Hi!
I tried comparing the result of wANNOVAR and ANNOVAR using the same file. Only 464 rows matched! Can someone help me to improve my result & bring the same result as wANNOVAR?
TIA!
Hi, I'm trying to annotate my VCF file with wAnnovar and have received the following message: User input contains 33631 lines WARNING: 33574 invalid alternative …
I am using Genesum package for estimating gene abundnace from transcript abundance. As input, I give sailfish generated expression file "Quant.sf" and gene annotation "GTF" …
Please show all of your processing steps.