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Inflated alignment stats

Open caleblareau opened this issue 8 years ago • 3 comments

Can get over 100% mapping from current bowtie2 parse

caleblareau avatar May 21 '17 14:05 caleblareau

Hi, We have run Hichipper on the HiC-pro outfiles and find that the number of Mapped_unique_quality reads reported is higher than Total_PETs. How is that possible? Are we missing something here. I am attaching one of the stat files as example. example.stat.txt

Thanks

smza avatar May 04 '18 10:05 smza

The # of mapped unique quality interactions is derived from this:

cat "${WK_DIR}/${HICPRO_OUT}/hic_results/data/${SAMPLE}/"*Pairs | wc -l | awk '{print $1}'

What version of HiC-Pro are you using?

caleblareau avatar May 04 '18 15:05 caleblareau

Thanks for your prompt response. We are using HiC-Pro 2.10.0

The problem was that hi-chipper is counting the valid pairs files twice. hic_results folder contains the following 2 files where file 2 is a subset of file 1:

  1. sample1_trim_genome.bwt2pairs.validPairs

  2. sample1_allValidPairs

So ideally it should be using only file2(sample1_allValidPairs) for counting, which is the deduplicated interaction file, isn't it?

I would like a to ask a couple of more questions as follows:

  1. we would to like to know what should be the threshold for “% of fraction of total reads that are in loops" to be considered a good quality ChIP. We have seen in your

H3K27ac data the % is ~1%. Will this be considered a good or a bad quality chip efficiency or is it dependent on the antibody efficiency and other experimental factors?

  1. How do you evaluate the biological and/or technical replicate consistency? Do you have any QC metrics for doing so?

Many thanks.

Munazah

On Fri, May 4, 2018 at 4:22 PM, Caleb Lareau [email protected] wrote:

The # of mapped unique quality interactions is derived from this:

cat "${WK_DIR}/${HICPRO_OUT}/hic_results/data/${SAMPLE}/"*Pairs | wc -l | awk '{print $1}'

What version of HiC-Pro are you using?

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smza avatar May 04 '18 16:05 smza