# hicQuickQC¶

## Background¶

This tool considers the first 1,000,000 reads (or user defined number) of the mapped bam files to get a quality estimate of the Hi-C data.

## Description¶

The tool hicQuickQC considers the first n lines of two bam/sam files to get a first estimate of the quality of the data. It is highly recommended to set the restriction enzyme and dangling end parameter to get a good quality report.

usage: hicQuickQC --samFiles two sam files two sam files --QCfolder FOLDER
[--restrictionSequence RESTRICTIONSEQUENCE]
[--danglingSequence DANGLINGSEQUENCE] [--lines LINES]
[--help] [--version]


### Required arguments¶

--samFiles, -s

The two PE alignment sam files to process.

--QCfolder

Path of folder to save the quality control data of the matrix. The log files produced this way can be loaded into hicQC in order to compare the quality of multiple Hi-C libraries.

### Optional arguments¶

--restrictionSequence, -seq

Sequence of the restriction site. It is highly recommended to set this parameter to get a good quality report.

--danglingSequence

Sequence left by the restriction enzyme after cutting. Each restriction enzyme recognizes a different DNA sequence and, after cutting, they leave behind a specific “sticky” end or dangling end sequence. For example, for HindIII the restriction site is AAGCTT and the dangling end is AGCT. For DpnII, the restriction site and dangling end sequence are the same: GATC. This information is easily found on the description of the restriction enzyme. The dangling sequence is used to classify and report reads whose 5’ end starts with such sequence as dangling-end reads. A significant portion of dangling-end reads in a sample are indicative of a problem with the re-ligation step of the protocol. It is highly recommended to set this parameter to get a good quality report.

--lines

Number of lines to consider for the QC test run.

Default: 1000000

--version

show program’s version number and exit