A genomics processing engine and specialized file format built using Apache Avro, Apache Spark and Parquet. Apache 2 licensed.
Current genomic file formats are not designed for distributed processing. ADAM addresses this by explicitly defining data formats as Apache Avro objects and storing them in Parquet files. Apache Spark is used as the cluster execution system.
The Sequencing Alignment Map (SAM) and Binary Alignment Map (BAM) file specification defines a data format for storing reads from aligners. The specification is well-written but provides no tools for developers to implement the format. Developers have to hand-craft source code to encode and decode the records which is error prone and an unneccesary hassle.
In contrast, the ADAM specification for storing reads is defined in the Avro Interface Description Language (IDL) which is directly converted into source code. Avro supports a number of computer languages. ADAM uses Java; you could just as easily use this Avro IDL description as the basis for a Python project. Avro currently supports c, c++, csharp, java, javascript, php, python and ruby.
The SAM/BAM format is record-oriented with a single record for each read. However, the typical data access pattern is column oriented, e.g. search for bases at a specific position in a reference genome. The BAM specification tries to support this pattern by defining a format for a separate index file. However, this index needs to be regenerated anytime your BAM file changes which is costly. The index does help cost down on file seeks but the columnar store ADAM uses reduces seeks even more.
Once you convert your BAM file to ADAM, it can be directly accessed by Hadoop Map-Reduce, Spark, Shark, Impala, Pig, Hive, whatever. Using ADAM will unlock your genomic data and make it available to a broader range of systems.
You will need to have Maven installed in order to build ADAM.
Note: The default configuration is for Hadoop 2.2.0. If building against a different version of Hadoop, please edit the build configuration in the
<properties>section of thepom.xmlfile.
$ git clone git@github.com:bigdatagenomics/adam.git
$ cd adam
$ mvn clean package
...
[INFO] ------------------------------------------------------------------------
[INFO] BUILD SUCCESS
[INFO] ------------------------------------------------------------------------
[INFO] Total time: 9.647s
[INFO] Finished at: Thu May 23 15:50:42 PDT 2013
[INFO] Final Memory: 19M/81M
[INFO] ------------------------------------------------------------------------
Once successfully built, you'll see a single jar file named adam-X.Y-SNAPSHOT.jar in the adam-cli/target directory. This single jar
has all the dependencies you need in it. You can copy this single jar file to any machine you want to launch ADAM jobs from.
You might want to take a peek at the scripts/jenkins-test script and give it a run. It will fetch a mouse chromosome, encode it to ADAM
reads and pileups, run flagstat, etc. We use this script to test that ADAM is working correctly.
The ADAM jar file is a self-executing jar file with all dependencies included.
You might want to add the following to your .bashrc to make running adam easier:
adam_jar="/workspace/adam/adam-cli/target/adam-0.6.0-SNAPSHOT.jar"
alias adam="java -Xmx4g -jar $adam_jar"
Of course, you will want to change the adam_jar variable to point to the directory
you placed ADAM on your local filesystem. You can also modify -Xmx4g to either give
ADAM more or less memory depending on your system.
Once this alias is in place, you can run adam by simply typing adam at the commandline, e.g.
$ adam
e 888~-_ e e e
d8b 888 \ d8b d8b d8b
/Y88b 888 | /Y88b d888bdY88b
/ Y88b 888 | / Y88b / Y88Y Y888b
/____Y88b 888 / /____Y88b / YY Y888b
/ Y88b 888_-~ / Y88b / Y888b
Choose one of the following commands:
transform : Convert SAM/BAM to ADAM format and optionally perform read pre-processing transformations
flagstat : Print statistics on reads in an ADAM file (similar to samtools flagstat)
reads2ref : Convert an ADAM read-oriented file to an ADAM reference-oriented file
mpileup : Output the samtool mpileup text from ADAM reference-oriented data
print : Print an ADAM formatted file
aggregate_pileups : Aggregate pileups in an ADAM reference-oriented file
listdict : Print the contents of an ADAM sequence dictionary
compare : Compare two ADAM files based on read name
compute_variants : Compute variant data from genotypes
bam2adam : Single-node BAM to ADAM converter (Note: the 'transform' command can take SAM or BAM as input)
adam2vcf : Convert an ADAM variant to the VCF ADAM format
vcf2adam : Convert a VCF file to the corresponding ADAM format
ADAM outputs all the commands that are available for you to run. To get
help for a specific command, run adam <command> -h, e.g.
$ adam transform --help
Argument "INPUT" is required
INPUT : The ADAM, BAM or SAM file to apply
the transforms to
OUTPUT : Location to write the transformed
data in ADAM/Parquet format
-coalesce N : Set the number of partitions written
to the ADAM output directory
-dbsnp_sites VAL : dbsnp sites file
-h (-help, --help, -?) : Print help
-mark_duplicate_reads : Mark duplicate reads
-parquet_block_size N : Parquet block size (default = 128mb)
-parquet_compression_codec [UNCOMPRESS : Parquet compression codec
ED | SNAPPY | GZIP | LZO] :
-parquet_disable_dictionary : Disable dictionary encoding
-parquet_page_size N : Parquet page size (default = 1mb)
-recalibrate_base_qualities : Recalibrate the base quality scores
(ILLUMINA only)
-sort_reads : Sort the reads by referenceId and
read position
-spark_env KEY=VALUE : Add Spark environment variable
-spark_home PATH : Spark home
-spark_jar JAR : Add Spark jar
-spark_master VAL : Spark Master (default = "local[#cores]
")
Once you have data converted to ADAM, you can gather statistics from the ADAM file using flagstat.
This command will output stats identically to the samtools flagstat command, e.g.
$ adam flagstat NA12878_chr20.adam
51554029 + 0 in total (QC-passed reads + QC-failed reads)
0 + 0 duplicates
50849935 + 0 mapped (98.63%:0.00%)
51554029 + 0 paired in sequencing
25778679 + 0 read1
25775350 + 0 read2
49874394 + 0 properly paired (96.74%:0.00%)
50145841 + 0 with itself and mate mapped
704094 + 0 singletons (1.37%:0.00%)
158721 + 0 with mate mapped to a different chr
105812 + 0 with mate mapped to a different chr (mapQ>=5)
In practice, you'll find that the ADAM flagstat command takes orders of magnitude less
time than samtools to compute these statistics. For example, on my MacBook Pro the command
above took 17 seconds to run while samtools flagstat NA12878_chr20.bam took 55 secs.
On larger files, the difference in speed is even more dramatic. ADAM is faster because
it's multi-threaded and distributed and uses a columnar storage format (with a projected
schema that only materializes the read flags instead of the whole read).
The ADAM mailing list is a good
way to sync up with other people who use ADAM including the core developers. You can subscribe
by sending an email to adam-developers+subscribe@googlegroups.com or just post using
the web forum page.
ADAM is released under an Apache 2.0 license.