Error : samtools tview
Hi: I have a sorted and merged BAM file, and I would like to check the alignment, but the result is wrong. So, where is the problem? Thanks a lot.
The wrong result:
$ samtools tview KPGP-00001_picard_sort.bam /DataBase/Human/hg19/hg19.fa
1 11 21 31 41 51 61 71
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
• 2,620 views
•
link
1 answer
I found it was because the wrongly samtools installed conda, and I installed it with source code and got the right result. I have submitted this issue at https://github.com/conda/conda/issues/6191 .
• 0 views
•
link
Log in to answer this question.
samtools tviewis not the most powerful genome browser available, I would recommend IGV, IGB or Tablet (among others) to get a richer view of alignments.How is the result wrong? You mean the long stretch of Ns? Try going to some position - press
gthen write down the position, something likechr1:156000.See some further discussion here.
all the result was only 71bp and END, but obvious human genome greater, so where is the other sequence?
hu ? kamoulox ?
XRef: https://github.com/samtools/samtools/issues/728