Run the command 1 outside the docker image mounting the personal home directory inside the docker image:
> docker run -v $HOME:/home/$USER --rm -it biofold/meta-snp:full python /home/bass/Meta-SNP/metasnp.py /home/bass/Meta-SNP/Test/fileseq.seq /home/bass/Meta-SNP/Test/filemuts.txt -o /home/$USER/test/output.txt -d /home/$USER/test/ -o /home/$USER/test/output.txt
Capriotti E, Altman RB, Bromberg Y (2013). Collective judgment predicts disease-associated single nucleotide variants. BMC Genomics. 14 Suppl 3:S2. PMID:23819846.
Capriotti E, Calabrese R, Casadio R (2006). Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information. Bioinformatics. 22(22):2729-2734. PMID:16895930.
Thomas PD, Kejariwal A (2004) Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects. Proc Natl Acad Sci USA.101(43):15398-15403. PMID:15492219.
Bromberg Y, Rost B (2007). SNAP: predict effect of non-synonymous polymorphisms on function. Nucleic Acids Res 35(11):3823-3835. PMID:17526529.
Ng PC, Henikoff S (2003). SIFT: Predicting amino acid changes that affect protein function. Nucleic Acids Res. 31(13):3812-3814.. PMID:12824425.