
dna sequencing
GC bias and coverage holes
Extreme GC can look like a deletion. How polymerase and fragmentation leave coverage holes, and how a GC plot differs from a copy-number call.
8 October 2026 · 7 min read
Knowledge centre
Guides, method explainers and sourcing notes for research laboratories. Written by the EVRINTH Editorial Team from published methods, with catalogue links for enquiry rather than stock claims.
520 articles

dna sequencing
Extreme GC can look like a deletion. How polymerase and fragmentation leave coverage holes, and how a GC plot differs from a copy-number call.
8 October 2026 · 7 min read

gels and blotting
Save a gel image you can interpret: keep the ladder visible, avoid saturation, and do not let an overexposed no-template lane become a false positive.
8 October 2026 · 8 min read

gels and blotting
Compare a cut DNA band with a column cleanup: UV damage, carryover that blocks ligation, lower yield, and when not to slice.
8 October 2026 · 7 min read

cold chain
A short trip still needs the coolant the label names. Gel packs hold the setpoint they were conditioned to. Dry ice is a much colder window.
8 October 2026 · 9 min read

labware
How to specify a glass bottle and cap for steam sterilisation, including thread, headspace, loosened caps, and thermal shock.
8 October 2026 · 7 min read

laboratory safety
Dirty gloves, a rash at the cuff, and solvent wetting the skin are symptoms to reason about. Handwashing still belongs after the gloves come off.
8 October 2026 · 9 min read

molecular cloning
A glycerol freezer stock and a plasmid DNA tube fail in different ways. Use both when a thaw, a contaminated culture, or a mutant colony is the risk.
8 October 2026 · 8 min read

protein biochemistry
How a clonal glycerol stock fails: thawing the master, satellite colonies, and trusting an antibiotic plate instead of a sequence.
8 October 2026 · 8 min read

microbiology
How to freeze a verified E. coli clone in glycerol and revive it from the ice so the recovered colony is the one you archived.
8 October 2026 · 7 min read

molecular cloning
How type IIS enzymes such as BsaI or BbsI cut outside their site so designed overhangs assemble and the site is lost, compared with ligation and Gibson.
8 October 2026 · 8 min read

buffers and water
Good's buffers are a design family, not a procedure. Separate HEPES, MES, MOPS, and PIPES from metal binding, light reactions, and the pH you still measure.
8 October 2026 · 8 min read

chromatography
Choose an isocratic hold or a solvent gradient from the resolution you need, then budget dwell volume and column equilibration.
8 October 2026 · 7 min read