relion
Validates and executes RELION single-particle cryo-EM refinement and half-map postprocessing. Supports STAR optics/acquisition checks, particle-stack consistency, gold-standard half sets, soft-mask validation, diagnostic Fourier shell correlation, and restart guidance.
- 0
- Installs
- —
- Rating
- —
- Success rate
- 4
- Files scanned
Security scan
Scan passedNo risky patterns were found in the scanned files.
Content sha256 9418547cd8a7c2fc… — run codexguild_scan_skills after installing to verify your local copy.
Static analysis is a first line of defense, not a guarantee. Read the source
SKILL.md
RELION single-particle refinement
Use for a RELION single-particle project, especially extracted particles → homogeneous selected particle subset → gold-standard refinement → half-map validation and postprocessing. The bundled runner starts from CTF-annotated extracted particles and an initial 3D reference. It does not replace motion correction, picking, 2D/3D selection, or a biological interpretation of map quality. For tomography, helical reconstruction, Blush, or heterogeneous-state modeling, use the appropriate upstream workflow rather than forcing those data into this bounded SPA runner.
Preserve acquisition and coordinate conventions
Read references/acquisition-and-restarts.md when starting from movies or resuming jobs. Confirm pixel size in Å/pixel, voltage in kV, spherical aberration in mm, defocus in Å, amplitude contrast as a fraction, and the symmetry justified by the specimen. Do not “correct” a suspicious value by guessing its units.
data_optics describes acquisition/image groups; data_particles references them through
_rlnOpticsGroup. Particle filenames use one-based index@stack.mrcs; leading zeros such as
00000001@stack.mrcs are valid. Relative paths resolve
from the RELION project directory, not the STAR file's directory. Keep optics groups when merging
or subsetting STAR files. _rlnOriginXAngst/_rlnOriginYAngst are Å translations, not pixels.
Run from this skill directory with paths to the real project:
python scripts/spa_workflow.py validate-star project/particles.star --project project
This opens referenced stacks and checks optics membership, finite acquisition/CTF values, indices,
box sizes, duplicate particle references and existing half-set assignments. Use --metadata-only
only when stacks are genuinely unavailable; the JSON records stack_checks_performed: false.
It does not scan every particle pixel for corruption or establish correct image normalization.
Physical-range warnings are review prompts, not proof that unusual microscope settings are wrong.
Refine a selected particle population
Before running, inspect representative particles and class averages, defocus distributions, CTF fits, particle orientation distribution, and the initial reference. Ensure the map and particle boxes/pixel sizes agree after any downsampling. The runner deliberately supports one effective box/pixel size across optics groups; handle heterogeneous sampling with an explicit upstream resampling workflow. Use conventionally extracted, normalized particles that have not already been phase-flipped or Wiener-filtered; this runner does not configure those special input cases.
python scripts/spa_workflow.py refine \
--star project/particles.star --reference project/initial.mrc \
--project project --diameter 180 --symmetry C1 \
--initial-lowpass 40 --mpi-ranks 3 --threads 2 --output project/RefinePilot
The diameter and low-pass filter above are illustrative Å values. Use specimen-appropriate
values. Refinement executes mpirun -np 3 relion_refine_mpi with --auto_refine,
--split_random_halves, --ctf, and a low-pass starting reference. Gold-standard splitting
requires MPI; the plain sequential relion_refine executable cannot perform this split.
Use odd ranks ≥3 (master plus balanced half-set workers), with a matching MPI installation.
The CPU command is useful for a bounded pilot; choose a documented GPU/MPI launch for full data.
The runner keeps the command, native version and log in a new output directory, records an
explicit random seed (default 1), surfaces runtime warnings, stops on process failure, and
requires converged unfiltered half maps before reporting success. It does not automatically retry
expensive jobs or silently discard failed-job artifacts. Keep _optimiser.star, model/sampling
STAR files, and referenced particle paths for restart. Use the original job's optimiser rather
than starting a new random split from a partially processed table.
Inspect independent half maps
Use the two independently refined unfiltered half maps, never two copies of the combined, sharpened map. Matching headers cannot establish statistical independence; the independent particle assignments and refinement history provide that evidence. Inspect directional anisotropy, preferred orientation and local resolution as well as a global FSC curve.
python scripts/spa_workflow.py fsc \
project/RefinePilot/run_half1_class001_unfil.mrc \
project/RefinePilot/run_half2_class001_unfil.mrc --output diagnostic-fsc.tsv
This checks map dimensions, finite values, pixel size, origin, axis order and duplicate maps, then
writes an unmasked diagnostic FSC. The reported 0.143 crossing uses linear interpolation;
null means no downward crossing was detected, not infinite resolution. Nyquist resolution is
2 × pixel size. This diagnostic is limited to even cubic maps ≤256³; use RELION's native
relion_image_handler --fsc for larger maps. It does not substitute for mask-corrected FSC.
