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databases bioinformatics AI 技能

发现 databases bioinformatics 相关 Skills,比较来源仓库和用途,查看适合你工作流的技能说明。

分类目录: databases bioinformatics

显示第 217–240 个,共 920 个

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GitHub

bio-microbiome-taxonomy-assignment

GPTomics

Taxonomic classification of ASVs using reference databases like SILVA, GTDB, or UNITE. Covers naive Bayes classifiers (DADA2, IDTAXA) and exact matching approaches. Use when assigning taxonomy to ASVs after DAD...

GitHub

bio-atac-seq-nucleosome-positioning

GPTomics

Extract nucleosome positions from ATAC-seq data using NucleoATAC, ATACseqQC, and fragment analysis. Use when analyzing chromatin organization, identifying nucleosome-free regions at promoters, or characterizing...

GitHub

bio-proteomics-proteomics-qc

GPTomics

Quality control and assessment for proteomics data. Covers sample quality metrics, missing value patterns, replicate correlation, batch effect detection, and intensity distribution checks.

GitHub

bio-crispr-batch-correction

GPTomics

Batch effect correction for CRISPR screens. Covers normalization across batches, technical replicate handling, and batch-aware analysis. Use when combining screens from multiple batches or correcting systematic...

GitHub

bio-workflows-atacseq-pipeline

GPTomics

End-to-end ATAC-seq workflow from FASTQ files to differential accessibility and TF footprinting. Covers alignment, peak calling with MACS3, QC metrics, and optional TOBIAS footprinting.

GitHub

bio-population-genetics-association-testing

GPTomics

Genome-wide association studies (GWAS) with PLINK. Perform case-control and quantitative trait association testing using logistic/linear regression with covariates, generate Manhattan and QQ plots for result vi...

GitHub

bio-phasing-imputation-imputation-qc

GPTomics

Quality control of phasing and imputation results. Filter by INFO scores, assess accuracy, and prepare imputed data for downstream analysis. Use when filtering low-quality imputed variants or validating imputat...

GitHub

bio-variant-calling

GPTomics

Call SNPs and indels from aligned reads using bcftools mpileup and call. Use when detecting variants from BAM files or generating VCF from alignments.

GitHub

bio-workflows-multi-omics-pipeline

GPTomics

End-to-end multi-omics integration workflow. Orchestrates data harmonization, MOFA/mixOmics integration, factor interpretation, and downstream analysis across transcriptomics, proteomics, metabolomics, and othe...

GitHub

bio-flow-cytometry-clustering-phenotyping

GPTomics

Unsupervised clustering and cell type identification for flow/mass cytometry. Covers FlowSOM, Phenograph, and CATALYST workflows. Use when discovering cell populations in high-dimensional cytometry data without...

GitHub

bio-alignment-statistics

GPTomics

Generate alignment statistics using samtools flagstat, stats, depth, and coverage. Use when assessing alignment quality, calculating coverage, or generating QC reports.

GitHub

bio-longread-medaka

GPTomics

Polish assemblies and call variants from Oxford Nanopore data using medaka. Uses neural networks trained on specific basecaller versions. Use when improving ONT-only assemblies or calling variants from Nanopore...

GitHub

bio-phasing-imputation-reference-panels

GPTomics

Download, prepare, and manage reference panels for phasing and imputation. Covers 1000 Genomes, HRC, and TOPMed panels. Use when setting up imputation infrastructure or selecting appropriate reference panels fo...

GitHub

bio-read-qc-fastp-workflow

GPTomics

All-in-one read preprocessing with fastp including adapter trimming, quality filtering, deduplication, base correction, and HTML report generation. Use when preprocessing Illumina data and wanting a single fast...

GitHub

bio-alignment-filtering

GPTomics

Filter alignments by flags, mapping quality, and regions using samtools view and pysam. Use when extracting specific reads, removing low-quality alignments, or subsetting to target regions.

GitHub

bio-reference-operations

GPTomics

Generate consensus sequences and manage reference files using samtools. Use when creating consensus from alignments, indexing references, or creating sequence dictionaries.

GitHub

bio-imc-interactive-annotation

GPTomics

Interactive cell type annotation for IMC data. Covers napari-based annotation, marker-guided labeling, training data generation, and annotation validation. Use when manually annotating cell types for training c...

GitHub

bio-methylation-dmr-detection

GPTomics

Differentially methylated region (DMR) detection using methylKit tiles, bsseq BSmooth, and DMRcate. Use when identifying contiguous genomic regions with methylation differences between experimental conditions o...

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