Use when downloading NCBI ASN.1 biological sequence archive divisions such as BCT, PLN, or VRL into the current directory.
原文语言:英语
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Use when downloading NCBI ASN.1 biological sequence archive divisions such as BCT, PLN, or VRL into the current directory.
原文语言:英语
Use when converting PubMed `DocumentSummary` XML into `Pubmed-entry` ASN.1 text, or into the intermediate XML form before final ASN.1 flattening.
原文语言:英语
Use when masking low-complexity regions in nucleotide sequences using the Symmetric DUST algorithm before BLAST searches or other sequence analyses.
原文语言:英语
Use when invoking the top-level `easel` dispatcher to discover or run Easel sequence-analysis subcommands from the HMMER toolchain.
原文语言:英语
Use when collecting sorted UID lists from EDirect query sources such as PubMed queries, explicit IDs, WebEnv history state, or input files.
原文语言:英语
Use when auditing or reusing the shared EDirect shell functions that other Entrez Direct wrapper scripts source internally.
原文语言:英语
Use when you need to fetch records or data from NCBI Entrez databases (PubMed, nucleotide, protein, gene, SRA, etc.) by ID or accession
原文语言:英语
Use when filtering Entrez search results by date, organism, publication type, sequence features, or other database-specific criteria in bioinformatics pipelines.
原文语言:英语
Use when you need to discover available NCBI Entrez databases, explore searchable fields within a specific database, or identify cross-database links for building EDirect queries.
原文语言:英语
Use when you need to navigate relationships between records in NCBI Entrez databases, find related articles, track citations, or link records across different databases such as PubMed to Protein.
原文语言:英语
Use when you need to post unique identifiers or accession numbers to NCBI Entrez databases for subsequent retrieval operations
原文语言:英语
Use when printing canned sample NCBI XML, JSON, flatfile, or GFF documents for testing, parser development, or xtract query prototyping.
原文语言:英语
Use when searching NCBI Entrez databases (pubmed, gene, protein, nuccore, snp, geoprofiles) with query strings and field qualifiers to retrieve record UIDs for downstream processing.
原文语言:英语
Use when retrieving specific multiple sequence alignments from an MSA file by name, or when indexing MSA files for faster access.
原文语言:英语
Use when manipulating multiple sequence alignment files using Easel tools from HMMER.
原文语言:英语
Use when comparing or mapping two multiple sequence alignments in Stockholm format to analyze their overlap or relationship.
原文语言:英语
Use when you need to mask columns in a multiple sequence alignment using gap frequencies, posterior probabilities, external mask files, or the RF annotation, or to truncate alignments to specific coordinate ranges.
原文语言:英语
Use when merging multiple sequence alignment files in Stockholm or Pfam format into a single alignment.
原文语言:英语
Use when calculating pairwise percent identities from multiple sequence alignments in FASTA or Stockholm format.
原文语言:英语
Use when you need to reverse sequences in a multiple sequence alignment file. Part of the Easel toolkit distributed with HMMER.
原文语言:英语
Use when working with alignment files and needing statistics from HMMER's Easel toolkit.
原文语言:英语
Use when comparing a test multiple sequence alignment against a trusted reference alignment to compute accuracy. Requires Stockholm format files with
原文语言:英语
Use when comparing two Stockholm format files with secondary structure markup to evaluate how well a test structure matches a trusted reference.
原文语言:英语
Use when inspecting, comparing, or rebuilding consensus RNA/DNA secondary-structure annotation in Stockholm alignments.
原文语言:英语
Use when turning one numeric value per line into Easel or xmgrace histogram or survival-plot data for score-distribution analysis.
原文语言:英语
Use when applying coordinate-based masks to named sequences in FASTA or other Easel-supported sequence files.
原文语言:英语
Use when fitting, scoring, generating, or sampling mixture Dirichlet priors for count-vector data used in HMMER or Infernal-style models.
原文语言:英语
Use when you need to convert sequence files between different formats such as FASTA, Stockholm, A2M, Clustal, or Phylip.
原文语言:英语
Use when reservoir-sampling a fixed number of random lines from a large text file or stream without loading the whole file.
原文语言:英语
Use when splitting an SSI-indexed sequence file into per-process sequence-index ranges for embarrassingly parallel Easel or HMMER jobs.
原文语言:英语
Use when you need to compute and report statistics on biological sequence files (e.g., count, length distribution, composition) as part of HMMER/Easel workflows.
原文语言:英语
Use when you need to extract specific sequences by name from a sequence file, or index a sequence file for faster lookup.
原文语言:英语
Use when shuffling biological sequences, bootstrapping alignment columns, or generating de novo random RNA, DNA, or protein controls.
原文语言:英语
Use when converting a Stockholm RNA or DNA alignment plus a PostScript structure template into colored secondary-structure diagrams.
原文语言:英语
Use when translating nucleotide sequences to amino acid sequences using Easel's translation utility from the HMMER suite.
原文语言:英语
Use when adding Stockholm sequence-weight annotations to nucleotide or protein MSAs before downstream HMMER-style modeling.
原文语言:英语
Use when fetching document summaries from NCBI Entrez databases by database name and identifier or accession
原文语言:英语
Use when working from the local Evo 2 repository for DNA-sequence scoring, embeddings, generation, or phage-genome design experiments.
原文语言:英语
Use when calling SNPs from aligned SAM/BAM reads with Subread's `exactSNP` variant caller.
原文语言:英语
Use when subtracting one Entrez or NCBI UID file from another and keeping only IDs unique to the first file.
原文语言:英语