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9 search results found

Benchmarking Tools ⭐ 110

Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls

Grenepipe ⭐ 75

A flexible, scalable, and reproducible pipeline to automate variant calling from sequence reads.

Teamteri ⭐ 50

Genomics (computational bioinformatic data analysis) running on GCP, AWS or Azure

🔧 Simple script in python to convert CSV files to VCF

Seqarray ⭐ 41

Data management of large-scale whole-genome sequence variant calls (Development version only)

Starfish ⭐ 17

Intersect multiple VCF files with haplotype awareness

Umccrise ⭐ 14

🐍 DRAGEN Tumor/Normal workflow post-processing

Pyseqarray ⭐ 12

PySeqArray: data manipulation of whole-genome sequencing variants with SeqArray files in Python (pre-release version)

Genericlistcpp ⭐ 6

An implementation of a generic ArrayList and a generic LinkedList in cpp which can store multiple data type variables.

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1-9 of 9 search results

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