Hi.
I'm getting "floating point exception" error using samtools tview the following way:
$ samtools view -hb ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/data/NA12891/alignment/NA12891.chrom1.ILLUMINA.bwa.CEU.high_coverage.20100517.bam 1:157,200,000-157,300,00 > NA12891.chrom1.ILLUMINA.bwa.CEU.high_coverage.20100517_chr1-157200K-157300K.bam
$ samtools index NA12891.chrom1.ILLUMINA.bwa.CEU.high_coverage.20100517_chr1-157200K-157300K.bam
$ samtools tview NA12891.chrom1.ILLUMINA.bwa.CEU.high_coverage.20100517_chr1-157200K-157300K.bam human_g1k_v37.fasta
I've googled for this error message but I could not find anything similar to this issue.
I have tried to compile samtools source (v0.1.18) on my ubuntu system but it doesn't help.
Where is the bug reporting system for samtools? (I'd like to make sure there is no existing bug and/or workaround).
Am I using the tool is an incorrect way?
Thanks!
this is a 64 bit machine
yes of course, no problem, but prior to report a bug I would like to know to check whether it is actually a bug or if I am using the tool in an incorrect way – Pascal 0 secs ago