Hi, i have used SPades to generate contigs file for bacteria genome assembly by using 2x150 illumina paired-end reads. But when i proceed to SSPACE for contig extension, SSPACE requires library.txt as parameter. Moreover, i didnt find any files generated from SPades has this "library.txt". So my question is how can i obtain this library.txt which i believe it must be come from my own paired-end reads.
I have 150bp reads in order to eventually find the genome of bacteria. How do I know which Aligner to use (bwa or bowtie)? In addition, how do I find out what is the insert size and the error for the 4th and 5th columns in the library.txt file?
Thank you in advance.
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