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Job name
A valid submission name is required.
Choose a name for your submission.
Design sequences
Please provide a valid set of oligo sequences. They may only contain A, C, G, and T. At most 10000 sequences with up to 150 nucleotides each are allowed.
#oligos
0
max. length
0
avg. GC
0%
Random
Clear
Provide the oligo sequences for simulation. Enter each oligo on its own line. Limited to 10000 oligos of max. 150 nt each.
Synthesis
PCR
Aging
Sequencing
Synthesis platform
Electrochemical synthesis (e.g. Genscript)
Material deposition-based synthesis (e.g. Twist)
A valid synthesis platform is required.
Select the type of synthesis provider to be used.
Mean coverage
#
Mean synthesis coverage must be a positive integer.
Choose the mean number of oligos per sequence after synthesis.
Coverage homogeneity
Worst case
Best case
Valid synthesis homogeneity is required.
Choose the homogeneity of the coverage distribution after synthesis.
Polymerase
Taq-based (fidelity ~ 1)
Generic high fidelity (fidelity ~ 40)
Q5 HiFi (fidelity ~ 280)
exonuclease-deficient (fidelity ~ 0.3)
Choose a valid polymerase type.
Select the type of polymerase for the amplification.
Mean efficiency
%
Mean PCR efficiency must be between 50% and 100%.
Select the mean efficiency during amplification.
Efficiency distribution
Narrow
Wide
Valid efficiency bias is required.
Choose the homogeneity of the efficiency distribution.
Number of cycles
#
Number of PCR cycles must be between 0 and 120.
Total number of PCR cycles to simulate.
Simulate long-term storage
Choose whether to simulate decay during aging.
Choose whether to include aging in the simulation.
Initial coverage
#
Initial coverage must be between 1 and 200.
Choose the mean coverage just prior to aging.
Aging duration
τ
Number of half-lives must be between 0 and 10.
Select the extent of aging via the number of half-lives of decay.
Sequencing depth
#
Sequencing depth must be between 1 and 50.
Choose the mean number of reads per sequence during sequencing.
Read length
nt
Sequencing length must be between 30 and 300.
Select the read length during sequencing.
Paired reads
Choose whether to perform paired reads.
Choose whether paired reads are used during sequencing.
Error profile
Estimated from settings
Substitutions
PCR & Sequencing
1.2%
Deletions
Synthesis
1.2%
Insertions
negligible
0.0%
Coverage bias
Synthesis & PCR
0.53
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