TacoSkill LAB
TacoSkill LAB
HomeSkillHubCreatePlaygroundSkillKit
© 2026 TacoSkill LAB
AboutPrivacyTerms
  1. Home
  2. /
  3. SkillHub
  4. /
  5. pysam
Improve

pysam

8.3

by K-Dense-AI

138Favorites
357Upvotes
0Downvotes

Genomic file toolkit. Read/write SAM/BAM/CRAM alignments, VCF/BCF variants, FASTA/FASTQ sequences, extract regions, calculate coverage, for NGS data processing pipelines.

genomics

8.3

Rating

0

Installs

Data & Analytics

Category

Quick Review

Excellent bioinformatics skill with comprehensive coverage of pysam's genomic file processing capabilities. The SKILL.md provides clear, actionable guidance with strong quick-start examples and well-organized references for alignment, variant, and sequence file operations. The description is sufficiently detailed for CLI invocation, covering when to use the skill and core operations. Task knowledge is outstanding with referenced documentation for all major workflows. Structure is exemplary—concise main file with detailed references properly separated. Novelty is strong: genomic file manipulation with coordinate systems, indexing requirements, and multi-format integration would consume significant tokens and require specialized domain knowledge for a CLI agent. Minor room for improvement in the description's specificity about edge cases, but overall this is a highly practical, well-documented skill that meaningfully reduces complexity for NGS data processing tasks.

LLM Signals

Description coverage9
Task knowledge10
Structure10
Novelty8

GitHub Signals

6,871
818
49
3
Last commit 1 days ago

Publisher

K-Dense-AI

K-Dense-AI

Skill Author

Related Skills

spark-engineerpandas-proxlsx

Loading SKILL.md…

Try onlineView on GitHub

Publisher

K-Dense-AI avatar
K-Dense-AI

Skill Author

Related Skills

spark-engineer

Jeffallan

6.4

pandas-pro

Jeffallan

6.4

xlsx

mrgoonie

7.2

infographic-syntax-creator

antvis

6.8
Try online