Search Results
Search type | Search syntax |
---|---|
Tags | [tag] |
Exact | "words here" |
Author |
user:1234 user:me (yours) |
Score |
score:3 (3+) score:0 (none) |
Answers |
answers:3 (3+) answers:0 (none) isaccepted:yes hasaccepted:no inquestion:1234 |
Views | views:250 |
Code | code:"if (foo != bar)" |
Sections |
title:apples body:"apples oranges" |
URL | url:"*.example.com" |
Saves | in:saves |
Status |
closed:yes duplicate:no migrated:no wiki:no |
Types |
is:question is:answer |
Exclude |
-[tag] -apples |
For more details on advanced search visit our help page |
Questions specific to interacting with and post-processing sequence alignments using the SAMtools package. For questions specifically about formats SAM, BAM or CRAM use tags sam or bam,
1
vote
2
answers
99
views
Using preprocessing/alignment functions on the server
I have a series of raw RNA sequencing files: .bam and wish to utilize samtools (or others) to begin the data preprocessing steps defined in many workflows. … : -bash-samtools: command not found
When I try to install the package, say samtools, by running sudo apt install samtools, I get an error stating I do not have permission to do such. …
3
votes
1
answer
2k
views
Running htseq-count over BAM files
I have read the htseq-count documentation as well as samtools and figured that the following command should work:
samtools sort -on file.bam | samtools view -h - | htseq-count --type=exon --idattr=gene_id … Just note that the newer versions of htseq-count don't require sorted .bam files and, so following the editing of the .gtf file, all I needed to do was convert it to .sam using samtools view -h and then …
3
votes
2
answers
316
views
Frequency of specific viral sequence in .BAM or .fastq
So, my question is: if I were to use samtools - or any other program - to convert the .bam files to .fastq, is there any possibility that I could lose such information - e.g. viral seqs - that would have …