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3.9 years ago
priya.saxena
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10
While using Featurecounts tool, I am getting zero counts for RNA seq reads, It can be due to unmatched chromosome identifiers in BAM and GTF file. Can someone please help me out in making the identifiers same for both the file?
Thank You
How can this be? Usually one uses a reference genome that matches the GTF. What species is this and where are the files from?
Yes, I used the reference genome and then I did the mapping with Bowtie2 to generate a BAM file. This BAM file and the gtf file from NCBI RefSeq was used as input for Featurecounts. The species used is Desulfovibrio alaskensis G20 from NCBI RefSeq. The FTP link is from where I uploaded GTF and genome sequence to galaxy is the following
https://ftp.ncbi.nlm.nih.gov/genomes/all/GCF/000/012/665/GCF_000012665.1_ASM1266v1/
Which files did you exactly use?
Try using this for genome: GCF_000012665.1_ASM1266v1_genomic.fna.gz
And this for gtf: GCF_000012665.1_ASM1266v1_genomic.gtf.gz
Both are coming from: https://ftp.ncbi.nlm.nih.gov/genomes/all/GCF/000/012/665/GCF_000012665.1_ASM1266v1/
This should work, good luck!
Thank You so much I will try this and let you know.