Thank you so much!
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Hi all,
Could you please suggest the most highly cited, user-friendly, reproducible, and free pipelines from git-hub repositories for COVID-19 data analysis. The input files should be paired-end fastq files (Illumina) or fasta file from assembled reads, and the output should be the consensus sequence, VCF file with mutations, and the table with interpretation. It will be great if there is some minimal database with the interpretation of a particular list of SNPs. I will be thankful for any suggestions!
Thank you so much!
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Does it need a function to submit to Nature right away or is that optional?
)))) it is not necessary )