NGSCheckMate

NGSCheckMate is a software package for identifying next generation sequencing (NGS) data files from the same individual. It analyzes various types of NGS data files including (but not limited to) whole genome sequencing (WGS), whole exome sequencing (WES), RNA-seq, ChIP-seq, and targeted sequencing of various depths. Data types can be mixed (e.g. WES and RNA-seq, or RNA-seq and ChIP-seq). It takes BAM (reads aligned to the genome), VCF (variants) or FASTQ (unaligned reads) files as input. NGSCheckMate uses depth-dependent correlation models of allele fractions of known single-nucleotide polymorphisms (SNPs) to identify samples from the same individual. Our alignment-free module is fast (e.g., less than one minute for RNA-seq using a single core) and we recommend it for a quick initial quality check, before pooling / aligning sequenced reads. The BAM and VCF modules can be used after the alignment and variant calling steps, respectively, to ensure correct sample annotation before further downstream analysis. Currently, it works only for human data.

NGSCheckMate paper is now published in Nucleic Acids Research.

pdf documentation is included in the package. Documentation.pdf

Requirements
Installation
Usage
Examples
Input file list format
Output
Supporting scripts
Authors
Acknoledgements

Requirements

1) Software environment

- Unix/Linux System
- Python 2.6 or above
- R 3.1 or above (required to generate a PDF of sample clustering dendrogram and 
     a xgmml graphical output for sample clustering; see Output and Supporting scripts)

For the BAM module,

- samtools (tested on version 0.1.19 and 1.3.1) 
- bcftools 0.1.19 (a utility program included in samtools) 
  
  To install both programs:
  you download Samtools 0.1.19 (e.g.) https://sourceforge.net/projects/samtools/files/samtools/0.1.19/ 
  
  tar xvf samtools-0.1.19.tar.bz2
  cd samtools-0.1.19
  make

2) Additional files

For the BAM module,

- Human reference genome FASTA file (hg19 or GRCh37)
- A bed file (.bed) that lists the locations of selected SNPs (included in the package)

For the VCF module, (VCF generated by samtools or GATK)

- A bed file (.bed) that lists the locations of selected SNPs (included in the package)

For the FASTQ module,

- A binary pattern file (.pt) that lists the flanking sequences of selected SNPs (included in the package)

Installation

1) Downloading NGSCheckMate

cd <installation_dir>
git clone https://github.com/parklab/NGSCheckMate.git

## set NCM_HOME according to you shell environment 
## for example, when using bash, add the following in your .bashrc 
export NCM_HOME=<installation_dir>/NGSCheckMate

2) Configuration (required only for the BAM module)

If your input is BAM/VCF files, add the following lines in your ncm.conf file in the package directory. If your input is FASTQ files, you can skip this step.

REF=<path for the reference FASTA file >  
SAMTOOLS=<path for samtools> 
BCFTOOLS=<path for bcftools>

Buid for fastq module / patterngenerator

If you want to build your own fastq module or patterngenerator from source do the following.

cd $NCM_HOME
source install_ncmfastq.sh

Usage

1) BAM/VCF mode

Usage: python ncm.py <-B | -V> <–d INPUT_DIR | -l INPUT_LIST_FILE> <-bed BED_FILE> <–O OUTPUT_DIR> [options]

Required arguments

-B | -V		A flag that indicates an input file type (B: BAM, V: VCF)
		Input bam files need to be sorted by coordinates and indexed.

-d DIR		A directory that contains input files
  or
-l FILE		A text file that lists input files and sample names (one per line; see Input file format)

-bed FILE  	A bed format file that lists the locations of selected SNPs (included in the package) 
 		SNP/SNP_GRCh37_hg19_wChr.bed if your reference genome fasta file contains 'chr' in a chromosome name (e.g. 'chr10'). 
 		SNP/SNP_GRCh37_hg19_woChr.bed otherwise. 
       		Either file works for the VCF mode.

-O DIR		An output directory

Optional arguments

-N PREFIX   	A prefix of output files (default: output)

-f 		Use strict VAF correlation cutoffs. Recommended when your data may include related    
              	individuals (parents-child, siblings)
              	
-nz             Use the mean of non-zero depths across the SNPs as a reference depth
 		(default: Use the mean depth across all the SNPs)

2) Speed up to analyze multiple large BAM files

You may need to analyze a large number of large BAM files. For example, you may want to identify the proper pairing of 100 cancer WGS data with their matched blood WGS data sequenced at high depth. In this case, it would take a long time to run NGSCheckMate on the set of BAM files, and we recommend the following procedures.

STEP1: Generate a VCF file for each BAM file as follows. This step can be parallelized depending on your computing system. For example, the LSF-based system can perform this step in parallel using ‘bsub’ command.

