Use when converting BLAST/genomic-map alignment summaries into compact strand-and-range tables for later interval fusion.
原文语言:英语
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Use when converting BLAST/genomic-map alignment summaries into compact strand-and-range tables for later interval fusion.
原文语言:英语
Use when converting BLASTN mRNA alignment XML into segmented interval reports and strand-overlap summaries in EDirect pipelines.
原文语言:英语
Use when you need to summarize tabular data by grouping rows on common column values and applying aggregation operations (sum, count, mean, etc.), similar to SQL GROUP BY.
原文语言:英语
Use when plotting `bcftools +guess-ploidy -v` output into a PNG summary of haploid, diploid, score, and site-count signals across samples.
原文语言:英语
Use when converting EDirect HGVS XML records into NCBI SPDI XML, optionally with a precomputed accession-to-CDS-offset transform table.
原文语言:英语
Use when aligning RNA-seq reads to a reference genome using a HISAT2 index, particularly for splice-aware alignment of transcriptomic data.
原文语言:英语
Use when aligning RNA-seq reads to a HISAT2 index using the alignment binary directly. Supports spliced alignment with optional splice site annotation.
原文语言:英语
Use when building large HISAT2 index files from reference sequences for RNA-seq alignment with splice-aware mapping support.
原文语言:英语
Use when building a HISAT2 graph-based index from reference sequences for splice-aware RNA-seq alignment, optionally incorporating SNPs, haplotypes, splice sites, or exon annotations.
原文语言:英语
Use when building HISAT2 index files from reference genomes for subsequent alignment with hisat2. Handles FASTA reference inputs and creates .ht2 index files.
原文语言:英语
Use when extracting exon coordinates from GTF annotation files for HISAT2 index building or splice-aware alignment preparation.
原文语言:英语
Use when extracting SNPs and haplotypes from UCSC SNP files for HISAT2 graph-based genome indexing.
原文语言:英语
Use when extracting SNPs and haplotypes from VCF files to build variant-aware HISAT2 graph genome indexes
原文语言:英语
Use when extracting splice junctions from GTF annotation files for HISAT2 splice-aware alignment.
原文语言:英语
Use when you need to inspect or extract information from HISAT2 large index files (.ht2l), including reference sequences, splice sites, SNPs, exons, or index summaries.
原文语言:英语
Use when extracting metadata, reference names, SNPs, splice sites, or exon information from HISAT2 index files (.ht2).
原文语言:英语
Use when you need to inspect HISAT2 index files, extract reference sequences, view index summaries, or retrieve SNP/splice site/exon information from a .ht2 index.
原文语言:英语
Use when you need to compute basic read statistics (count, min/max/average length) from FASTQ/FASTA files before or after HISAT2 alignment workflows.
原文语言:英语
Use when simulating RNA-seq or DNA-seq reads from a reference genome and GTF annotation file, optionally incorporating SNP variants and controlling expression profiles.
原文语言:英语
Use when aligning RNA-seq reads to a reference genome using graph-based indexing for fast and sensitive spliced alignment.
原文语言:英语
Use when aligning sequences to a profile HMM to produce multiple sequence alignments.
原文语言:英语
Use when turning curated multiple-sequence alignments into profile HMM files for HMMER search or database-preparation workflows.
原文语言:英语
Use when converting profile HMM files between HMMER3 ASCII or binary, legacy HMMER2, or specific 3.x text revisions.
原文语言:英语
Use when sampling synthetic sequences, alignments, or consensus sequences from one or more profile HMMs.
原文语言:英语
Use when you need to extract specific HMM profiles from an HMM database file by name, or index an HMM file for faster lookups.
原文语言:英语
Use when extracting per-position residue-height and indel-rate data from a profile HMM for sequence-logo visualization.
原文语言:英语
Use when running the sharded `hmmpgmd_shard` daemon so large protein sequence databases are split across HMMER worker nodes.
原文语言:英语
Use when running HMMER master or worker daemon services that front `phmmer`, `hmmsearch`, and `hmmscan` against cached databases.
原文语言:英语
Use when preparing profile HMM databases for use with hmmpgmd (HMMER daemon) by creating compressed binary index files.
原文语言:英语
Use when searching protein sequences against profile hidden Markov models (HMMs) such as Pfam or other HMM databases.
原文语言:英语
Use when searching profile hidden Markov models against sequence databases to identify homologous sequences or protein family members
原文语言:英语
Use when you need to characterize score distributions of a profile HMM on random sequences, such as calibration checks, benchmarking, or filter-behavior experiments.
原文语言:英语
Use when you need to inspect and summarize statistics for HMM (profile hidden Markov model) files from the HMMER suite.
原文语言:英语
Use when you need to identify, view, or copy HTS-format files (BAM, CRAM, VCF, BCF). Use for inspecting file headers or viewing textual representations of binary HTS files.
原文语言:英语
Use when converting INI-style configuration files into XML for downstream EDirect or XML-based processing.
原文语言:英语
Use when deriving interpolated per-base coverage counts from a sorted SAM file, especially across paired-end inserts.
原文语言:英语
Use when you need to find overlaps between two genomic interval files (BED, GFF, VCF, or BAM), filter features by intersection, or count/report overlapping regions between datasets.
原文语言:英语
Use when keeping only the Entrez or NCBI UIDs present in both of two UID files.
原文语言:英语
Use when inferring maximum-likelihood phylogenies from aligned sequences, performing automated model selection, or assessing branch support with bootstrap or aLRT methods
原文语言:英语
Use when inferring maximum-likelihood phylogenetic trees, selecting substitution models, running bootstrap support analyses, or performing partitioned phylogenetic analyses on sequence alignments.
原文语言:英语