SpikeForge

known variants and fusions, planted into real data

Create research-use synthetic controls from BAM or FASTQ files, then verify exactly what changed. Choose one sample below or validate a CSV plan for a cohort.

!
Research use only — not for diagnosis, treatment selection, or patient care. Keep the original sequencing files unchanged. SpikeForge outputs are synthetic positive controls and must not enter clinical reporting.
Choose a local path or an HTTPS download link. Linked BAMs download to this computer before processing; SpikeForge never uploads them.

1 Input

Where is the input BAM?
Only files beneath the data folder selected when SpikeForge started are available.
A new BAM is written here. The original BAM is never used as the output.
A substitution in a BAM can be checked from its MD tags when no FASTA is supplied.

2 What to plant

“Add ALT reads” asks for additional edited BAM records. Mates and duplicate families remain together, so the nearest biologically coherent count may differ.

3 Run

Verification is on by default. Review achieved read count/VAF and all warnings before using the control.

Result

Nothing run yet.

Choose a local file or folder