ADAM is a genomics analysis platform with specialized file formats built using Apache Avro, Apache Spark and Parquet. Apache 2 licensed.
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Latest commit 4c8ef3b Nov 27, 2016 @fnothaft fnothaft committed with heuermh [ADAM-1280] Silence CRAM logging in tests.
Resolves #1280.

README.md

ADAM

Introduction

ADAM is a genomics analysis platform with specialized file formats built using Apache Avro, Apache Spark and Apache Parquet. Apache 2 licensed. Some quick links:

Hello World: Counting K-mers

Here's an example ADAM CLI command that will count 10-mers in a test .sam file that lives in this repository:

$ adam-submit count_kmers /tmp/small.adam /tmp/kmers.adam 10
$ head /tmp/kmers.adam/part-*
(AATTGGCACT,1)
(TTCCGATTTT,1)
(GAGCAGCCTT,1)
(CCTGCTGTAT,1)
(TTTTAAGGTT,1)
(GGCCAGGACT,1)
(GCAGTCCCTC,1)
(AACTTTGAAT,1)
(GATGACGTGG,1)
(CTGTCCCTGT,1)

More than K-mer Counting

ADAM does much more than just k-mer counting. Running the ADAM CLI without arguments or with --help will display available commands, e.g.

$ adam-submit

       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

Usage: adam-submit [<spark-args> --] <adam-args>

Choose one of the following commands:

ADAM ACTIONS
               depth : Calculate the depth from a given ADAM file, at each variant in a VCF
         count_kmers : Counts the k-mers/q-mers from a read dataset.
  count_contig_kmers : Counts the k-mers/q-mers from a read dataset.
           transform : Convert SAM/BAM to ADAM format and optionally perform read pre-processing transformations
          adam2fastq : Convert BAM to FASTQ files
             flatten : Convert a ADAM format file to a version with a flattened schema, suitable for querying with tools like Impala
         mergeShards : Merges the shards of a file

CONVERSION OPERATIONS
            vcf2adam : Convert a VCF file to the corresponding ADAM format
            adam2vcf : Convert an ADAM variant to the VCF ADAM format
           anno2adam : Convert a annotation file (in VCF format) to the corresponding ADAM format
          fasta2adam : Converts a text FASTA sequence file into an ADAMNucleotideContig Parquet file which represents assembled sequences.
          adam2fasta : Convert ADAM nucleotide contig fragments to FASTA files
   transformFeatures : Convert a file with sequence features into corresponding ADAM format and vice versa
          wigfix2bed : Locally convert a wigFix file to BED format
     fragments2reads : Convert alignment records into fragment records.
     reads2fragments : Convert alignment records into fragment records.
      reads2coverage : Calculate the coverage from a given ADAM file

PRINT
               print : Print an ADAM formatted file
            flagstat : Print statistics on reads in an ADAM file (similar to samtools flagstat)
            listdict : Print the contents of an ADAM sequence dictionary
         allelecount : Calculate Allele frequencies
                view : View certain reads from an alignment-record file.

You can learn more about a command, by calling it without arguments or with --help, e.g.