# an example for generating sample.vcf from sample.bam mapped to hg19 (after 0.1.19 version)
samtools mpileup -I -uf hg19.fasta -l SNP_GRCh37_hg19_woChr.bed sample.bam | bcftools call -c - > ./sample.vcf
  
# an example for generating sample.vcf from sample.bam mapped to hg19 (0.1.19 version)
samtools mpileup -I -uf hg19.fasta -l SNP_GRCh37_hg19_woChr.bed sample.bam | bcftools view -cg - > ./sample.vcf

STEP2: Run NGSCheckMate on the set of VCF files as input.

python ncm.py -V …

3) FASTQ mode

Usage: python ncm_fastq.py <-l INPUT_LIST_FILE> <-pt PT_FILE> <–O OUTPUT_DIR> [options]

Required arguments

-l FILE		A text file that lists input fastq (or fastq.gz) files and sample names (one per line; see Input file format)

-pt FILE	A binary pattern file (.pt) that lists flanking sequences of selected SNPs (included in the package; SNP/SNP.pt)

-O DIR		An output directory

Optional arguments

-N PREFIX  	A prefix for output files (default: “output”)

-f 		Use strict VAF correlation cutoffs. Recommended when your data may include   
 		related individuals (parents-child, siblings)
 		
-nz            Use the mean of non-zero depths across the SNPs as a reference depth
 		(default: Use the mean depth across all the SNPs)

-s FLOAT	The read subsampling rate (default: 1.0)
  or
-d INT		The target depth for read subsampling. NGSCheckMate calculates a subsampling rate based on this target depth. 

-R INT		The length of the genomic region with read mapping (default: 3x10^9) used to compute subsampling rate. If your data is 		NOT human WGS and you use the -d option, it is highly recommended that you specify this value. For instance, if your data is 		human RNA-seq, the genomic length with read mapping is ~3% of the human genome (1x10^8).

-L INT		The length of the flanking sequences of the SNPs (default: 21bp). It is not recommended that you change this value 			unless you create your own pattern file (.pt) with a different length. See Supporting Scripts for how to generate 			your own pattern file.

-p INT		The number of threads (default: 1)

4) FASTQ mode (alternative way)

A C program, ngscheckmate_fastq, can be directly called to generate a VAF file from one FASTQ file (single-end sequencing) or two FASTQ files(paired-end sequencing). Then, another script, vaf_ncm.py is used to read a set of VAF files to complete the downstream analysis. When you need to analyze many FASTQ files, the first VAF file generation using ngscheckmate_fastq can be parallelized.

ngscheckmate_fastq

Usage: ngscheckmate_fastq <-1 FASTQ_FILE1> [-2 FASTQ_FILE2] <PT_FILE (.pt)> [options] > output.vaf

Required arguments

-1, --fastq1 FILE 	FASTQ file for single-end or the first FASTQ file for paired-end. File can be gzipped (auto-detect).

PT_FILE			A binary pattern file (.pt) that lists flanking sequences of selected SNPs 								(included in the package; SNP/SNP.pt)
		
Optional arguments
-2, --fastq2 FILE 	The second FASTQ file for paired-end. File can be gzipped (auto-detect).

-s, --ss FLOAT		The read subsampling rate (default: 1.0)
or
-d, --depth INT 	The target depth for read subsampling. NGSCheckMate calculates a 
			subsampling rate based on this target depth. 

-R, --reference_length INT 	The length of the genomic region with read mapping (default: 3x10^9) to compute a subsampling rate. If 				your data is NOT human WGS and you use the -d option, it is highly recommended that you specify this value. 					For nstance, if your data is human RNA-seq, the genomic length with read mapping is ~3% of the 						human genome (1x10^8).

-L, --pattern_length INT 	The length of flanking sequences of SNPs (default: 21bp). It is recommended not to change this value 					unless you create your own pattern file (.pt) with a different length. see Supporting Scripts for 					how to generate your own pattern file.

-p, --maxthread INT  	The number of threads to use (default : 1 )

vaf_ncm.py

Usage: python vaf_ncm.py -f -I <INPUT_DIR> -O <OUTPUT_DIR > <-N PREFIX>

Required arguments

-I DIR		Input directory that contains the output VAF files of ngscheckmate_fastq

-O DIR		Output directory

-N PREFIX	Ouput file prefix

-nz            	Use the mean of non-zero depths across the SNPs as a reference depth
 		(default: Use the mean depth across all the SNPs)

Input file list format

1) BAM/VCF mode

The input file that lists input BAM or VCF files (-l) needs to list one file per line.

Example:

/data/LSJ.bam
/data/LSH.bam
/data/LSI.bam

2) FASTQ mode

The input file that lists input FASTQ files (-l) should follow the format below.

Paired-end data

FASTQ_FILE1 (tab) FASTQ_FILE2 (tab) SAMPLE_NAME (\n)
Example:
/data/LSJ_R1.fastq	    /data/LSJ_R2.fastq      LSJ
/data/LSH_R1.fastq	    /data/LSH_R2.fastq	   LSH

Single-end data

FASTQ_FILE1 (tab) SAMPLE_NAME (\n)
Example:
/data/LSJ.fastq	    LSJ
/data/LSH.fastq	    LSH

Examples

1) Test sample pairing using BAM input

BAM files in /data/wgs_download/LUAD/:

python ncm.py -B -f -d /data/wgs_download/LUAD/ -O LUAD_WGS/ -N LUAD -bed SNP/SNP_GRCh37_hg19_woChr.bed

BAM files listed in bam_list_file:

python ncm.py -B -f -l bam_list_file -O output_dir -N outputfile_prefix -bed SNP/SNP_GRCh37_hg19_woChr.bed

2) Test sample pairing using VCF input

VCF files in /data/wgs_download/LUAD/:

python ncm.py -V -f -d /data/wgs_download/LUAD/ -O LUAD_WGS/ -N LUAD -bed SNP/SNP_GRCh37_hg19_woChr.bed

VCF files listed in vcf_list_file:

python ncm.py -V -f -l vcf_list_file -O output_dir -N outputfile_prefix -bed SNP/SNP_GRCh37_hg19_woChr.bed

3) Test sample pairing using FASTQ input

python ncm_fastq.py -l fastq_list.txt -O output -N ChIP_batch -p 4 -pt SNP/SNP.pt

Output

1) PREFIX_all.txt

This output file lists both matched and unmatched sample pairs with VAF correlation coefficients and representative sequencing depths.

Format

Sample1 (tab) matched/unmatched (tab) Sample2 (tab) Correlation (tab) Depth
6216-01A 	matched        	     6216-10A	      0.7957	       4.9
6216-01A	unmatched	     6324-10A	      0.2153	       15

2) PREFIX_matched.txt

This output file lists sample pairs that were predicted to be matched based on our depth-dependent VAF correlation model.

Format

Sample1 (tab) matched_or_unmatched (tab) Sample2 (tab) Correlation (tab) Depth
6216-01A	unmatched        	6216-10A  	 0.7957           4.9

3) PREFIX.pdf

This pdf file shows a dendrogram image of hierarchical clustering of samples based on VAF correlation coefficients.

Supporting scripts

1) Patterngenerator

The set of scripts in the patterngenerator folder in the package generate the .pt file used by the FSTQ module, in cases when the user wants to generate a custom .pt file. It requires a bed file containing a set of SNP positions, a genome reference file (both FASTA and bowtie 1 index) and the bowtie alignment program (http://bowtie-bio.sourceforge.net/index.shtml). Usage: makesnvpattern.pl bedfile genomefasta genome(bowtie)index outdir outprefix

2) Graph generator (Rscript)

This script with a set of xgmml templates is used for generating a graph representing matching files as connected nodes. The output format is in .xgmml, which can be read by Cytoscape.

source("graph/ngscheckmate2xgmml.R")
create.xgmml.from.ngscheckmateout(label.file,ngscheckmateoutput.file,output.xgmml)

Label file: a tab-delimited text file containing a BAM file name (1st column), an individual identifier (2nd column) and optionally, a file identifier (3rd column) for each line. An individual identifier must be unique to a subject (e.g. both tumor and normal samples from the same individual must have the same individual identifier). A file identifier must be unique to a file name.
ngscheckmateoutput.file: the output text file of NGSCheckMate. It is a tab-delimited text file containing two BAM file names (1st and 2nd columns), VAF correlation (3rd column) and average depth (4th column). It may contain either all pairs or matched pairs, depending on the option used to run NGSCheckMate. Both options may be used to run this program.
Sample label file (sample.label.txt) and ngscheckmateouput.file (sample.input.txt) can be found in the subdirectory graph/.

Authors

Software programs : Sejoon Lee, Soo Lee & Alice E. Lee

Acknowledgments

The logos ( & ) have been created by Fritz Lekschas. They are composed of the following great icons:

DNA created by Irene Hoffman (CC BY 3.0 US)
King created by Yuri Mazursky (CC BY 3.0 US)
Queen created by Yuri Mazursky (CC BY 3.0 US)

parklab/NGSCheckMate

parklab

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Repository Details

NGSCheckMate

Table of contents

Requirements

1) Software environment

2) Additional files

Installation

1) Downloading NGSCheckMate

2) Configuration (required only for the BAM module)

Buid for fastq module / patterngenerator

Usage

1) BAM/VCF mode

2) Speed up to analyze multiple large BAM files

3) FASTQ mode

4) FASTQ mode (alternative way)

Input file list format

1) BAM/VCF mode

2) FASTQ mode

Examples

1) Test sample pairing using BAM input

2) Test sample pairing using VCF input

3) Test sample pairing using FASTQ input

Output

1) PREFIX_all.txt

2) PREFIX_matched.txt

3) PREFIX.pdf

Supporting scripts

1) Patterngenerator

2) Graph generator (Rscript)

Authors

Acknowledgments

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