation analysis from WGS data. Now I need to get sequences of few genes containing variants.
How can I get sequences of particular variant containing genes?
It's tricky to get full sequences out of a bam, so your best bet is to make a fixed consensus sequence using your original reference fasta and your vcf.
Thanks swbarnes2!
I need to extract the sequences of 3 or 4 genes only not all genes
It's probably simpler to just make the whole altered consensus, then pick out what you want, instead of only making the consensus for 4 regions. You can also then realign to that consensus and see if your genes of interest look good in IGV.
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I know this isn't the exact answer to your question but the most common workflow to see the impact of variants on genes is to run a variant effect predictor
OP seems to have at least tried doing this (if it the same data): building snpeff database for plant
Yes I have done variant annotation.
Its rice data, I used available rice database from snpEff.
My PI wants to perform structural analysis too like comparing structure of normal gene structure with annotated gene containing variant.
Therefore I would need to extract gene sequences for only 3 or 4 genes from our WGS data.
Your guidance is highly appreciated.
Thankyou!