$ adam-submit transform --help
 INPUT                                                           : The ADAM, BAM or SAM file to apply the transforms to
 OUTPUT                                                          : Location to write the transformed data in ADAM/Parquet format
 -add_md_tags VAL                                                : Add MD Tags to reads based on the FASTA (or equivalent) file passed to this option.
 -aligned_read_predicate                                         : Only load aligned reads. Only works for Parquet files.
 -cache                                                          : Cache data to avoid recomputing between stages.
 -coalesce N                                                     : Set the number of partitions written to the ADAM output directory
 -concat VAL                                                     : Concatenate this file with <INPUT> and write the result to <OUTPUT>
 -defer_merging                                                  : Defers merging single file output
 -dump_observations VAL                                          : Local path to dump BQSR observations to. Outputs CSV format.
 -force_load_bam                                                 : Forces Transform to load from BAM/SAM.
 -force_load_fastq                                               : Forces Transform to load from unpaired FASTQ.
 -force_load_ifastq                                              : Forces Transform to load from interleaved FASTQ.
 -force_load_parquet                                             : Forces Transform to load from Parquet.
 -force_shuffle_coalesce                                         : Even if the repartitioned RDD has fewer partitions, force a shuffle.
 -h (-help, --help, -?)                                          : Print help
 -known_indels VAL                                               : VCF file including locations of known INDELs. If none is provided, default
                                                                   consensus model will be used.
 -known_snps VAL                                                 : Sites-only VCF giving location of known SNPs
 -limit_projection                                               : Only project necessary fields. Only works for Parquet files.
 -log_odds_threshold N                                           : The log-odds threshold for accepting a realignment. Default value is 5.0.
 -mark_duplicate_reads                                           : Mark duplicate reads
 -max_consensus_number N                                         : The maximum number of consensus to try realigning a target region to. Default
                                                                   value is 30.
 -max_indel_size N                                               : The maximum length of an INDEL to realign to. Default value is 500.
 -max_target_size N                                              : The maximum length of a target region to attempt realigning. Default length is
                                                                   3000.
 -md_tag_fragment_size N                                         : When adding MD tags to reads, load the reference in fragments of this size.
 -md_tag_overwrite                                               : When adding MD tags to reads, overwrite existing incorrect tags.
 -paired_fastq VAL                                               : When converting two (paired) FASTQ files to ADAM, pass the path to the second file
                                                                   here.
 -parquet_block_size N                                           : Parquet block size (default = 128mb)
 -parquet_compression_codec [UNCOMPRESSED | SNAPPY | GZIP | LZO] : Parquet compression codec
 -parquet_disable_dictionary                                     : Disable dictionary encoding
 -parquet_logging_level VAL                                      : Parquet logging level (default = severe)
 -parquet_page_size N                                            : Parquet page size (default = 1mb)
 -print_metrics                                                  : Print metrics to the log on completion
 -realign_indels                                                 : Locally realign indels present in reads.
 -recalibrate_base_qualities                                     : Recalibrate the base quality scores (ILLUMINA only)
 -record_group VAL                                               : Set converted FASTQs' record-group names to this value; if empty-string is passed,
                                                                   use the basename of the input file, minus the extension.
 -repartition N                                                  : Set the number of partitions to map data to
 -single                                                         : Saves OUTPUT as single file
 -sort_fastq_output                                              : Sets whether to sort the FASTQ output, if saving as FASTQ. False by default.
                                                                   Ignored if not saving as FASTQ.
 -sort_lexicographically                                         : Sort the reads lexicographically by contig name, instead of by index.
 -sort_reads                                                     : Sort the reads by referenceId and read position
 -storage_level VAL                                              : Set the storage level to use for caching.
 -stringency VAL                                                 : Stringency level for various checks; can be SILENT, LENIENT, or STRICT. Defaults
                                                                   to LENIENT

The ADAM transform command allows you to mark duplicates, run base quality score recalibration (BQSR) and other pre-processing steps on your data.

Getting Started

Installation

Binary Distributions

Bundled release binaries can be found on our releases page.

Building from Source

You will need to have Maven installed in order to build ADAM.

Note: The default configuration is for Hadoop 2.6.0. If building against a different version of Hadoop, please edit the build configuration in the <properties> section of the pom.xml file.

$ git clone https://github.com/bigdatagenomics/adam.git
$ cd adam
$ export MAVEN_OPTS="-Xmx512m -XX:MaxPermSize=256m"
$ mvn clean package -DskipTests
...
[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] ------------------------------------------------------------------------

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.

Installing Spark

You'll need to have a Spark release on your system and the $SPARK_HOME environment variable pointing at it; prebuilt binaries can be downloaded from the Spark website. Currently, our continuous builds default to Spark 1.6.1 built against Hadoop 2.6, but any more recent Spark distribution should also work.

Helpful Aliases

You might want to add the following to your .bashrc to make running ADAM easier:

alias adam-submit="${ADAM_HOME}/bin/adam-submit"
alias adam-shell="${ADAM_HOME}/bin/adam-shell"

$ADAM_HOME should be the path to a binary release or a clone of this repository on your local filesystem.

These aliases call scripts that wrap the spark-submit and spark-shell commands to set up ADAM.Once they are in place, you can run adam by simply typing adam-submit at the command line, as demonstrated above.

Running ADAM

Now you can try running some simple ADAM commands:

transform

Make your first .adam file like this:

adam-submit transform $ADAM_HOME/adam-core/src/test/resources/small.sam /tmp/small.adam

If you didn't obtain your copy of adam from github, you can grab small.sam here.

flagstat

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.

If you followed along above, now try gathering some statistics:

$ adam-submit flagstat /tmp/small.adam
20 + 0 in total (QC-passed reads + QC-failed reads)
0 + 0 primary duplicates
0 + 0 primary duplicates - both read and mate mapped
0 + 0 primary duplicates - only read mapped
0 + 0 primary duplicates - cross chromosome
0 + 0 secondary duplicates
0 + 0 secondary duplicates - both read and mate mapped
0 + 0 secondary duplicates - only read mapped
0 + 0 secondary duplicates - cross chromosome
20 + 0 mapped (100.00%:0.00%)
0 + 0 paired in sequencing
0 + 0 read1
0 + 0 read2
0 + 0 properly paired (0.00%:0.00%)
0 + 0 with itself and mate mapped
0 + 0 singletons (0.00%:0.00%)
0 + 0 with mate mapped to a different chr
0 + 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 a MacBook Pro flagstat NA12878_chr20.bam took 17 seconds to run while samtools flagstat NA12878_chr20.bam took 55 seconds. 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).

adam-shell

The adam-shell command opens an interpreter that you can run ad-hoc ADAM commands in.

