Collecting phenotypes from ENA and make their SNPs
In this code by using the phenotypes id in the "FILE_NAME".txt file we will download its .fastq files from ENA databese
In this code by using the phenotypes id in the "FILE_NAME".txt file and its .fastq files we will make its SNP using bwa and samtools and GATK and get the common SNP of both files and store in ("Final_" + id + ".vcf")
If the code fail in make SNP of special phenotype, the id will be write in the "missIdForSNP.txt"
By calling preprocessing() function you will get the ( "Final_" + id + "_table.csv" ) file which contatin "pos, ref, alt" for each SNP
In this code we make a table for all the isolates
Will store the table of tableCreatorGit.py in the sparse format to reduce size