Purpose
SALSA (Simple AssembLy ScAffolder) is a scaffolding tool based on a computational method that exploits the genomic proximity information in Hi-C data sets for long range scaffolding of de novo genome assemblies.
Mapping reads
To start the scaffolding, first step is to map reads to the assembly. We recommend using BWA or BOWTIE2 aligner to map reads. The read mapping generates a bam file. SALSA requires BED file as the input. This can be done using the bamToBed command from the Bedtools package. Also, SALSA requires BED files to be sorted by the read name, rather than the alignment coordinates. Once you have bam file, you can run following commands to get the bam file needed as an input to SALSA.
Since Hi-C reads and alignments contain experimental artifacts, the alignments needs some postprocessing. To align and postprocess the alignments, you can use the pipeline released by Arima Genomics which can be found in the GitHub repository.
Additional information on how to generate/filter the bam here.