GitHub / lvn3668 / naivevariantcaller_ECGR_variantdetection
Python code to detect ECGR Mutations; Takes a reference genome and bunch of reads as input and finds mutations (1-3 bp length) where number of supporting reads greater than 5
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PURL: pkg:github/lvn3668/naivevariantcaller_ECGR_variantdetection
Stars: 1
Forks: 0
Open issues: 0
License: None
Language: Python
Size: 2.39 MB
Dependencies parsed at: Pending
Created at: almost 4 years ago
Updated at: over 1 year ago
Pushed at: almost 4 years ago
Last synced at: over 1 year ago
Topics: bioinformatics-analysis, ecgr, genomics, ngs-analysis, python, reads, variant-calling