Basecall ONT POD5 with Dorado, align with Minimap2, assemble with Flye/Hifiasm, call SVs with Sniffles2. Use when basecalling nanopore reads, doing long-read assembly, SV calling, or ONT methylation/isoform analysis.
Parse LC-MS mzML with pyOpenMS, PQN/LOESS-normalize feature tables, match m/z to HMDB/GNPS by ppm, run COBRApy FBA. Use when doing metabolomics preprocessing, metabolite ID, feature QC, MSEA enrichment, or flux modeling.
Run Bowtie2 decontamination, Kraken2/Bracken classification, HUMAnN3 pathways, and MEGAHIT/MetaBAT2/CheckM MAG recovery on shotgun metagenomes. Use for WMS/WGS metagenomics, microbiome profiling, or MAG binning.
Build PPI networks from STRING with NetworkX, find hub genes via centrality, detect Louvain modules, infer GRNs with GENIE3. Use for protein interaction networks, hub/bottleneck genes, network communities, GRN inference.
Detect and correct for population stratification and cryptic relatedness in genotype data using PCA, kinship/IBD estimation, and genomic inflation factor (lambda) diagnostics before running a GWAS. Use when doing ancestry PCA, checking sample relatedness, computing genomic inflation, or QC'ing genotype data for…
Embed proteins with ESM2, predict structure via ESMFold, zero-shot score mutations with ESM-1v, or design sequences via ESM-IF1 (fair-esm). Use for protein embeddings, MSA-free structure, DMS/VUS scoring, fixed-backbone design.
Write Python decorators/context managers/dataclasses and query gene/variant tables with sqlite3/pandas SQL (JOIN, GROUP BY, HAVING). Use for retry/caching/validation wrappers or SQL against Ensembl/UCSC-style schemas.
Build Python classes for Gene/DNA/RNA/Protein records with eq/lt/hash, @property validation, ABCs, and @classmethod parsers (fromfastastring). Use when modeling genes/FASTA/GFF as objects or asked about Python OOP, inheritance, dataclasses.
Build Python context managers (enter/exit, @contextmanager, sqlite3) for safe FASTA I/O, temp cleanup, DB transactions. Use for leaked file handles, temp files surviving crashes, or with-compatible readers/writers.
Write if/elif/for/while loops over DNA/RNA/protein strings: codon iteration, stop-codon/motif scanning, GC-content classification. Use when looping over sequences, extracting codons, or debugging an off-by-one loop.
Use Python's int, float, str, bool, and None types to represent and validate biological data (sequence lengths, GC content, DNA/RNA strings, missing annotations) and convert between them when parsing text records. Use when writing beginner Python for bioinformatics, explaining type() output, fixing float-equality bugs…
Build volcano/MA plots, clustermap heatmaps, and multi-panel GridSpec figures with matplotlib/seaborn. Use when plotting DE results, expression data, or QC distributions, or fixing savefig, log-axis, colormap bugs.
Write @decorators (functools.wraps, @lrucache, factories) to time, validate, and memoize bio functions. Use for pipeline timing/logging, DNA/protein alphabet checks, caching codon/alignment calls, or decorator stacking.
Use Python dict/defaultdict/Counter/set to translate codons, count k-mers, group genes by chromosome, and compare gene lists (union/intersection). Use when translating DNA, counting k-mers, or comparing gene sets.
Handle malformed FASTA/GFF via try/except/else/finally, custom exceptions, raise-from chaining. Use for parsers crashing on bad input, strict vs lenient FASTA parsing, KeyError/IndexError/ValueError, or batches skipping bad records.
Use Python arithmetic and comparison operators to compute GC content, codon/frame math, protein MW, and primer Tm. Use when calculating GC%, codon counts, reading frames, or fixing operator-precedence bugs in bio scripts.
Read/write FASTA, FASTQ, CSV/TSV (BED), JSON, and pickle files in Python using open()/context managers, csv.DictReader/DictWriter, and streaming generators for large genomics files. Use when parsing a FASTA/FASTQ file, writing sequences back out with line wrapping, reading/writing gene expression CSV or BED/TSV files…
Write Python def functions for bio scripts — ORF finders, reverse-complement, Hamming distance, args/kwargs, @lrucache. Use for a mutable-default-argument bug, args/kwargs signatures, or reusable sequence helpers.
Write Python generators (yield, itertools) for streaming FASTA/FASTQ readers, sliding-window GC/k-mer scans, and lazy translation pipelines that skip loading whole files into memory. Use for large FASTA/FASTQ parsing or MemoryError on genomic data.
Stream FASTA/FASTQ and generate k-mers/codons lazily with Python generators, custom iter/next classes, and itertools. Use when parsing multi-GB sequence files without loading them fully into RAM or chaining filter-trim-translate pipelines.
Split CDS into codons, extract k-mers, sort sequences by GC%/length, and pack gene coordinates into tuples/namedtuples. Use when looping over genes/codons/SNPs/BED intervals, computing sliding-window GC%, or detecting gene overlaps in Python.
★not rated 5 2mo agoA63 tokens
At most 3 mods per repository are shown here, and a mod shipped inside a plugin is left to that plugin's page — the rest are on their repository pages: