Skip to content

Latest commit

 

History

History
254 lines (151 loc) · 14.1 KB

README.md

File metadata and controls

254 lines (151 loc) · 14.1 KB
Raw

MindTheGap

Linux Mac OSX
Build Status Build Status

install with bioconda

License

What is MindTheGap ?

MindTheGap performs detection and assembly of DNA insertion variants in NGS read datasets with respect to a reference genome. It is designed to call insertions of any size, whether they are novel or duplicated, homozygous or heterozygous in the donor genome. It takes as input a set of reads and a reference genome. It outputs two sets of FASTA sequences: one is the set of breakpoints of detected insertion sites, the other is the set of assembled insertions for each breakpoint.

New ! MindTheGap can also be used as a genome assembly finishing tool: it can fill the gaps between a set of input contigs without any a priori on their relative order and orientation. It outputs the results in a gfa file. It is notably integrated as an essential step in the targeted assembly tool MinYS (MineYourSymbiont in metagenomics datasets, see https://github.com/cguyomar/MinYS).

MindTheGap is a Genscale tool, built upon the GATB C++ library, and developed by:

  • Claire Lemaitre
  • Cervin Guyomar
  • Wesley Delage
  • Guillaume Rizk
  • Former developers: Rayan Chikhi, Pierre Marijon.

Installation instructions

Requirements

CMake 3.1+; see http://www.cmake.org/cmake/resources/software.html

C++/11 capable compiler (e.g. gcc 4.7+, clang 3.5+, Apple/clang 6.0+)

Getting the latest source code with git

# get a local copy of MindTheGap source code
git clone --recursive https://github.com/GATB/MindTheGap.git

# compile the code
cd MindTheGap
sh INSTALL
# the binary file is located in directory build/bin/
./build/bin/MindTheGap -help

Note: when updating your local repository with git pull, if you see that thirdparty/gatb-core has changed, you have to run also : git submodule update.

Installing a stable release

Retrieve a binary archive file from one of the official MindTheGap releases (see "Releases" tab on the Github web page); file name is MindTheGap-vX.Y.Z-bin-Linux.tar.gz (for Linux) or MindTheGap-vX.Y.Z-bin-Darwin.tar.gz (for MacOs).

tar -zxf MindTheGap-vX.Y.Z-bin-Darwin.tar.gz
cd MindTheGap-vX.Y.Z-bin-Darwin
chmod u+x bin/MindTheGap
./bin/MindTheGap -help

In case the software does not run appropriately on your system, you should consider to install it from its source code. Retrieve the source archive file MindTheGap-vX.Y.Z-Source.tar.gz.

tar -zxf MindTheGap-vX.Y.Z-Source.tar.gz
cd MindTheGap-vX.Y.Z-Source
sh INSTALL
# the binary file is located in directory build/bin/
./build/bin/MindTheGap -help

Using conda or docker

MindTheGap is also distributed as a Bioconda package:

conda install -c bioconda mindthegap

Or pull the docker image of MindTheGap (warning: need to be updated with latest releases):

docker pull clemaitr/mindthegap

Small run example

MindTheGap find -in data/reads_r1.fastq,data/reads_r2.fastq -ref data/reference.fasta -out example
MindTheGap fill -graph example.h5 -bkpt example.breakpoints -out example

USER MANUAL

Description

MindTheGap is a software that performs integrated detection and assembly of genomic insertion variants in NGS read datasets with respect to a reference genome. It is designed to call insertions of any size, whether they are novel or duplicated, homozygous or heterozygous in the donor genome.

Alternatively and since release 2.1.0, MindTheGap can also be used as a genome assembly finishing tool. It is integrated as an essential step in the targeted assembly tool MinYS (MineYourSymbiont in metagenomics datasets). It takes also part of a gap-filling pipeline dedicated to linked-read data (10X Genomics): MTG-link.

Insertion variant detection

It takes as input a set of reads and a reference genome. Its main output is a VCF file, giving for each insertion variant, its insertion site location on the reference genome, a single insertion sequence or a set of candidate insertion sequences (when there are assembly ambiguities), and its genotype in the sample.

For a detailed user manual specific to insertion variants see doc/MindTheGap_insertion_caller.md.

Genome assembly gap-filling (New feature !)

When given a set of reads and a set of contigs as input, MindTheGap tries to fill the gaps between all pairs of contigs by de novo local assembly without any a priori on their relative order and orientation. It outputs the results in gfa file.

For a detailed user manual specific to contig gap-filling see doc/MindTheGap_assembly.md.

Performances

MindTheGap performs de novo assembly using the GATB C++ library and inspired from algorithms from Minia. Hence, the computational resources required to run MindTheGap are significantly lower than that of other assemblers (for instance it uses less than 6GB of main memory for analyzing a full human NGS dataset).

For more details on the method and some recent results, see the web page.

Usage and examples

MindTheGap is composed of two main modules : breakpoint detection (find module) and the local assembly of insertions or gaps (fill module). Both steps are implemented in a single executable, MindTheGap, and can be run independently by specifying the module name as follows :

MindTheGap <module> [module options]

  1. Basic command lines

     #Find module:
 MindTheGap find (-in <reads.fq> | -graph <graph.h5>) -ref <reference.fa> [options]
 #To get help:
 MindTheGap find -help
 
 #Fill module:
 MindTheGap fill (-in <reads.fq> | -graph <graph.h5>) (-bkpt <breakpoints.fa> | -contig <contigs.fa>) [options]
 #To get help:
 MindTheGap fill -help

  2. Examples

    These examples can be run with the small datasets in directory data/

    Example for insertion variant calling:

     #find
 build/bin/MindTheGap find -in data/reads_r1.fastq,data/reads_r2.fastq -ref data/reference.fasta -out example
 # 3 files are generated: 
 #   example.h5 (de bruijn graph), 
 #   example.othervariants.vcf (SNPs and deletion variants), 
 #   example.breakpoints (breakpoints of insertion variants).
 
 #fill
 build/bin/MindTheGap fill -graph example.h5 -bkpt example.breakpoints -out example
 # 3 files are generated:
 #   example.insertions.fasta (insertion sequences)
 #   example.insertions.vcf (insertion variants)
 #   example.info.txt (log file)

    Example for gap-filling between contigs:

    build/bin/MindTheGap fill -in data/contig-reads.fasta.gz -contig data/contigs.fasta -abundance-min 3 -out contig_example
# 4 files are generated
#   contig_example.h5 (de bruijn graph)
#   contig_example.insertions.fasta (gap-filling sequences)
#   contig_example.gfa (genome graph)
#   contig_example.info.txt (log file)

    The usage of the fill module is a little bit different depending on the type of gap-filling : assembling insertion variants (using the -bkptoption with a breakpoint file) or gap-filling between contigs (using the -contig option with a contig fasta file).

Details

  1. Input sequencing read data

    For both modules, read dataset(s) are first indexed in a De Bruijn graph. The input format of read dataset(s) is either the read files themselves (option -in), or the already computed de bruijn graph in hdf5 format (.h5) (option -graph).
    NOTE: options -in and -graph are mutually exclusive, and one of these is mandatory.

    If the input is composed of several read files, they can be provided as a list of file paths separated by a comma or as a "file of file" (fof), that is a text file containing on each line the path to each read file. All read files will be treated as if concatenated in a single sample. The read file format can be fasta, fastq or gzipped.

  2. de Bruijn graph creation options

    In addition to input read set(s), the de Bruijn graph creation uses two main parameters, -kmer-size and -abundance-min:

    • -kmer-size: the k-mer size [default '31']. By default, the largest kmer-size allowed is 128. To use k>128, you will need to re-compile MindTheGap as follows:

      cd build/
cmake -DKSIZE_LIST="32 64 96 256" ..
make

      To go back to default, replace 256 by 128. Note that increasing the range between two consecutive kmer-sizes in the list can have an impact on the size of the output h5 files (but none on the results).

    • -abundance-min: the minimal abundance threshold, k-mers having less than this number of occurrences are discarded from the graph [default 'auto', ie. automatically inferred from the dataset].

    • -abundance-max: the maximal abundance threshold, k-mers having more than this number of occurrences are discarded from the graph [default '2147483647' ie. no limit].

  3. Computational resources options

    Additional options are related to computational runtime and memory:

    • -nb-cores: number of cores to be used for computation [default '0', ie. all available cores will be used].
    • -max-memory: max RAM memory for the graph creation (in MBytes) [default '2000']. Increasing the memory will speed up the graph creation phase.
    • -max-disk: max usable disk space for the graph creation (in MBytes) [default '0', ie. automatically set]. Kmers are counted by writing temporary files on the disk, to speed up the counting you can increase the usable disk space.

  4. MindTheGap Output

    All the output files are prefixed either by a default name: "MindTheGap_Expe-[date:YY:MM:DD-HH:mm]" or by a user defined prefix (option -out of MindTheGap).

    The main results files are output by the Fill module, these are:

    • an insertion variant file (.insertions.vcf) in vcf format, in the case of insertion variant detection (for insertions >2 bp).

    • an assembly graph file (.gfa) in GFA format, in the case of contig gap-filling. It contains the original contigs and the obtained gap-fill sequences (nodes of the graph), together with their overlapping relationships (arcs of the graph).

    Additional output files are:

    • a graph file (.h5), output by both MindTheGap modules. This is a binary file containing the de Bruijn graph data structure. To obtain information stored in it, you can use the utility program dbginfo located in your bin directory or in ext/gatb-core/bin/.

    • Files output specifically by MindTheGap find:

      • a breakpoint file (.breakpoints) in fasta format.

      • a variant file (.othervariants.vcf) in vcf format. It contains SNPs, deletions and very small insertions (1-2 bp).

    • Files output specifically by MindTheGap fill:

      • a sequence file (.insertions.fasta) in fasta format. It contains the inserted sequences (for insertions >2 bp) or contig gap-fills that were successfully assembled.

      • a log file (.info.txt), a tabular file with some information about the filling process for each breakpoint/grap-fill.

      • with option -extend, an additional sequence file (.extensions.fasta) in fasta format. It contains sequence extensions for failed insertion or gap-filling assemblies, ie. when the target kmer was not found, the first contig immediately after the source kmer is output.

​

Other optional parameters and details on input and output file formats are given in doc/MindTheGap_insertion_caller.md and doc/MindTheGap_assembly.md, depending on the usage.

Utility programs

Either in your bin/ directory or in ext/gatb-core/bin/, you can find additional utility programs :

  • dbginfo : to get information about a graph stored in a .h5 file
  • dbgh5 : to build a graph from read set(s) and obtain a .h5 file
  • h5dump : to extract data stored in a .h5 file

Reference

If you use MindTheGap, please cite:

MindTheGap: integrated detection and assembly of short and long insertions. Guillaume Rizk, Anaïs Gouin, Rayan Chikhi and Claire Lemaitre. Bioinformatics 2014 30(24):3451-3457. http://bioinformatics.oxfordjournals.org/content/30/24/3451

Web page with some updated results.

MindTheGap was also evaluated in a recent benchmark exploring many different genomic features (size, nature, repeat context, junctional homology at breakpoints) of human insertion variants. Among other tested SV callers, MindTheGap was the only tool able to output sequence-resolved insertions for many types of insertions. Read more: Towards a better understanding of the low recall of insertion variants with short-read based variant callers. Delage W, Thevenon J, Lemaitre C. BMC Genomics 2020, 21(1):762.

Contact

To contact a developer, request help, or for any feedback on MindTheGap, please use the issue form of github: https://github.com/GATB/MindTheGap/issues

You can see all issues concerning MindTheGap here and GATB here.

If you do not have any github account, you can also send an email to claire dot lemaitre at inria dot fr