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Thread | Thread Starter | Forum | Replies | Last Post |
How to filter out chromosomes/specific regions from a BAM file? | fcr | Bioinformatics | 6 | 10-29-2018 06:24 AM |
How to filter a SAM/BAM file by bp | alisrpp | Bioinformatics | 5 | 01-17-2014 01:11 PM |
Filter paired & mapped reads from SAM/BAM file | pirates.genome | Bioinformatics | 2 | 06-19-2012 02:21 AM |
how to filter a bam file | paolo.kunder | Bioinformatics | 2 | 01-20-2012 02:07 AM |
Filter paired end BAM file based on iSize | Leif Bergsagel | Bioinformatics | 2 | 12-16-2010 12:50 PM |
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#1 |
Junior Member
Location: Brasil Join Date: Jan 2016
Posts: 1
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Hello All,
I have multiple alignments generated to DEG analysis. I know that grep for unaligned reads is not trust and the best way is the -f4 flag. But here what I want is the contigs with no alignment with those reds from specific libraries. I already have the counts matrices and I can grep those sequences from the matrix, but I want to do a sanity check . Thank's in advanced. |
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#2 |
Senior Member
Location: uk Join Date: Mar 2009
Posts: 667
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Samtools idxstats should give you a list of how many reads aligned to each of the contigs in your reference genome, i.e. the sequences that are listed in the sam/bam headers.
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