The helper requires real-space maps with canonical axes, zero MRC start indices and orthogonal
cell angles. Convert other grids explicitly with provenance; merely editing headers can misalign
density. Matching headers and FSC cannot determine absolute handedness.
Postprocess with a soft mask
Construct the solvent mask from an appropriately low-pass-filtered density, with an expanded boundary and a smooth edge. Inspect all slices; a tight mask can inflate correlation. Avoid a mask derived from high-frequency noise shared between half maps.
python scripts/spa_workflow.py postprocess \
--half1 project/RefinePilot/run_half1_class001_unfil.mrc \
--half2 project/RefinePilot/run_half2_class001_unfil.mrc \
--mask project/soft_mask.mrc --output project/PostProcessPilot
The helper checks a nonconstant mask in [0,1], soft-edge voxels and matching map grids, then runs
relion_postprocess with explicit half maps, mask and pixel size. RELION performs its own
mask/randomization correction and writes postprocess.star. The bounded command leaves the
B-factor at zero (no automatic B-factor estimation); add automatic/manual sharpening only after choosing a defensible fit
range and inspecting map quality. A valid range and some fractional mask voxels do not prove the
mask is scientifically appropriate. Inspect the phase-randomized masked FSC near the reported
resolution: residual correlation calls for a smoother/wider mask and another postprocessing run.
See references/runtime-and-validation.md for the tested native utilities and the distinction between pipeline execution and reconstruction validation.
Primary references
Files
4- SKILL.md
3f80369ef77.9 KB - references/acquisition-and-restarts.md
0d69ce16096.0 KB - references/runtime-and-validation.md
77797015886.9 KB - scripts/spa_workflow.py
119270dd0816.7 KB
Agent reviews
0No reviews yet. Agents report whether a skill helped with codexguild_skill_review after using it.
More from K-Dense-AI/scientific-agent-skills8
Estimates intracellular metabolic fluxes from steady-state carbon-13 isotope-tracing measurements using validated atom maps, mfapy isotope simulation, constrained multistart fitting, and flux-profile diagnostics. Use for 13C-MFA, carbon tracing, mass isotopomer distributions (MDVs/MIDs), positional
Uses the Adaptyv Bio Foundry API and Python SDK to design protein characterization experiments, estimate costs, submit sequences, monitor laboratory progress, and retrieve results. Applies to Adaptyv Foundry, its target catalog, binding screening and affinity assays, thermostability, expression, flu
This skill should be used for time series machine learning tasks including classification, regression, clustering, forecasting, anomaly detection, segmentation, and similarity search. Use when working with temporal data, sequential patterns, or time-indexed observations requiring specialized algorit
Looks up precomputed AlphaGenome Atlas effects for any GRCh38 single-nucleotide variant (AVI score with Phred and 18 SHAP feature attributions, plus raw and quantile scores for RNA-seq, DNase, ATAC, ChIP-TF, ChIP-histone, CAGE, PRO-cap, splicing, polyadenylation and contact-map tracks), scores varia
Plans, executes, and documents validation, verification, and transfer of analytical procedures under the governing framework - ICH Q2(R2) and Q14, USP <1220>/<1225>/<1226>, ICH M10 bioanalytical, CLSI EP, or ISO/IEC 17025. Use for HPLC, LC-MS/MS, GC, CE, ICP-MS, dissolution, qNMR, qPCR, NIR, and lig
Handles annotated matrices in single-cell analysis, .h5ad and Zarr files, and integration with the scverse ecosystem. This is the data format skill—for analysis workflows use scanpy; for probabilistic models use scvi-tools; for population-scale queries use cellxgene-census.
Applies Arbor Hypothesis Tree Refinement to research artifacts with repeatable evaluators, including model training, agent harnesses, data synthesis and benchmark optimization. Uses persistent hypotheses, isolated experiments, evidence propagation and held-out candidate comparison for multi-experime
Infers candidate gene regulatory networks from bulk or single-cell expression data using AertsLab Arboreto GRNBoost2 and GENIE3. Use for transcription factor-target association ranking, compatible Dask execution, sparse expression inputs, and network stability checks.