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Troubleshooting Articles
Molecular Biology
Molecular Biology
Is there a way to set the plasmid topology during new entity registration?
Is Data Entered into Benchling's AlphaFold Tool Secure?
What is the difference between the nucleotide or protein match type?
Why are my reads not aligning in sequential order anymore?
Why is there an "Invalid link" error on my part links?
Why is my "Genome" dropdown menu greyed out or missing options?
How do I change the natural analogue of an existing monomer in the Monomer Library?
How do I link translations for DNA sequences with alternative start codons?
How can I back translate AA sequences in bulk?
Why is the "Change Amino Acid" option on my sequence greyed out?
Why can I no longer see the assembly history in the lineage tab?
Why did the uridine content increase in my sequence?
Why are Benchling-generated canonical SMILES different from other SMILES?
Why can’t I generate Primers using the Benchling Primer Wizard for certain genes?
Can I attach more than 300 existing primers to a sequence?
Why is my Molecular Biology toolbar on the left side and not the right side?
Why are there extra amino acids in the amino acid list?
Why are my DNA sequence bases upper and lowercase after importing DNA sequences?
Why is my Benchling DNA sequence name not the same as the name of the file I imported?
Why am I receiving an error when importing a .gb DNA sequence?
How do I search for an archived entry or entity?
Does Benchling accept degenerate bases for DNA sequences?
How can I copy and paste my sequence with annotations?
Can I bulk unlink parts from multiple sequences?
Why is my sequence not auto-reindexing when I realign?
Are higher or lower CRISPR gRNA off-target scores better?
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