For example, the following code snippet will generate a result similar to the k-mer-counting example above, but with the k-mers sorted in descending order of their number of occurrences. To use this, save the code snippet as kmer.scala and run adam-shell -i kmer.scala.

kmer.scala

import org.bdgenomics.adam.rdd.ADAMContext._
import org.bdgenomics.adam.projections.{ AlignmentRecordField, Projection }

// Load alignments from disk
val reads = sc.loadAlignments(
  "/data/NA21144.chrom11.ILLUMINA.adam",
  projection = Some(
    Projection(
      AlignmentRecordField.sequence,
      AlignmentRecordField.readMapped,
      AlignmentRecordField.mapq
    )
  )
)

// Generate, count and sort 21-mers
val kmers =
  reads
    .rdd
    .flatMap(_.getSequence.sliding(21).map(k => (k, 1L)))
    .reduceByKey(_ + _)
    .map(_.swap)
    .sortByKey(ascending = false)

// Print the top 10 most common 21-mers
kmers.take(10).foreach(println)

adam-shell -i kmer.scala

$ adam-shell -i kmer.scala
…
(121771,TTTTTTTTTTTTTTTTTTTTT)
(44317,ACACACACACACACACACACA)
(44023,TGTGTGTGTGTGTGTGTGTGT)
(42474,CACACACACACACACACACAC)
(42095,GTGTGTGTGTGTGTGTGTGTG)
(33797,TAATCCCAGCACTTTGGGAGG)
(33081,AATCCCAGCACTTTGGGAGGC)
(32775,TGTAATCCCAGCACTTTGGGA)
(32484,CCTCCCAAAGTGCTGGGATTA)
…

Running on a cluster

The adam-submit and adam-shell commands can also be used to submit ADAM jobs to a Spark cluster, or to run ADAM interactively. Cluster mode can be enabled by passing the same flags you'd pass to Spark, e.g. --master yarn --deploy-mode client.

Under the Hood

ADAM relies on several open-source technologies to make genomic analyses fast and massively parallelizable…

Apache Spark

Apache Spark allows developers to write algorithms in succinct code that can run fast locally, on an in-house cluster or on Amazon, Google or Microsoft clouds.

Apache Parquet

Apache Parquet is a columnar storage format available to any project in the Hadoop ecosystem, regardless of the choice of data processing framework, data model or programming language.

  • Parquet compresses legacy genomic formats using standard columnar techniques (e.g. RLE, dictionary encoding). ADAM files are typically ~20% smaller than compressed BAM files.
  • Parquet integrates with:
    • Query engines: Hive, Impala, HAWQ, IBM Big SQL, Drill, Tajo, Pig, Presto
    • Frameworks: Spark, MapReduce, Cascading, Crunch, Scalding, Kite
    • Data models: Avro, Thrift, ProtocolBuffers, POJOs
  • Parquet is simply a file format which makes it easy to sync and share data using tools like distcp, rsync, etc
  • Parquet provides a command-line tool, parquet.hadoop.PrintFooter, which reports useful compression statistics

In the counting k-mers example above, you can see there is a defined predicate and projection. The predicate allows rapid filtering of rows while a projection allows you to efficiently materialize only specific columns for analysis. For this k-mer counting example, we filter out any records that are not mapped or have a MAPQ less than 20 using a predicate and only materialize the Sequence, ReadMapped flag and MAPQ columns and skip over all other fields like Reference or Start position, e.g.

Sequence ReadMapped MAPQ Reference Start ...
GGTCCAT false - chrom1 - ...
TACTGAA true 30 chrom1 34232 ...
TTGAATG true 17 chrom1 309403 ...

Apache Avro

Our Avro schemas are directly converted into source code using Avro tools. 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.

Downstream Applications

There are a number of projects built on ADAM, e.g.

  • RNAdam provides an RNA pipeline on top of ADAM with isoform quantification and fusion transcription detection
  • Avocado is a variant caller built on top of ADAM for germline and somatic calling
  • PacMin is an assembler for PacBio reads
  • A Mutect port is nearly feature complete
  • Read error correction
  • a graphing and genome visualization library
  • BDG-Services is a library for accessing a running Spark cluster through web-services or a Thrift- interface
  • Short read assembly
  • Variant filtration (train model via MLlib)

License

ADAM is released under an Apache 2.0 license.