org.bdgenomics.adam.rdd.variant
Called genotypes.
A dictionary describing the reference genome.
The samples called.
The VCF header lines that cover all INFO/FORMAT fields needed to represent this RDD of Genotypes.
Performs a broadcast inner join between this RDD and another RDD.
Performs a broadcast inner join between this RDD and another RDD.
In a broadcast join, the left RDD (this RDD) is collected to the driver, and broadcast to all the nodes in the cluster. The key equality function used for this join is the reference region overlap function. Since this is an inner join, all values who do not overlap a value from the other RDD are dropped.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space.
Performs a broadcast inner join between this RDD and another RDD.
Performs a broadcast inner join between this RDD and another RDD.
In a broadcast join, the left RDD (this RDD) is collected to the driver, and broadcast to all the nodes in the cluster. The key equality function used for this join is the reference region overlap function. Since this is an inner join, all values who do not overlap a value from the other RDD are dropped.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space.
Runs a filter that selects data in the underlying RDD that overlaps a single genomic region.
Runs a filter that selects data in the underlying RDD that overlaps a single genomic region.
The region to query for.
Returns a new GenomicRDD containing only data that overlaps the query region.
Runs a filter that selects data in the underlying RDD that overlaps several genomic regions.
Runs a filter that selects data in the underlying RDD that overlaps several genomic regions.
The regions to query for.
Returns a new GenomicRDD containing only data that overlaps the querys region.
Performs a sort-merge full outer join between this RDD and another RDD.
Performs a sort-merge full outer join between this RDD and another RDD.
In a sort-merge join, both RDDs are co-partitioned and sorted. The
partitions are then zipped, and we do a merge join on each partition.
The key equality function used for this join is the reference region
overlap function. Since this is a full outer join, if a value from either
RDD does not overlap any values in the other RDD, it will be paired with
a None in the product of the join.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that
overlapped in the genomic coordinate space, and values that did not
overlap will be paired with a None.
The genotype to get a reference region for.
Returns the singular region this genotype covers.
The VCF header lines that cover all INFO/FORMAT fields needed to represent this RDD of Genotypes.
The VCF header lines that cover all INFO/FORMAT fields needed to represent this RDD of Genotypes.
The underlying RDD of genomic data, as a JavaRDD.
The underlying RDD of genomic data, as a JavaRDD.
Performs a sort-merge left outer join between this RDD and another RDD.
Performs a sort-merge left outer join between this RDD and another RDD.
In a sort-merge join, both RDDs are co-partitioned and sorted. The
partitions are then zipped, and we do a merge join on each partition.
The key equality function used for this join is the reference region
overlap function. Since this is a left outer join, all values in the
right RDD that do not overlap a value from the left RDD are dropped.
If a value from the left RDD does not overlap any values in the right
RDD, it will be paired with a None in the product of the join.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space, and all keys from the left RDD that did not overlap a key in the right RDD.
Pipes genomic data to a subprocess that runs in parallel using Spark.
Pipes genomic data to a subprocess that runs in parallel using Spark.
Files are substituted in to the command with a $x syntax. E.g., to invoke a command that uses the first file from the files Seq, use $0.
Pipes require the presence of an InFormatterCompanion and an OutFormatter as implicit values. The InFormatterCompanion should be a singleton whose apply method builds an InFormatter given a specific type of GenomicRDD. The implicit InFormatterCompanion yields an InFormatter which is used to format the input to the pipe, and the implicit OutFormatter is used to parse the output from the pipe.
The type of the record created by the piped command.
A GenomicRDD containing X's.
The InFormatter to use for formatting the data being piped to the command.
Command to run.
Files to make locally available to the commands being run. Default is empty.
A map containing environment variable/value pairs to set in the environment for the newly created process. Default is empty.
Number of bases to flank each command invocation by.
Returns a new GenomicRDD of type Y.
Called genotypes.
Called genotypes.
An RDD to replace the underlying RDD with.
Returns a new GenotypeRDD with the underlying RDD replaced.
Performs a broadcast right outer join between this RDD and another RDD.
Performs a broadcast right outer join between this RDD and another RDD.
In a broadcast join, the left RDD (this RDD) is collected to the driver,
and broadcast to all the nodes in the cluster. The key equality function
used for this join is the reference region overlap function. Since this
is a right outer join, all values in the left RDD that do not overlap a
value from the right RDD are dropped. If a value from the right RDD does
not overlap any values in the left RDD, it will be paired with a None
in the product of the join.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space, and all keys from the right RDD that did not overlap a key in the left RDD.
Performs a broadcast right outer join between this RDD and another RDD.
Performs a broadcast right outer join between this RDD and another RDD.
In a broadcast join, the left RDD (this RDD) is collected to the driver,
and broadcast to all the nodes in the cluster. The key equality function
used for this join is the reference region overlap function. Since this
is a right outer join, all values in the left RDD that do not overlap a
value from the right RDD are dropped. If a value from the right RDD does
not overlap any values in the left RDD, it will be paired with a None
in the product of the join.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space, and all keys from the right RDD that did not overlap a key in the left RDD.
Performs a sort-merge right outer join between this RDD and another RDD.
Performs a sort-merge right outer join between this RDD and another RDD.
In a sort-merge join, both RDDs are co-partitioned and sorted. The
partitions are then zipped, and we do a merge join on each partition.
The key equality function used for this join is the reference region
overlap function. Since this is a right outer join, all values in the
left RDD that do not overlap a value from the right RDD are dropped.
If a value from the right RDD does not overlap any values in the left
RDD, it will be paired with a None in the product of the join.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space, and all keys from the right RDD that did not overlap a key in the left RDD.
