High-performance toolkit for genomic interval analysis in Rust with Python bindings. Use when working with genomic regions, BED files, coverage tracks, overlap detection, tokenization for ML models, or fragment analysis in computational genomics and machine learning applications.
64
66%
Does it follow best practices?
Impact
32%
1.23xAverage score across 3 eval scenarios
Advisory
Suggest reviewing before use
Optimize this skill with Tessl
npx tessl skill review --optimize ./scientific-skills/gtars/SKILL.mdIGD overlap detection and RegionSet operations
Uses gtars import
0%
50%
IGD index build
0%
0%
IGD query method
0%
0%
IGD index persistence
0%
0%
RegionSet.from_bed usage
0%
25%
filter_overlapping method
0%
0%
Set operation usage
0%
0%
to_bed export
0%
100%
Overlap statistics
0%
0%
CLI IGD commands
0%
0%
Results documented
100%
100%
No large file warning
100%
100%
Coverage track generation and fragment processing
Uses gtars/gtars CLI
0%
57%
coverage_from_bed or gtars uniwig
0%
0%
BigWig format output
0%
0%
Resolution parameter
0%
0%
Fragment file format awareness
100%
80%
fragsplit filter command
0%
0%
fragsplit cluster-split command
0%
0%
Correct CLI argument syntax
0%
0%
Coverage output file produced
50%
75%
Workflow documentation
100%
85%
No large files
100%
100%
Genomic tokenization for ML preprocessing
TreeTokenizer import path
0%
0%
from_bed_file constructor
0%
0%
tokenize method signature
0%
0%
Batch tokenization loop
100%
100%
Token ID access
0%
0%
vocab_size usage
100%
100%
NumPy array export
0%
0%
RegionSet from_bed usage
0%
25%
geniml integration reference
0%
0%
Python API for pipeline
100%
100%
Token output file
100%
100%
No large files
100%
100%
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Table of Contents
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