unrelated to bioinformatics

Don't forget to follow up on your threads. If an answer was helpful, you should upvote it; if the answer resolved your question, you should mark it as accepted. You can accept more than one answer if they all work. If an answer was not really helpful or did not work, provide detailed feedback so others know not to use that answer.

• merging tetraploid vcf files through bcftools
• Variant calling of GBS data
• Illumina NextSeq 500 Read Length
• Differential expression analysis of lncRNA
• gatk SelectVariants is giving duplicate allele error while extracting SNPs out of vcf file
• N50 value of bacterial assembly is not half of total assembly size
• Tool for structural variation detection of plant WGS data
• Tools for reference-guided de novo assembly of bacterial genome
• Building reference dbSNP file using WGS samples
• Good alignment rate for DNA-seq data

It might be better for you to post on stackoverflow (either ask ubuntu or super user). A quick check could be to run df -h or du -h | sort -h on your HOME to see where all the space is going.