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Workflow Requirements

The minimum read length is 50 bases.
Each sample must have no more than 30 gigabases.
A minimum number of reads is not required. However, use sufficient data for each sample to support an appropriate depth of coverage for variant calling.
Each analysis uses only one manifest.
Samples are all paired-end or all single-end.
Sequenced samples have the same read lengths.
A maximum of 384 samples is possible per analysis.
AmpliSeq for Illumina DNA, RNA, and DNA + RNA Amplicon panels are supported.
For RNA Amplicon, only gene expression panels are supported. For differential expression, use the RNA Amplicon app.
Supports a maximum of 200 GB of sequence.