io
FastqReaderProcess
¶
Bases: Process
Reads fastq file(s) in chunks and places them on a queue.
Attributes:
Name | Type | Description |
---|---|---|
input_file |
Input fastq files. |
|
outq |
Output queue for chunked reads/read pairs. |
|
statq |
(Not currently used) Queue for read statistics if required. |
|
read_buffer |
Number of reads to process before placing them on outq |
|
read_counter |
(Not currently used) Can be used to sync between multiple readers. |
|
n_subproceses |
Number of processes running concurrently. Used to make sure enough termination signals are used. |
Source code in capcruncher/api/io.py
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run()
¶
Performs reading and chunking of fastq file(s).
Source code in capcruncher/api/io.py
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bam_to_parquet(bam, output)
¶
Converts bam file to parquet file.
Parameters:
Name | Type | Description | Default |
---|---|---|---|
bam |
Union[str, Path]
|
Path to bam file. |
required |
output |
Union[str, Path]
|
Path to output parquet file. |
required |
Source code in capcruncher/api/io.py
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parse_alignment(aln)
¶
Parses reads from a bam file into a list.
Extracts
-read name -parent reads -flashed status -slice number -mapped status -multimapping status -chromosome number (e.g. chr10) -start (e.g. 1000) -end (e.g. 2000) -coords e.g. (chr10:1000-2000)
Parameters:
Name | Type | Description | Default |
---|---|---|---|
aln |
AlignmentFile
|
pysam.AlignmentFile. |
required |
Returns: list: Containing the attributes extracted.
Source code in capcruncher/api/io.py
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parse_bam(bam)
¶
Uses parse_alignment function convert bam file to a dataframe.
Extracts
-'slice_name' -'parent_read' -'pe' -'slice' -'mapped' -'multimapped' -'chrom' -'start' -'end' -'coordinates'
Parameters:
Name | Type | Description | Default |
---|---|---|---|
bam |
Union[str, Path]
|
Path to bam file. |
required |
Returns:
Type | Description |
---|---|
DataFrame
|
pd.Dataframe: DataFrame with the columns listed above. |
Source code in capcruncher/api/io.py
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