跳到正文
cccskills
免费在 GitHub 公开

bio-rna-quantification-featurecounts-counting

Count reads per gene from aligned BAM files using Subread featureCounts. Use when processing BAM files from STAR/HISAT2 to generate gene-level counts for DESeq2/edgeR.

中文简介正在准备中。当前显示原文说明。

查看安装方法

包含的文件(4)

  • SKILL.md5.4 KB
  • examples/count_genes.sh643 B
  • examples/process_counts.py719 B
  • usage-guide.md3.8 KB

SKILL.md(原文)

安装前可以查看交给 AI 代理的指令内容。

Version Compatibility

Reference examples tested with: DESeq2 1.42+, HISAT2 2.2.1+, STAR 2.7.11+, Subread 2.0+, edgeR 4.0+, pandas 2.2+, scanpy 1.10+

Before using code patterns, verify installed versions match. If versions differ:

  • Python: pip show <package> then help(module.function) to check signatures
  • R: packageVersion('<pkg>') then ?function_name to verify parameters
  • CLI: <tool> --version then <tool> --help to confirm flags

If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.

featureCounts Counting

"Count reads per gene from my BAM files" → Assign aligned reads to genomic features using a GTF annotation to produce a gene-by-sample count matrix for DE analysis.

  • CLI: featureCounts -a genes.gtf -o counts.txt sample1.bam sample2.bam

Count reads mapping to genomic features (genes, exons) from BAM files.

Basic Usage

# Single sample
featureCounts -a annotation.gtf -o counts.txt aligned.bam

# Multiple samples (recommended - single matrix output)
featureCounts -a annotation.gtf -o counts.txt sample1.bam sample2.bam sample3.bam

# All BAMs in directory
featureCounts -a annotation.gtf -o counts.txt *.bam

Paired-End Data

# Count fragments, not reads (required for paired-end)
featureCounts -p --countReadPairs -a annotation.gtf -o counts.txt *.bam

# Check proper pairs only
featureCounts -p --countReadPairs -B -C -a annotation.gtf -o counts.txt *.bam

Flags:

  • -p - Input is paired-end
  • --countReadPairs - Count fragments instead of reads
  • -B - Only count properly paired reads
  • -C - Don't count chimeric fragments

Strand-Specific Libraries

# Unstranded (default)
featureCounts -s 0 -a annotation.gtf -o counts.txt *.bam

# Forward stranded (e.g., dUTP, NSR)
featureCounts -s 1 -a annotation.gtf -o counts.txt *.bam

# Reverse stranded (e.g., Illumina TruSeq, most common)
featureCounts -s 2 -a annotation.gtf -o counts.txt *.bam

Determining strandedness: Use infer_experiment.py from RSeQC or check library prep protocol.

Feature Types

# Count at gene level (default)
featureCounts -t exon -g gene_id -a annotation.gtf -o counts.txt *.bam

# Count at transcript level
featureCounts -t exon -g transcript_id -a annotation.gtf -o counts.txt *.bam

# Count CDS only
featureCounts -t CDS -g gene_id -a annotation.gtf -o counts.txt *.bam

Flags:

  • -t - Feature type in GTF (default: exon)
  • -g - Meta-feature attribute (default: gene_id)

Multi-Mapping Reads

# Discard multi-mappers (default, recommended for DE)
featureCounts -a annotation.gtf -o counts.txt *.bam

# Count multi-mappers (fractional)
featureCounts -M --fraction -a annotation.gtf -o counts.txt *.bam

# Count multi-mappers (full count to each location)
featureCounts -M -a annotation.gtf -o counts.txt *.bam

Overlapping Features

# Discard reads overlapping multiple features (default)
featureCounts -a annotation.gtf -o counts.txt *.bam

# Count reads overlapping multiple features
featureCounts -O -a annotation.gtf -o counts.txt *.bam

# Fractional count for overlaps
featureCounts -O --fraction -a annotation.gtf -o counts.txt *.bam

Performance Options

# Use multiple threads
featureCounts -T 8 -a annotation.gtf -o counts.txt *.bam

# Use less memory (slower)
featureCounts --largeBAM -a annotation.gtf -o counts.txt *.bam

Output Files

featureCounts produces two files:

  1. counts.txt - Main count matrix
Geneid  Chr     Start   End     Strand  Length  sample1.bam  sample2.bam
GENE1   chr1    100     500     +       400     1523         1891
GENE2   chr1    1000    2000    -       1000    892          756
  1. counts.txt.summary - Assignment statistics
Status                  sample1.bam  sample2.bam
Assigned                1523456      1678234
Unassigned_Unmapped     12345        11234
Unassigned_NoFeatures   234567       245678

Extract Count Matrix

# Remove first 6 columns (metadata) to get just counts
cut -f1,7- counts.txt | tail -n +2 > count_matrix.txt

Python Processing

import pandas as pd

counts = pd.read_csv('counts.txt', sep='\t', comment='#')
count_matrix = counts.set_index('Geneid').iloc[:, 5:]  # Skip metadata columns
count_matrix.columns = [c.replace('.bam', '') for c in count_matrix.columns]
count_matrix.to_csv('count_matrix.csv')

R Processing

counts <- read.table('counts.txt', header=TRUE, row.names=1, skip=1)
count_matrix <- counts[, 6:ncol(counts)]  # Skip metadata columns
colnames(count_matrix) <- gsub('.bam', '', colnames(count_matrix))

Common Issues

Low assignment rate:

  • Check strandedness setting (-s)
  • Verify GTF matches reference genome version
  • Check BAM alignment quality

Zero counts for known expressed genes:

  • Ensure feature type matches GTF (-t exon vs -t gene)
  • Check gene_id attribute name in GTF

Related Skills

  • alignment-files/sam-bam-basics - Input BAM file handling
  • genome-intervals/gtf-gff-handling - GTF annotation files
  • differential-expression/deseq2-basics - Downstream analysis with counts
  • rna-quantification/count-matrix-qc - QC of count data

评价

还没有评价。欢迎分享你的使用感受。

评论

无需登录即可发表。欢迎分享使用感受、提问,或说明在哪些环境下无法运行。

还没有评论。来写第一条吧。

提交后会立即公开。请勿填写邮箱、电话等个人信息。URL 最多 2 个。

0 / 1000 字

此表单受 reCAPTCHA 保护,适用 Google 的隐私权政策和服务条款。

同一仓库的技能

Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

alphafold

免费

Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

atac-seq

免费

ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

bindcraft

免费

End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.

中文简介正在准备中。当前显示原文说明。

BioTender-max/awesome-bio-agent-skills2042026年7月2日 更新

查看 BioTender-max 的全部技能

报告此技能的问题