Determine the
appropriate
Illumina NGS/
microarray
solutions
Define project
scope and
sample
requirements
Review
logistics and
timelines
Prepare sample
for sequencing
or array
scanning
Perform sample
and/or library
QC
Sequence or
scan samples
Analyse
samples with
BaseSpace™
Sequence Hub
or Illumina
genotyping
software
Review
personalized
workflow and
generated data
Transfer data
using
BasSpace™
Sequence Hub
Discuss
implementation
When to use?
Establishing an optimized sample-to-answer workflow
is critical during the implementation and startup phase
of integrating new NGS or microarray technology.
With the Illumina Workflow Design and Evaluation
Service, researchers can evaluate workflows using
their own samples with expert support to accelerate
the journey towards successful genomics research.
For Research Use Only. Not for use in diagnostic procedures.