Performs a sort-merge right outer join between this RDD and another RDD, followed by a groupBy on the left value, if not null.
Performs a sort-merge right outer join between this RDD and another RDD, followed by a groupBy on the left value, if not null.
In a sort-merge join, both RDDs are co-partitioned and sorted. The
partitions are then zipped, and we do a merge join on each partition.
The key equality function used for this join is the reference region
overlap function. In the same operation, we group all values by the left
item in the RDD. Since this is a right outer join, all values from the
right RDD who did not overlap a value from the left RDD are placed into
a length-1 Iterable with a None key.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space, grouped together by the value they overlapped in the left RDD, and all values from the right RDD that did not overlap an item in the left RDD.
The samples called.
The samples called.
Automatically detects the extension and saves to either VCF or Parquet.
Automatically detects the extension and saves to either VCF or Parquet.
Arguments configuring how to save the output.
Java-friendly method for saving.
Java-friendly method for saving.
Path to save file to. If ends in ".vcf", saves as VCF, else saves as Parquet.
Saves this RDD to disk as a Parquet file.
Saves this RDD to disk as a Parquet file.
Path to save the file at.
Saves this RDD to disk as a Parquet file.
Saves this RDD to disk as a Parquet file.
Path to save the file at.
Size per block.
Size per page.
Name of the compression codec to use.
Whether or not to disable bit-packing.
Saves this RDD to disk as a Parquet file.
Saves this RDD to disk as a Parquet file.
Path to save the file at.
Size per block.
Size per page.
Name of the compression codec to use.
Whether or not to disable bit-packing. Default is false.
Saves RDD as a directory of Parquet files.
Saves RDD as a directory of Parquet files.
The RDD is written as a directory of Parquet files, with Parquet configuration described by the input param args. The provided sequence dictionary is written at args.outputPath/_seqdict.avro as Avro binary.
Save configuration arguments.
Explicitly saves to VCF.
Explicitly saves to VCF.
The filepath to save to.
If true, saves the output as a single file by merging the sharded output after completing the write to HDFS. If false, the output of this call will be written as shards, where each shard has a valid VCF header.
The validation stringency to use when writing the VCF.
Explicitly saves to VCF.
Explicitly saves to VCF.
Arguments configuring how/where to save the output.
Whether to sort when saving or not.
Saves Avro data to a Hadoop file system.
Saves Avro data to a Hadoop file system.
This method uses a SparkContext to identify our underlying file system, which we then save to.
Frustratingly enough, although all records generated by the Avro IDL compiler have a static SCHEMA$ field, this field does not belong to the SpecificRecordBase abstract class, or the SpecificRecord interface. As such, we must force the user to pass in the schema.
The type of the specific record we are saving.
Path to save records to.
SparkContext used for identifying underlying file system.
Schema of records we are saving.
Seq of records we are saving.
Called in saveAsParquet after saving RDD to Parquet to save metadata.
Called in saveAsParquet after saving RDD to Parquet to save metadata.
Writes any necessary metadata to disk. If not overridden, writes the sequence dictionary to disk as Avro.
Saves an RDD of Avro data to Parquet.
Saves an RDD of Avro data to Parquet.
The path to save the file to.
The size in bytes of blocks to write.
The size in bytes of pages to write.
The compression codec to apply to pages.
If false, dictionary encoding is used. If true, delta encoding is used.
The schema to set.
A dictionary describing the reference genome.
A dictionary describing the reference genome.
Performs a sort-merge inner join between this RDD and another RDD.
Performs a sort-merge inner join between this RDD and another RDD.
In a sort-merge join, both RDDs are co-partitioned and sorted. The partitions are then zipped, and we do a merge join on each partition. The key equality function used for this join is the reference region overlap function. Since this is an inner join, all values who do not overlap a value from the other RDD are dropped.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space.
Performs a sort-merge inner join between this RDD and another RDD, followed by a groupBy on the left value.
Performs a sort-merge inner join between this RDD and another RDD, followed by a groupBy on the left value.
In a sort-merge join, both RDDs are co-partitioned and sorted. The partitions are then zipped, and we do a merge join on each partition. The key equality function used for this join is the reference region overlap function. Since this is an inner join, all values who do not overlap a value from the other RDD are dropped. In the same operation, we group all values by the left item in the RDD.
The right RDD in the join.
Returns a new genomic RDD containing all pairs of keys that overlapped in the genomic coordinate space, grouped together by the value they overlapped in the left RDD..
Sorts our genome aligned data by reference positions, with contigs ordered by index.
Sorts our genome aligned data by reference positions, with contigs ordered by index.
Returns a new RDD containing sorted data.
Does not support data that is unaligned or where objects align to multiple positions.
sortLexicographically
Sorts our genome aligned data by reference positions, with contigs ordered lexicographically.
Sorts our genome aligned data by reference positions, with contigs ordered lexicographically.
Returns a new RDD containing sorted data.
Does not support data that is unaligned or where objects align to multiple positions.
sort
Returns this GenotypeRDD squared off as a VariantContextRDD.
Applies a function that transforms the underlying RDD into a new RDD.
Applies a function that transforms the underlying RDD into a new RDD.
A function that transforms the underlying RDD.
A new RDD where the RDD of genomic data has been replaced, but the metadata (sequence dictionary, and etc) is copied without modification.
An RDD containing genotypes called in a set of samples against a given reference genome.
Called genotypes.
A dictionary describing the reference genome.
The samples called.
The VCF header lines that cover all INFO/FORMAT fields needed to represent this RDD of Genotypes.