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Pipeline run errors

Use this reference to identify and resolve errors that occur when the Emedgene pipeline processes a case. Each entry includes the numeric error code, the exception name, and a description of the likely cause and recommended corrective action.

When a pipeline run fails, the error code is shown on the case card and in the case details. Locate the code in the relevant section below to understand the cause and next step. If the code is not listed, or if the issue persists, contact Illumina Technical Support with the error code, the case ID, and any relevant logs.


Error code ranges

Code range
Category

6XXX

Pipeline exceptions

8XXX

Infrastructure-related exceptions

9XXX

Sanity check exceptions

10XXX

Input-related exceptions (detailed below)


Input errors

These errors occur when case inputs — such as sample type, phenotypes, reference genome, or kit BED file — are missing, conflicting, or invalid.

Code
Exception
Description

10001

InputValidationException

One or more input fields failed validation. Check that all required case fields are filled in correctly before resubmitting.

10002

MissingInputFilesException

Expected input files were not found in the specified location. Verify that all files are accessible at the provided paths.

10003

FileNotFoundException

A required file could not be located. Confirm the file path is correct and that the file exists in the configured storage.

10004

BadPosException

A genomic position in the input is invalid or out of range for the reference genome.

10005

BadRefException

A reference allele in the input does not match the configured reference genome.

10006

MalformedTestDataException

The test data provided for the case is malformed or does not meet the expected format.

10007

NoneSampleTypeException

No sample type was specified. A sample type is required to run the pipeline.

10008

TooManyPhenotypesException

The number of phenotypes submitted exceeds the supported limit.

10009

NoSampleNameGivenException

A sample was submitted without a name. All samples must have a unique identifier.

10010

UnsupportedReference

The reference genome specified is not supported. See Supported reference genome assemblies for valid options.

10011

ReferenceConflictException

The input files reference conflicting genome assemblies. All files in a case must use the same reference genome.

10012

MissingKitBedException

A kit BED file is required for this case type but was not provided.

10013

UnknownHaplotypeException

A haplotype specified in the input is not recognized by the pipeline.

10014

HaplotypeAlleleAmountMismatchException

The number of alleles specified for a haplotype does not match the expected count.


File errors

These errors indicate a problem with a submitted file — it may be corrupted, empty, or unsorted.

Code
Exception
Description

10101

CorruptedFileException

A file could not be read because its contents are corrupted. Re-upload the file and resubmit.

10102

CorruptedGzipFileException

A gzip-compressed file is corrupted or was not compressed correctly. Re-compress and re-upload the file.

10103

EmptyFileException

A required file was found but contains no data. Ensure the correct non-empty file was uploaded.

10104

UnsortedInputFileException

An input file is not sorted in the required order. Sort the file by chromosome and position before resubmitting.

10105

EmptyRemoteFileException

A file retrieved from remote storage returned no data. Check that the file exists and is not empty at the remote location.


VCF errors

These errors are raised when the pipeline parses the VCF file and encounters structural problems, missing headers, unrecognized variant callers, or allele mismatches.

Code
Exception
Description

10201

CorruptedVcfException

The VCF file is corrupted and cannot be parsed. Validate the file with a VCF linter and re-upload.

10202

NoContigsException

The VCF header is missing contig definitions. Add ##contig lines for all chromosomes referenced in the file.

10203

NoTitleException

The VCF is missing the required #CHROM header line.

10204

NoVcfVersionException

The VCF header does not specify a file format version (##fileformat). Add a valid ##fileformat line.

10205

NoVariantsFound

The VCF file contains no variant records. Confirm the correct file was uploaded.

10206

UnsupportedVcfVersionException

The VCF format version is not supported. See Supported variant callers for compatible formats.

10207

ConflictingVariantTypesException

The VCF contains variants of conflicting types that cannot be processed together in a single run.

10208

SampleNameNotFoundInVcfException

The sample name specified for the case was not found in the VCF header. Verify the sample name matches exactly.

10209

MoreThanOneVarCallerMatched

The VCF matches more than one supported variant caller profile. Ensure the file originates from a single caller.

10210

CorruptedVariantException

One or more variant records in the VCF are malformed or missing required fields.

10211

CorruptedSVVariantException

One or more structural variant records are malformed. Check SV-specific fields such as SVTYPE and END.

10212

MissingVcfColumnException

A required VCF column is absent. Ensure the file includes all mandatory columns (CHROM, POS, ID, REF, ALT, QUAL, FILTER, INFO).

10213

NoEmedgenizerException

The pipeline could not identify the variant caller as a supported one for this VCF.

10214

ReferenceAlleleMismatchException

The REF allele in the VCF does not match the reference genome at the specified position.

10215

NoJSONEmedgenizerException

No compatible JSON-based variant caller annotation tool was identified for this VCF.


VCF line errors

These errors occur at the individual record level within a VCF file — malformed lines, missing fields, or ambiguous variant type annotations.

Code
Exception
Description

10301

CorruptedLineException

A line in the VCF file is malformed and could not be parsed. Check for encoding issues or unexpected characters.

10302

CorruptedHeaderException

A header line in the VCF is malformed. Validate all ##INFO, ##FORMAT, and ##FILTER header definitions.

10303

EmptyLineException

An unexpected empty line was found in the VCF body. Remove blank lines from within the file.

10304

MissingAltException

A variant record is missing the ALT allele field. All variants must have at least one ALT value.

10306

UnfinishedLineException

A line in the VCF appears truncated. The file may have been interrupted during upload or compression.

10307

MoreThanOneVariantTypeMatchedException

A single VCF line matched more than one variant type. Ensure variant records have unambiguous type annotations.

10308

CorruptedSampleColumnException

A sample column in the VCF is corrupted or does not match the FORMAT definition.

10309

CorruptedFormatForSampleException

The FORMAT field for a sample column is invalid or does not conform to the declared FORMAT header.

10310

InfinityVcfException

A numeric field in the VCF contains an infinity value, which is not permitted.

10311

MoreThanOneJSONVarCallerMatched

More than one JSON-based variant caller matched in this json line.


FASTQ errors

This error indicates a problem with a submitted FASTQ file.

Code
Exception
Description

10401

CorruptedFastqException

The FASTQ file is corrupted and cannot be parsed. Validate the file and re-upload a complete, intact copy.

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